
Building Blocks de hidrocarburos
Los building blocks hidrocarbonados son compuestos orgánicos formados únicamente por átomos de carbono e hidrógeno. Estas estructuras fundamentales sirven como base para la síntesis de una amplia variedad de moléculas complejas. Los building blocks hidrocarbonados se utilizan en el desarrollo de productos farmacéuticos, polímeros y otros compuestos orgánicos. En CymitQuimica, ofrecemos una amplia gama de building blocks hidrocarbonados de alta calidad para facilitar tus proyectos de síntesis e investigación.
Subcategorías de "Building Blocks de hidrocarburos"
Se han encontrado 5575 productos de "Building Blocks de hidrocarburos"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Docosane
CAS:<p>Please enquire for more information about Docosane including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Fórmula:C22H46Pureza:Min. 95%Peso molecular:310.6 g/mol2-Bromo-2-nitro-1,3-propanediol
CAS:<p>2-Bromo-2-nitro-1,3-propanediol (BNP) is a preservative that is used in wastewater treatment. It is an antimicrobial agent that has synergistic effects with other antimicrobial agents such as triclosan, benzalkonium chloride and sesquiterpene lactones. 2-Bromo-2-nitro-1,3-propanediol has been shown to have a phase transition temperature of -28°C, which can be used to identify it in the laboratory. This compound also has a pK value of 4.4, which indicates that it is weakly acidic. 2-Bromo-2-nitro-1,3-propanediol can be used as an analytical method for the determination of p - hydroxybenzoic acid in aqueous samples by electrochemical impedance spectroscopy (EIS).</p>Fórmula:C3H6BrNO4Pureza:Min. 95%Forma y color:PowderPeso molecular:199.99 g/mol2-(2-Phenoxyethoxy)ethanol
CAS:<p>2-(2-Phenoxyethoxy)ethanol is a fine chemical and a useful building block. It is an important intermediate in the synthesis of other chemicals, such as pharmaceuticals, herbicides, and pesticides. 2-(2-Phenoxyethoxy)ethanol can be used as a research chemical or reagent. It can also be used to prepare complex compounds and versatile scaffolds. CAS No. 104-68-7</p>Fórmula:C10H14O3Pureza:Min. 95.0 Area-%Peso molecular:182.24 g/molHexabromoethane
CAS:<p>Hexabromoethane is a metal chelate that has been shown to activate the polymerization of cyclohexane rings. It is often used as a light-sensitive initiator for the production of polymers, such as polyethylene. Hexabromoethane can also be found in some halogenated compounds and hydroxyl groups. The molecule is made up of six bromine atoms, an ethane chain, and one hydrogen atom. Hexabromoethane has significant interactions with other functional groups, including hydroxyls and monomers.</p>Fórmula:C2Br6Pureza:Min. 95%Forma y color:PowderPeso molecular:503.45 g/molChlorobutanol
CAS:<p>Chlorobutanol is an antimicrobial agent that is used in the preservation of pharmaceuticals, cosmetics, and other products. It has been shown to be effective against a variety of bacterial and fungal organisms. Chlorobutanol is also used as a preservative in topical ophthalmic preparations. In addition, chlorobutanol has been found to be a potent inhibitor of histone deacetylase (HDAC) activity, which may be due to its ability to bind to the active site of HDACs. This binding prevents acetylation of lysine residues on histones, thereby preventing transcriptional activation.</p>Fórmula:C4H7OCl3Pureza:Min. 95%Forma y color:White To Off-White SolidPeso molecular:177.46 g/mol2-Nitropropane
CAS:<p>2-Nitropropane is a pharmacological agent that is used for the treatment of bacterial infections. It is a nitroalkane, which are compounds with nitro groups in their molecular structure. 2-Nitropropane has been shown to inhibit DNA synthesis by binding to nuclear dna and inhibiting enzyme activities in vitro. Toxicological studies on 2-nitropropane have been conducted and show that it does not cause any adverse effects at low doses. The mechanism of action for 2-nitropropane has been investigated and found to inhibit the enzyme activity of nitrate reductase, which leads to an accumulation of the toxic nitrite ion (NO2-) in cells.</p>Fórmula:C3H7NO2Pureza:Min. 95%Forma y color:Colorless PowderPeso molecular:89.09 g/molHydroxypropanedial
CAS:<p>Hydroxypropanedial is a hydroxy group-containing compound that is not found in natural sources. It has antioxidative properties, which may be due to its ability to scavenge reactive oxygen species or donate hydrogen atoms to free radicals. The compound also has cyclohexane ring and carbonyl groups, which are responsible for the hydroxyl and carboxylic acid functionalities respectively. This substance is used as a chromatographic reagent to measure second-order rate constants of reactions involving hydroxyl radicals. Hydroxypropanedial absorbs light strongly at wavelengths shorter than 300 nm, which is the most effective wavelength range for uv absorption in biological systems.</p>Fórmula:C3H4O3Pureza:Min. 95%Forma y color:Off-White To Light (Or Pale) Brown SolidPeso molecular:88.06 g/mol1-Amino-1-cyclopentanecarboxamide
CAS:<p>1-Amino-1-cyclopentanecarboxamide is a bicyclic heterocycle that has been shown to have therapeutic effects in the treatment of autoimmune diseases and cancer. It is structurally related to chemokines, which are cytokines that induce inflammatory responses by activating the immune system. 1-Amino-1-cyclopentanecarboxamide binds to specific receptors on white blood cells, resulting in an increase in the production of chemokines and other proinflammatory molecules. This leads to an increase in inflammation, as well as an increase in blood pressure. The chemical also has anti-inflammatory properties and can be used for the treatment of inflammatory diseases such as arthritis. 1-Amino-1-cyclopentanecarboxamide has been shown to inhibit cancer cell growth by inducing apoptosis (programmed cell death).</p>Fórmula:C6H12N2OPureza:Min. 95%Forma y color:PowderPeso molecular:128.17 g/molPerfluoroheptanoyl chloride
CAS:<p>Perfluoroheptanoyl chloride is a fluorinated hydrocarbon that is used as a surfactant in detergent compositions. It has been shown to be biostable, which means it does not react with other molecules in the environment. This compound also has low environmental toxicity because of its resistance to peroxidation and its ability to form stable complexes with metals. Perfluoroheptanoyl chloride has been shown to cause allergic reactions in some people and may cause adverse effects on animal health. Research on the effects of perfluoroheptanoyl chloride on Xenopus oocytes has demonstrated that this compound can affect gene expression and result in cell death.</p>Fórmula:C7CIF13OPureza:Min. 95%Forma y color:Colourless LiquidPeso molecular:382.51 g/mol1,2-Ethanedithiol
CAS:<p>1,2-Ethanedithiol is a molecule that consists of a sulfur atom and two ethyl groups. It can form stable complexes with hydrogen fluoride and trifluoroacetic acid as well as hydrochloric acid. 1,2-Ethanedithiol is reactive with nucleophiles such as amines, thiols, and alcohols. The molecule has an electrochemical impedance spectroscopy (EIS) model system that has shown to react with the electron flow from the electrode to the solution of a compound. The EIS model system also showed that a conformational change in the molecule could result in light emission.</p>Fórmula:C2H6S2Pureza:Min. 95%Forma y color:Colorless Clear LiquidPeso molecular:94.2 g/molEthanesulfonic acid, 70% aqueous solution
CAS:<p>Ethanesulfonic acid solution - 70 wt. % in H2O is a monosodium salt that is used as an enzymatic reagent for the determination of bacteria and fungi, as well as for the detection of infectious diseases. It has been shown to be effective against microdialysis probes with a high degree of sensitivity and specificity. Ethanesulfonic acid solution - 70 wt. % in H2O has been shown to have significant physiological effects on various regions of the body, including bowel disease, polymerase chain reaction (PCR), glycol ethers, antimicrobial agents, and radiation. Ethanesulfonic acid solution - 70 wt. % in H2O also inhibits the growth of bacteria by acting as a coumarin derivative that reacts with nucleotides to form dinucleotide phosphate, which blocks DNA synthesis and transcription from RNA templates.</p>Fórmula:C2H6O3SPureza:(Titration) 68.0 To 72.0%Forma y color:Clear LiquidPeso molecular:110.13 g/molBis[(pinacolato)boryl]methane
CAS:<p>Bis[(pinacolato)boryl]methane is a bifunctional organoboron reagent with an allyl group on one end and a cyclopropane on the other end. It is useful in organic synthesis as a nucleophile for allylation, as well as for the synthesis of unsymmetrical cyclopropanes. This compound can be used to catalyze asymmetric methods, such as the synthesis of alicyclic compounds. Bis[(pinacolato)boryl]methane can also be used to synthesize biomolecules.</p>Fórmula:C13H26B2O4Pureza:Min. 95%Forma y color:White To Off-White SolidPeso molecular:267.97 g/moltert-Butyl 3-bromopropionate
CAS:<p>Tert-butyl 3-bromopropionate is a linker for the synthesis of pleuromutilin derivatives. It has been used as a model substrate for studying the effects of hypertrophy on cardiac muscle. Tert-butyl 3-bromopropionate has also been shown to inhibit the production of proinflammatory cytokines in response to bacterial infection, and can be used as an antibacterial agent. Tert-butyl 3-bromopropionate binds to RNA and inhibits protein synthesis, which leads to cell death by preventing the production of proteins vital for cell division. Tert-butyl 3-bromopropionate is also a potent inhibitor of chloride channels that are found in nerve cells and prevents the flow of chloride ions through these channels, leading to paralysis. This drug also inhibits hydrogen fluoride excretion in rats, which may be due to its ability to bind with chloride ions in the kidney tubules, preventing their</p>Fórmula:C7H13BrO2Pureza:Min. 95%Forma y color:Colorless Clear LiquidPeso molecular:209.08 g/molN-Methyl-1,1,1-trifluoro-2-propylamine hydrochloride
CAS:<p>Please enquire for more information about N-Methyl-1,1,1-trifluoro-2-propylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Fórmula:C4H9ClF3NPureza:Min. 95%Peso molecular:163.57 g/mol1-Docosanol
CAS:<p>Docosanol is a drug that is used for the treatment of various skin disorders, including psoriasis, eczema, and ichthyosis. It is also used as an adjuvant in the treatment of chronic obstructive pulmonary disease. Docosanol is a lipid molecule that has been shown to have antiviral, antibacterial, antifungal, and antiprotozoal properties. It can be used as a carrier for topical medications and has been shown to have anti-inflammatory effects. The mechanism of action for docosanol is not well understood but may involve its ability to bind to Toll-like receptors on macrophages and neutrophils in the skin. This binding inhibits the synthesis of inflammatory mediators such as prostaglandins and leukotrienes. Docosanol also has physiological effects on water balance by acting as a surfactant in the lungs and preventing water vapor from escaping through respiratory membranes in the nose or mouth. Docosanol</p>Fórmula:C22H46OPureza:Min. 95%Forma y color:PowderPeso molecular:326.6 g/molTrifluoromethanesulfonic acid
CAS:<p>Trifluoromethanesulfonic acid is a strong oxidizing agent that is used as a catalyst for the synthesis of organic compounds. It is an excellent solvent for many types of reactions and has been shown to be an effective catalyst for the synthesis of triflate, which can be used in cationic polymerization. Trifluoromethanesulfonic acid also has potential applications in carbohydrate chemistry and asymmetric synthesis, due to its ability to reduce carboxylic acids and nitriles. Trifluoromethanesulfonic acid can be synthesized by reacting potassium hexafluorophosphate with amines or nitrogen atoms under activated conditions.</p>Fórmula:CHF3O3SPureza:Min. 95%Forma y color:Clear LiquidPeso molecular:150.08 g/molParaffin oil
CAS:<p>Paraffin oil is a mixture of hydrocarbons that is liquid at room temperature and pressure. It has been shown to inhibit the growth of human osteosarcoma cells in vitro, with a potency corresponding to that of delphinidin, a natural compound found in plants. Paraffin oil also has an inhibitory effect on the mitochondrial membrane potential and on the release of pro-inflammatory cytokines such as TNF-α and IL-6 by HL-60 cells. This inhibition may be due to the ability of paraffin oil to bind to Toll-like receptors (TLRs). The molecular mechanism underlying this inhibition remains unknown. Paraffin oil can be used as a model system for epigenetic modulators because it induces histone acetylation, which alters gene expression.</p>Pureza:Min. 95%Diiodomethane
CAS:<p>Diiodomethane is a chemical compound with the molecular formula CHI. It is a colorless gas that can be obtained by reacting methyl ethyl and hydroxyl group in the presence of an oxidant such as boron nitride. Diiodomethane has been used as a substrate film for n-dimethyl formamide and reaction solution, which have been studied using spectroscopic data. The product of this reaction is water vapor that leaves the system due to its low boiling point. Reaction mechanism for this process is thought to be due to the kinetic energy of the particles that collide and produce diiodomethane molecules.</p>Fórmula:CH2I2Pureza:Min. 95%Forma y color:Yellow Clear LiquidPeso molecular:267.84 g/mol1,3-Propanediol
CAS:<p>aliphatic diol. It has been shown to have an inhibitory effect on bacterial growth</p>Fórmula:C3H8O2Pureza:Min. 95%Forma y color:Colorless Clear LiquidPeso molecular:76.09 g/molChloroiodomethane, stabilised with copper
CAS:<p>Chloroiodomethane is a chemical that is used as an intermediate in the production of other chemicals. It is a colourless liquid with a strong odour. 3-Bromopropylamine hydrobromide reacts with chloroiodomethane to form 3-bromopropyl bromide, which can be reacted with hydrogen chloride to form the corresponding acid chloride. This reaction product can then be reacted with β-amino acids to form amides or esters. The reaction mechanism of this process involves nucleophilic substitution of chloroiodomethane by the amino group of the β-amino acid to produce an intermediate α,β-unsaturated carbonyl chloride, which undergoes elimination to give the final product. Chloroiodomethane also reacts rapidly with fatty acids and hydroxyl groups in biological systems, leading to inflammatory diseases such as HIV infection.</p>Fórmula:CH2ClIPureza:Min. 95%Forma y color:Colorless Clear LiquidPeso molecular:176.38 g/mol
