Étalons physico-chimiques

Reagecon's Potassium Hydroxide Alcoholic 0.1M 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.

Reagecon's DIN 19267 pH Buffer Solution at 25°C is tested by our ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable.

Reagecon's Potassium Dichromate 0.167M (1.0N) Analytical Volumetric Solution (AVL) is a fully factorised, high purity, stable product, developed and tested for oxidation/reduction titrations.  This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.1%. 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.  Oxidation/reduction titrations depend on changes in the electropotential of the oxidation reduction system and always involves a reaction between an oxidising and reducing pair. - 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 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.

Reagecon's DIN 19266 pH Buffer Solution at 25°C is tested by our ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable.

Pricing displayed is Nett. For order quantities above 4 units, ask your sales contact for a quotation. Reagecon's Multi Element Standard for ICP; ICP-MS in 2-5% Nitric Acid (HNO₃) is manufactured from ultra-pure metals or salts. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density. The results are reported in mg/kg and mg/L on the basis of weight and density. Reagecon hold ISO 17025 (A2LA Ref: 6739.02) accreditation for calibration of laboratory balances. - GHS/OSHA compliant, REACH - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards), triple distilled acids and triple leached pre-cleaned bottles. The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards, where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level. Description | Concentration: - Aluminium (Al): 500 µg/mL (ppm). - Barium (Ba): 500 µg/mL (ppm). - Boron (B): 500 µg/mL (ppm). - Calcium (Ca): 500 µg/mL (ppm). - Chromium (Cr): 500 µg/mL (ppm). - Copper (Cu): 500 µg/mL (ppm). - Iron (Fe): 500 µg/mL (ppm). - Lead (Pb): 500 µg/mL (ppm). - Magnesium (Mg): 500 µg/mL (ppm). - Manganese (Mn): 500 µg/mL (ppm). - Molybdenum (Mo): 500 µg/mL (ppm). - Nickel (Ni): 500 µg/mL (ppm). - Phosphorus (P): 500 µg/mL (ppm). - Potassium (K): 500 µg/mL (ppm). - Silicon (Si): 500 µg/mL (ppm). - Silver (Ag): 500 µg/mL (ppm). - Sodium (Na): 500 µg/mL (ppm). - Zinc (Zn): 500 µg/mL (ppm).

The use of Reagecon's Fluoride TISAB 3 Ionic Strength Adjuster (ISA) is necessary as an additive when using an Ion Selective Electrode (ISE) for the measurement of Fluoride. The ISA is added to both the Ion Selective Electrode Calibration Solution (ISE) and the sample; so as to keep the ionic strength of both standard and test high; eliminate matrix effects and suppress or eliminate interfering ions. - For use as an Ionic Strength Adjuster (ISA) when performing Fluoride TISAB 3 measurement by Ion Selective Electrode (ISE) - Suppresses interfering ions; eliminates matrix; hysteresis and liquid junction potentials. - Eliminates or reduces error due to temperature co-efficient of variation between sample and calibration standard. - High ionic strength. - Aqueous matrix. - Manufactured to exacting specifications with an extended shelf life and stability; even after opening the bottle.

Reagecon Nitric Acid Dilute is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications.  These include the preparation of other reagents (4.1.1), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.

Reagecon’s Technical pH Buffer Solution at 25°C is colour coded for ease of use. Tested by our ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable.

Reagecon's Yttrium Standard for ICP; ICP-MS 1000 µg/mL (1000 ppm) in 2-5% Nitric Acid (HNO₃) for ICP or ICP-MS is manufactured from ultra-pure metal (99.999%). This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density. To a specification of ± 0.2%. The results are reported in mg/kg and mg/L on the basis of weight and density. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - GHS/OSHA compliant, REACH - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards), triple distilled acids and triple leached pre-cleaned bottles. The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards, where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.

Reagecon's Simulated Gastric Fluid without Enzyme Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 384ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 384ml of solution, each 384ml bottle is diluted to give 10L of ready to use Dissolution Medium.

Reagecon's Phosphate Standard for Ion Chromatography (IC) 0.01 mg/mL (10 ppm) in H₂O is manufactured from ultra-pure material. This product is manufactured gravimetrically. Prior to bottling; the final product is tested and verified using a state of the art ion chromatograph and is reported using the gravimetric result; corrected for density; to a specification of ± 0.2%. The results are reported in mg/kg and mg/L on the basis of weight and density. Reagecon holds ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - GHS/OSHA compliant, REACH - This product is produced in a highly controlled cleanroom (ISO 7) environment; using ultra-pure water (specially treated for the production of ion chromatography standards) and triple leached pre-cleaned bottles. All of the uncertainties of measurement for the product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.

Reagecon's Spectrophotometry Stray Light Inorganic 227nm Cut-off Filter - Lithium Carbonate is formulated to give zero absorbance at 227 nm wavelength. This standard is used to indicate to the analyst that the instrument is measuring light omitted from a source, other than through the sample cuvette.

This Reagecon's 200 mV (± 5mV) Standard acts as a Control or Reference Material. This is because Redox Oxidation/Reduction (ORP) is an absolute measurement and the sensing electrode does not require calibration. This Standard verifies the functionality of the sensing and reference electrode; the analysts technique; environmental conditions and the operation of the measuring meter. The value of 200 mV quoted refers to the potentials of the platinum electrode v Ag/AgCl reference electrode. - Reagecon produces a complete range of high-quality Redox Standards for the control; validation or qualification of Redox measurement. - Very high specification (± 5mV). - Manufactured to exacting specifications with an extended shelf life and stability; even after opening the bottle. - All products are tested with proven verifiable accuracy and fully budgeted uncertainty of measurement.

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.

Reagecon's Spectrophotometry Holmium Oxide Solution UV and Visible Wavelength Standard a standard which gives peak wavelengths between 240 nm and 640 nm that includes a spectral scan at various wavelengths including 0.1, 0.2, 0.5, 1.0 and 2.0 nm slit widths. Therefore, this standard is used for validation of the wavelength scale of a spectrophotometer in both the UV and Visible regions.

Reagecon's Lanthanum Standard for ICP; ICP-MS 1000 µg/mL (1000 ppm) in 2-5% Nitric Acid (HNO₃) for ICP or ICP-MS is manufactured from ultra-pure metal (99.999%). This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density. To a specification of ± 0.2%. The results are reported in mg/kg and mg/L on the basis of weight and density. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - GHS/OSHA compliant, REACH - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards), triple distilled acids and triple leached pre-cleaned bottles. The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards, where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.

Reagecon's Simulated Intestinal Fluid w/o Enzyme Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 230.85ml in volume in each bottle and the contents of each bottle can be diluted to produce 6L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 230.85ml of solution, each 230.85ml bottle is diluted to give 6L of ready to use Dissolution Medium.

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.

Reagecon's Sulphuric Acid 0.1M (0.2N) Analytical Volumetric Solution (AVL) is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03). This product is a fully factorised; high purity; stable product; developed and tested for acid/base titrations. This Analytical Volumetric Solution; also called titrant; standard titrant or standard solution; is tested to a specification of ± 0.1%. 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. Acid/base titrations; also called neutralisation titrations; are used to determine either the amount of acid/base in a sample or the substance that can be converted to an acid/base. - 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 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.

Reagecon's Refractive Index Standards (Stabilised Sucrose) 1.44193 nD at 20°C is a high quality product, with an extended shelf life to be used either as a calibrant or analytical control material for use in Refractive Index based methods for Refractive Index determination. This product can be used on any make or model of refractometer. The product is tested using a state of the art refractometer, manufactured gravimetrically and is traceable. Reagecon holds ISO 17025 accreditation for the test method used to certify this product. - Reagecon holds ISO 17025 accreditation (A2LA Ref: 6739.03) for testing Refractive Index (Brix standards) using refractometry. This product has an uncertainty of measurement of ± 0.00014 nD units. It is stable for one year; either opened or unopened and is presented in a convenient 15ml dropper bottle. The product is prepared gravimetrically on a weight/weight basis. Both solute and solvent are weighed on a balance calibrated by OIML traceable weights. Reagecon holds ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - High accuracy (± 0.00014 nD units) - Tested using a state of the art Refractometer