
Soluções e Reagentes da Farmacopeia dos Estados Unidos (USP)
As soluções e reagentes da Farmacopeia dos Estados Unidos (USP) são cruciais para garantir a segurança, qualidade e eficácia dos produtos farmacêuticos no mercado dos EUA. Esses produtos cumprem os padrões estabelecidos pela USP e são amplamente utilizados no desenvolvimento de medicamentos e no controle de qualidade. Na CymitQuimica, oferecemos uma ampla gama de soluções e reagentes em conformidade com a USP para apoiar a pesquisa e fabricação farmacêutica.
Foram encontrados 7603 produtos de "Soluções e Reagentes da Farmacopeia dos Estados Unidos (USP)"
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Reagecon Sulfuric Acid 1.00N Solution according to United States Pharmacopoeia (USP)
Reagecon's Sulfuric Acid 1.00N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Sulphuric Acid 0.5N in Alcohol according to United States Pharmacopoeia (USP)
Reagecon's Sulphuric Acid 0.5N in Alcohol is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Stock Solution to make Arsenic Trioxide according to United States Pharmacopoeia (USP)
Reagecon's Stock Solution to make Arsenic Trioxide according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Dichlorofluorescein TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Dichlorofluorescein TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Resorcinol TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Resorcinol TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Iodine 0.05N according to United States Pharmacopoeia (USP)
Reagecon's Iodine 0.05N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Matching Fluid H according to United States Pharmacopoeia (USP)
Reagecon's Matching Fluid H according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. Has guaranteed stability throughout its entire shelf life, even after opening the bottle.Cor e Forma:LiquidReagecon Oxalic Acid TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Oxalic Acid TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Zinc Sulphate 0.1M according to United States Pharmacopoeia (USP)
CAS:Reagecon's Zinc Sulphate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Iodine 0.01N according to United States Pharmacopoeia (USP)
Reagecon's Iodine 0.01N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Dichlorofluorescein TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Dichlorofluorescein TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Sodium Thiosulphate 0.100N (N/10) according to United States Pharmacopoeia (USP)
Reagecon's Sodium Thiosulphate 0.100N (N/10) is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Ammonia (Ammonium Hydroxide) TS Solution according to United States Pharmacopoeia (USP)
CAS:Reagecon's Ammonia (Ammonium Hydroxide) TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Methyl Red TS 2 conforms to United States Pharmacopoeia (USP)
Reagecon's Methyl Red TS 2 Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator, titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's’s facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Cor e Forma:LiquidReagecon Diluted Alcohol (50/50 Alcohol Water) Solution according to United States Pharmacopoeia (USP)
Reagecon's Diluted Alcohol (50/50 Alcohol Water) Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Glycerin Base TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Glycerin Base TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Cupric Sulfate TS Solution according to United States Pharmacopoeia (USP)
CAS:Reagecon's Cupric Sulfate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon pH 6.80 Monobasic Potassium Phosphate/Dibasic Sodium Phosphate Buffered Eluent in accordance with United States Pharmacopoeia (USP)
Reagecon's pH 6.8 Monobasic Potassium Phosphate/Dibasic Sodium Phosphate Buffered Eluent is tested, is NIST traceable and has guaranteed stability throughout its entire shelf life, even after opening the bottle. The product is developed, formulated and specified in accordance with United States Pharmacopoeia (USP) requirements.Cor e Forma:LiquidReagecon Ferric Chloride TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Ferric Chloride TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Perchloric Acid 0.1N in Glacial Acetic Acid according to United States Pharmacopoeia (USP)
Reagecon's Perchloric Acid 0.1N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Barium Nitrate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Barium Nitrate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Ammonium Chloride TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Ammonium Chloride TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Hydrochloric Acid Dilute Solution according to United States Pharmacopoeia (USP)
Reagecon's Hydrochloric Acid Dilute Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Iodine (Iodine-Iodide) 0.100N Solution according to United States Pharmacopoeia (USP)
Reagecon's Iodine (Iodine-Iodide) 0.100N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Cupric Acetate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Cupric Acetate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Potassium Hydroxide Alcoholic 0.5N according to United States Pharmacopoeia (USP)
Reagecon's Potassium Hydroxide Alcoholic 0.5N according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Edetate DiSodium TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Edetate DiSodium TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Sodium Acetate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Sodium Acetate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Ferric Ammonium Sulfate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Ferric Ammonium Sulfate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Matching Fluid A according to United States Pharmacopoeia (USP)
Reagecon's Matching Fluid A according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. Has guaranteed stability throughout its entire shelf life, even after opening the bottle.Cor e Forma:LiquidReagecon Ammonia (Ammonium Hydroxide) TS Solution according to United States Pharmacopoeia (USP)
CAS:Reagecon's Ammonia (Ammonium Hydroxide) TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Diluted Alcohol (50/50 Alcohol Water) Solution according to United States Pharmacopoeia (USP)
Reagecon's Diluted Alcohol (50/50 Alcohol Water) Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Ferric Chloride TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Ferric Chloride TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Phenolphthalein TS/RS Solution according to United States Pharmacopoeia (USP)
Reagecon's Phenolphthalein TS/RS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Edetate Disodium 0.05M according to United States Pharmacopoeia (USP)
Reagecon's Edetate Disodium 0.05M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Sodium Acetate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Sodium Acetate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Mercuric Chloride TS Solution according to United States Pharmacopoeia (USP)
CAS:Reagecon's Mercuric Chloride TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon pH 7.41 at 25°C according to United States Reagecon pHarmacopoeia (USP)
Reagecon's pH 7.41 at 25°C according to United States Reagecon's pHarmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Cupric Acetate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Cupric Acetate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon pH 4.01 at 25°C Potassium Bi Phthalate 0.05M according to United States Pharmacopoeia (USP)
Reagecon's pH 4.01 at 25°C Potassium Bi Phthalate 0.05M according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Phosphotungstic Acid TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Phosphotungstic Acid TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Calcium Sulfate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Calcium Sulfate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Silver Nitrate 0.05N according to United States Pharmacopoeia (USP)
Reagecon's Silver Nitrate 0.05N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon pH 3.56 at 25°C Potassium Hydrogen Tartrate Saturated according to United States Pharmacopoeia (USP)
Reagecon's pH 3.56 at 25°C Potassium Hydrogen Tartrate Saturated according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Sodium Hydroxide Alcoholic 0.1N according to United States Pharmacopoeia (USP)
Reagecon's Sodium Hydroxide Alcoholic 0.1N according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Ammonium Ferric Sulfate 8% Solution in Water according to United States Pharmacopoeia (USP)
Reagecon's Ammonium Ferric Sulfate 8% according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. Has guaranteed stability throughout its entire shelf life, even after opening the bottle.Cor e Forma:LiquidReagecon Ammonium Thiocyanate 0.1N according to United States Pharmacopoeia (USP)
Reagecon's Ammonium Thiocyanate 0.1N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon pH 6.50 Monobasic Potassium Phosphate Buffered Eluent in accordance with United States Pharmacopoeia (USP)
Reagecon's pH 6.5 Monobasic Potassium Phosphate Buffered Eluent is tested, is NIST traceable and has guaranteed stability throughout its entire shelf life, even after opening the bottle. The product is developed, formulated and specified in accordance with United States Pharmacopoeia (USP) requirements.Cor e Forma:LiquidReagecon Mercuric Chloride TS Solution according to United States Pharmacopoeia (USP)
CAS:Reagecon's Mercuric Chloride TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Ferric Ammonium Sulfate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Ferric Ammonium Sulfate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon pH 9.18 at 25°C Sodium Tetraborate 0.01M according to United States Pharmacopoeia (USP)
Reagecon's pH 9.18 at 25°C Sodium Tetraborate 0.01M according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Potassium Bromate 0.1N according to United States Pharmacopoeia (USP)
Reagecon's Potassium Bromate 0.1N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon AVL is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stoichiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Cupric Sulfate TS Solution according to United States Pharmacopoeia (USP)
CAS:Reagecon's Cupric Sulfate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Hydrochloric Acid 0.5N according to United States Pharmacopoeia (USP)
Reagecon's Hydrochloric Acid 0.5N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Potassium Dichromate 0.1N according to United States Pharmacopoeia (USP)
Reagecon's Potassium Dichromate 0.1N is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon pH 1.68 at 25°C Potassium Tetroxalate 0.05M according to United States Pharmacopoeia (USP)
Reagecon's pH 1.68 at 25°C Potassium Tetroxalate 0.05M according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Methyl Orange Indicator conforms to United States Pharmacopoeia (USP)
Reagecon's Methyl Orange Indicator Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator, titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's’s facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Cor e Forma:LiquidReagecon Calcium Sulfate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Calcium Sulfate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Potassium Iodide TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Potassium Iodide TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon pH 12.45 at 25°C Calcium Hydroxide Saturated according to United States Pharmacopoeia (USP)
Reagecon's pH 12.45 at 25°C Calcium Hydroxide Saturated according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Sodium Chloride Solution according to United States Pharmacopoeia (USP)
Reagecon's Sodium Chloride Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Edetate Disodium 0.1M according to United States Pharmacopoeia (USP)
Reagecon's Edetate Disodium 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Potassium Carbonate TS Solution according to United States Pharmacopoeia (USP)
Reagecon's Potassium Carbonate TS Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Cupric Tartrate Alkaline (Fehling's) Solution conforms to United States Pharmacopoeia (USP)
Reagecon's Cupric Tartrate Alkaline (Fehling's) Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator, titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's’s facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry. Supplied as 1x500ml Fehlings Solution No. 1 and 1x500ml Fehlings Solution No. 2.Cor e Forma:LiquidReagecon Sodium Chloride Solution according to United States Pharmacopoeia (USP)
Reagecon's Sodium Chloride Solution according to United States Pharmacopoeia (USP) is specified for use in individual United States Pharmacopoeia (USP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03); is NIST traceable and has guaranteed stability throughout its entire shelf life; even after opening the bottle.Cor e Forma:LiquidReagecon Bismuth Nitrate 0.01M according to United States Pharmacopoeia (USP)
Reagecon's Bismuth Nitrate 0.01M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several USP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidDiethylene glycol monoethyl ether, Ph. Eur., USP grade
CAS:Fórmula:C6H14O3Pureza:≥ 99.900%Cor e Forma:Colourless liquidPeso molecular:134.18Crystal Violet (C.I. 42555); USP grade
CAS:Fórmula:C25H30ClN3Pureza:≤ 1.0%Cor e Forma:Green to dark green crystalline powderPeso molecular:407.99Methotrexate EP Impurity E-13C-d3 (Methotrexate USP Related Compound E-13C-d3)
Fórmula:C1413CH12D3N7O2Peso molecular:329.34Sodium gluconate, USP grade
CAS:Fórmula:C6H11NaO7Pureza:98.0 - 102.0 %Cor e Forma:White or almost white crystalline powderPeso molecular:218.13Leflunomide
CAS:Fórmula:C12H9F3N2O2Pureza:≥ 98.0%Cor e Forma:White to off-white powderPeso molecular:270.21N-Nitroso Lacosamide EP Impurity D (N-Nitroso Lacosamide USP Related Compound D (Free Form))
Fórmula:C11H15N3O3Peso molecular:237.26Rotigotine EP Impurity G (Rotigotine USP Related Compound G (Free Form))
CAS:Fórmula:C22H25NOS2Peso molecular:383.57ent-Acetylcysteine EP Impurity C (ent-Acetylcysteine USP Related Compound C)
CAS:Fórmula:C10H16N2O6S2Peso molecular:324.37Methotrexate EP Impurity B (Methotrexate USP Related Compound B)
CAS:Fórmula:C19H20N8O5Peso molecular:440.42N-Nitroso Trospium Chloride EP Impurity B (N-Nitroso Trospium Chloride USP Related Compound B)
Fórmula:C21H22N2O4Peso molecular:366.42Methotrexate EP Impurity E (Methotrexate USP Related Compound E (Free Form))
CAS:Fórmula:C15H15N7O2Peso molecular:325.33Terbinafine EP Impurity A-13C-d3 ( Terbinafine USP Related Compound A-13C-d3 (Free Form))
Fórmula:C1113CH10D3NPeso molecular:175.25Rac-Levodopa EP Impurity A HCl (Rac-Levodopa USP Related Compound A HCl, 6-Hydroxy DOPA HCl)
CAS:Fórmula:C9H11NO5·HClCor e Forma:Dark Brown SolidPeso molecular:213.19 36.46N-Nitroso Dipyridamole EP Impurity F (N-Nitroso Dipyridamole USP Related Compound F)
Fórmula:C21H35N9O6Peso molecular:509.57Bicalutamide Sulfoxide (Bicalutamide USP Related Compound A)
CAS:Fórmula:C18H14F4N2O3SCor e Forma:White To Off-White SolidPeso molecular:414.38Granisetron EP Impurity E (Granisetron USP Related Compound E (Free Form))
CAS:Fórmula:C9H18N2Peso molecular:154.26Cilostazol USP Related Compound B-d11 (Cilostazol Metabolite (OPC-13015)-d11)
CAS:Fórmula:C20H14D11N5O2Peso molecular:378.52Iminostilbene-d2 (Carbamazepine EP Impurity D-d2, Carbamazepine USP Related Compound B-d2, Dibenzazepine-d2)
CAS:Fórmula:C14H9D2NPeso molecular:195.26Irbesartan
CAS:Fórmula:C25H28N6OPureza:98.0 - 102.0 % (dry basis)Cor e Forma:White to off-white powderPeso molecular:428.53Desogestrel EP Impurity C-d2 (Desogestrel USP Related Compound D-d2)
CAS:Fórmula:C20H26D2OPeso molecular:286.46Disodium hydrogen phosphate heptahydrate, USP grade
CAS:Fórmula:Na2HPO4·7H2OPureza:98.0 - 100.5 % (dried basis)Cor e Forma:White crystals or crystalline powderPeso molecular:268.07Alclometasone dipropionate
CAS:Fórmula:C28H37ClO7Pureza:97.0 - 102.0 %Cor e Forma:White to off-white crystalline powderPeso molecular:521.04Chloramphenicol, USP grade
CAS:Fórmula:C11H12Cl2N2O5Pureza:97.0 - 103.0 %Cor e Forma:White to light-yellow crystalline powderPeso molecular:323.14Clomifene (Clomiphene) EP Impurity A HCl (Clomiphene USP Related Compound A)
CAS:Fórmula:C26H29NO·HClPeso molecular:371.52 36.46Fosinopril EP Impurity C (Fosinopril USP Related Compound C)
Fórmula:C30H45NO7P·NaPeso molecular:562.67 22.99N-Nitroso Lansoprazole EP Impurity C (N-Nitroso Lansoprazole USP Related Compound B (Free Form), N-Nitroso Lansoprazole Sulfide)
CAS:Fórmula:C16H13F3N4O2SPeso molecular:382.36N-Nitroso Nicardipine EP Impurity C (N-Nitroso Nicardipine USP Related Compound C, N-Nitroso Nitrendipine EP Impurity B)
Fórmula:C17H17N3O7Peso molecular:375.34N-Nitroso Timolol EP Impurity E (N-Nitroso Timolol USP Related Compound E (Free Form))
Fórmula:C17H25N5O7SPeso molecular:443.48D-(-)-Fructose
CAS:Fórmula:C6H12O6Pureza:92.0 - 102.0 % (dried basis)Cor e Forma:White, hygroscopic, crystalline powderPeso molecular:180.16(S)-Selegiline EP Impurity D ((S)-Selegiline USP Related Compound D (Free Form), (S)-N-Desmethyl Selegiline)
Fórmula:C12H15NPeso molecular:173.40Clonidine EP Impurity B-d4 (Clonidine USP Related Compound A-d4)
Fórmula:C11H7D4Cl2N3OPeso molecular:276.15Tryptophan USP Related Compound B (N-Acetyl-L-Tryptophan)
CAS:Fórmula:C13H14N2O3Peso molecular:246.27Doxepin EP Impurity C-13C-d3 HCl ((E)-Doxepin USP Related Compound C-13C-d3, Desmethyl (E)-Doxepin-13C-d3 HCl, (E)-Nordoxepin-13C-d3 HCl)
CAS:Fórmula:C1713CH16D3NO·HClPeso molecular:269.37 36.46Ketamine EP Impurity A (Z-isomer) HCl (Ketamine USP Related Compound A (Z-isomer HCl )
CAS:Fórmula:C13H16ClNO·HClPeso molecular:237.73 36.46Metoprolol EP Impurity O-d7 HCl (Metoprolol USP Related Compound D-d7) (Mixture of Diastereomers)
CAS:Fórmula:C27H34D7NO6·HClPeso molecular:482.67 36.46Pamabrom USP Related Compound A-d6 (8-Chlorotheophylline-d6)
CAS:Fórmula:C7HD6ClN4O2Peso molecular:220.65N-Nitroso Tropicamide EP Impurity A (N-Nitroso Tropicamide USP Related Compound A)
CAS:Fórmula:C8H11N3OPeso molecular:165.20Sevoflurane EP Impurity B (Sevoflurane USP Related Compound B)
CAS:Fórmula:C4H4F6OPeso molecular:182.07Buspirone EP Impurity L (Buspirone USP Related Compound L)
CAS:Fórmula:C13H20ClNO2Peso molecular:257.76Magnesium gluconate, USP grade
CAS:Fórmula:C12H22MgO14·xH2OPureza:98.0 - 102.0 % (anhydrous basis)Cor e Forma:White to off-white powderPeso molecular:414.60 (anhydrous)Melphalan, USP grade
CAS:Fórmula:C13H18Cl2N2O2Pureza:94.0 - 100.5 % (dried, ionisable chlorine-free basis)Cor e Forma:White to almost white powderPeso molecular:305.20Ziprasidone EP Impurity D (Ziprasidone USP Related Compound C)
CAS:Fórmula:C42H40Cl2N8O3S2Peso molecular:839.87Metoprolol EP Impurity O-d7 (Metoprolol USP Related Compound D-d7 (Free Form)) (Mixture of Diastereomers)
CAS:Fórmula:C27H34D7NO6Peso molecular:482.67Omeprazole EP Impurity C-d3 (Omeprazole USP Related Compound C-d3, Esomeprazole EP Impurity C-d3) (on benzene)
CAS:Fórmula:C17H16D3N3O2SPeso molecular:332.44Iron(II) gluconate dihydrate, USP grade
CAS:Fórmula:C12H22FeO14·2H2OPureza:97.0 - 102.0 %Cor e Forma:Light yellow to light green powderPeso molecular:482.19Orlistat USP Related Compound B (Diisopropyl Hydrazine-1, 2-Dicarboxylate)
CAS:Fórmula:C8H16N2O4Peso molecular:204.23DL-α-Tocopherol, Ph. Eur., USP grade
CAS:Fórmula:C29H50O2Pureza:96.0 - 102.0 % (USP)Cor e Forma:Pale yellow to brown, clear viscous liquidPeso molecular:430.72N-Nitroso Isoprenaline HCl EP Impurity A (N-Nitroso Isoproterenol USP Related Compound A)
Fórmula:C11H14N2O4Peso molecular:238.24Procainamide hydrochloride
CAS:Fórmula:C13H21N3O·HClPureza:≥ 98.0% (dried basis)Cor e Forma:White to off-white powderPeso molecular:271.79N-Nitroso Chlorcyclizine EP Impurity A-d11 (N-Nitroso Cyclizine EP Impurity A-d11, N-Nitroso Cyclizine USP Related Compound A-d11)
CAS:Fórmula:C5D11N3OPeso molecular:140.23Famotidine EP Impurity B (Famotidine USP Related Compound B)
CAS:Fórmula:C16H23N11O2S5Peso molecular:561.75Dimethyl sulfoxide, Ph. Eur., USP grade
CAS:Fórmula:(CH3)2SOPureza:≥ 99.9%Cor e Forma:Colourless liquid, crystals or solidPeso molecular:78.13Anatabine (Nicotine EP Impurity A, (S)-Nicotine USP Related Compound A)
CAS:Fórmula:C10H12N2Peso molecular:160.22Sevoflurane EP Impurity C (Sevoflurane USP Related Compound C)
CAS:Fórmula:C3H2F6OPeso molecular:168.04Latanoprost EP Impurity H-d4 (Latanoprost USP Related Compound E-d4)
CAS:Fórmula:C23H30D4O5Peso molecular:394.54Pantoprazole EP Impurity B-d6 (Pantoprazole USP Related Compound B-d6, Pantoprazole Sulfide-d6)
CAS:Fórmula:C16H9D6F2N3O3SPeso molecular:373.41N-Nitroso Tetracaine EP Impurity B-d9 (N-Nitroso Tetracaine USP Related Compound B-d9
Fórmula:C11H5D9N2O3Peso molecular:231.299Perindopril EP Impurity F-d4 (Perindopril USP Related Compound F-d4)
CAS:Fórmula:C19H26D4N2O4Peso molecular:354.48Diphenhydramine hydrochloride
CAS:Fórmula:C17H21NO·HClPureza:≥ 98.0%Cor e Forma:White powderPeso molecular:291.82N-Nitroso Selegiline EP Impurity D (N-Nitroso Selegiline USP Related Compound D (Free Form), N-Nitroso-N-Desmethyl Selegiline)
Fórmula:C12H14N2OPeso molecular:202.26Cefepime EP Impurity E (Cefepime USP Related Compound E (Free Form))
CAS:Fórmula:C13H19N3O3SPeso molecular:297.38Salbutamol EP Impurity I (R-isomer) (Levalbuterol USP Related Compound F)
CAS:Fórmula:C20H27NO3Peso molecular:329.44Chlorcyclizine EP Impurity A-d11 (Cyclizine EP Impurity A-d11, Cyclizine USP Related Compound A-d11)
CAS:Fórmula:C5HD11N2Peso molecular:111.23Omeprazole EP Impurity I-d3 (Omeprazole USP Related Compound I-d3, Omeprazole Sulfone N-Oxide-d3) (on pyridine)
Fórmula:C17H16D3N3O5Peso molecular:380.43Lansoprazole EP Impurity C-d4 (Lansoprazole USP Related Compound B-d4 (Free Form), Lansoprazole Sulfide-d4)
CAS:Fórmula:C16H10D4F3N3OSPeso molecular:357.39Lansoprazole EP Impurity B N-Oxide-d4 (Lansoprazole USP Related Compound A N-Oxide-d4, Lansoprazole Sulfone N-Oxide-d4)
CAS:Fórmula:C16H10D4F3N3O4SPeso molecular:405.38Zolmitriptan EP Impurity G-13C-d3 (Zolmitriptan USP Related Compound A-13C-d3, N-Desmethyl Zolmitriptan-13C-d3)
CAS:Fórmula:C1413CH16D3N3O2Peso molecular:277.35Lactose, anhydrous, Ph. Eur., USP grade
CAS:Fórmula:C12H22O11Pureza:≥ 99.5% (alpha + beta)Cor e Forma:White or almost white crystalline powderPeso molecular:342.30N-Nitroso Timolol EP Impurity B (N-Nitroso Timolol USP Related Compound B)
Fórmula:C13H23N5O4SPeso molecular:345.42N-Nitroso Lacosamide EP Impurity D (R-Isomer) (N-Nitroso Lacosamide USP Related Compound D (R-Isomer) (Free Form))
Fórmula:C11H15N3O3Peso molecular:237.26N1-Nitroso Lacosamide EP Impurity B (R-Isomer) (N1-Nitroso Lacosamide USP Related Compound B (R-Isomer), N1-Nitroso O-Acetyl Lacosamide)
Fórmula:C14H17N3O5Peso molecular:307.31Iopamidol EP Impurity H (Iopamidol USP Related Compound C)
Fórmula:C17H22ClI2N3O8Peso molecular:685.63N1-Nitroso Lacosamide EP Impurity F (R-Isomer) (N1-Nitroso Lacosamide USP Related Compound F (R-Isomer))
Fórmula:C12H15N3O4Peso molecular:265.27N1-Nitroso Lacosamide EP Impurity F (S-Isomer) (N1-Nitroso Lacosamide USP Related Compound F (S-Isomer))
Fórmula:C12H15N3O4Peso molecular:265.27N-Nitroso Torasemide (Torsemide) EP Impurity C (N-Nitroso Torasemide (Torsemide) USP Related Compound C)
Fórmula:C15H17N5O4SPeso molecular:363.39N2-Nitroso Cyclophosphamide EP Impurity E (N2-Nitroso Cyclophosphamide USP Related Compound D)
Fórmula:C7H17ClN3O5PPeso molecular:289.65Di-N-Nitroso Cyclophosphamide EP Impurity E (Di-N-Nitroso Cyclophosphamide USP Related Compound D)
Fórmula:C7H16ClN4O6PPeso molecular:318.65di-Sodium hydrogen phosphate dodecahydrate, 99%, Ph. Eur., USP grade
CAS:Fórmula:Na2HPO4·12H2OPureza:98.5 - 102.5 % (Ph. Eur. test)Cor e Forma:Colourless crystals or white crystalline powderPeso molecular:358.14Tetracycline hydrochloride, USP grade
CAS:Fórmula:C22H24N2O8·HClCor e Forma:Yellow powderPeso molecular:480.91N-Nitroso Lidocaine EP Impurity H (N-Nitroso Lidocaine USP Related Compound H)
Fórmula:C10H11ClN2O2Peso molecular:226.66Albendazole EP Impurity D-d7 (Albendazole USP Related Compound D-d7)
Fórmula:C10H6D7N3O2SPeso molecular:246.34N-Nitroso rac-Anatabine-d4 (N-Nitroso rac-Nicotine EP Impurity A-d4, N-Nitroso Nicotine USP Related Compound A-d4)
CAS:Fórmula:C10H7D4N3OPeso molecular:193.24Orlistat USP Related Compound C
CAS:Fórmula:C18H15OPCor e Forma:White To Off-White SolidPeso molecular:278.29N-Nitroso Terbinafine EP Impurity A-13C-d3 (N-(Nitroso Terbinafine USP Related Compound A-13C-d3 (Free Form))
Fórmula:C1113CH9D3N2OPeso molecular:204.25N-Nitroso Ticagrelor EP Impurity B (N-Nitroso Ticagrelor USP Related Compound B)
Fórmula:C23H27F2N7O5SPeso molecular:551.57(R)-Irinotecan EP Impurity E ((R)-Irinotecan USP Related Compound B, (R)-7-Ethyl-10-Hydroxy Camptothecin)
CAS:Fórmula:C22H20N2O5Peso molecular:392.42Insulin Human, recombinant
CAS:Fórmula:C257H383N65O77S6Pureza:95.0 - 105.0 % (dried basis)Cor e Forma:White to off-white powderPeso molecular:5807.57Irinotecan EP Impurity E-d3 (Irinotecan USP Related Compound B-d3, (S)-7-Ethyl-10-Hydroxy Camptothecin-d3)
Fórmula:C22H17D3N2O5Peso molecular:395.45Clobazam USP Related Compound G HCl
Fórmula:C15H14ClN2·Cl·HClCor e Forma:Off-White SolidPeso molecular:257.74 35.45 36.46Ursodiol USP Related Compound H-d5 (Ursodeoxycholic Acid EP Impurity H-d5 , Isoursodeoxycholic Acid-d5)
Fórmula:C24H35D5O4Peso molecular:397.61Ciclopirox EP Impurity B (Ciclopirox USP Related Compound B)
CAS:Fórmula:C12H16O2Peso molecular:192.26Doxepin EP Impurity C-d3 HCl ((E)-Doxepin USP Related Compound C-d3, Desmethyl (E)-Doxepin-d3 HCl, (E)-Nordoxepin-d3 HCl)
Fórmula:C18H16D3NO·HClPeso molecular:268.38 36.46Almotriptan EP Impurity D (Almotriptan USP Related Compound B)
CAS:Fórmula:C15H21N3O2SC4H4O4Peso molecular:307.41 1/2*116.07rac-Irinotecan EP Impurity E (rac-Irinotecan USP Related Compound B, rac-7-Ethyl-10-Hydroxy Camptothecin)
Fórmula:C22H20N2O5Peso molecular:392.42Rabeprazole EP Impurity A-d3 (Rabeprazole USP Related Compound D-d3, Rabeprazole Sulfone-d3)
CAS:Fórmula:C18H18D3N3O4SPeso molecular:378.46N-Nitroso Tetracaine EP Impurity C (N-Nitroso Tetracaine USP Related Compound C)
Fórmula:C12H16N2O3Peso molecular:236.27



