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| Product | Description | |
|---|---|---|
| aliphatic aldoxime dehydratase | The enzyme from Pseudomonas chlororaphis contains Ca2+ and protoheme IX, the iron of which must be in the form Fe(II) for activity. The enzyme exhibits a strong preference for aliphatic aldoximes, such as butyraldoxime and acetaldoxime, over aromatic aldoximes, such as pyridine-2-aldoxime, which is a poor substrate. No activity was found with the aromatic aldoximes benzaldoxime and pyridine-4-aldoxime. Group: Enzymes. Synonyms: OxdA; aliphatic aldoxime hydro-lyase. Enzyme Commission Number: EC 4.99.1.5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5362; aliphatic aldoxime dehydratase; EC 4.99.1.5; OxdA; aliphatic aldoxime hydro-lyase. Cat No: EXWM-5362. |  |
| aliphatic nitrilase | Preferentially hydrolyses aliphatic nitriles, some of which are apparently not substrates for other known nitrilases (EC 3.5.5.1). Substrates include crotononitrile, acrylonitrile and glutaronitrile. Group: Enzymes. Enzyme Commission Number: EC 3.5.5.7. CAS No. 395644-15-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4583; aliphatic nitrilase; EC 3.5.5.7; 395644-15-2. Cat No: EXWM-4583. | |
| aliphatic (R)-hydroxynitrile lyase | The enzyme contains Zn2+. The enzyme catalyses the stereoselective synthesis of aliphatic (R)-cyanohydrins. No activity towards mandelonitrile and 4-hydroxymandelonitrile. Natural substrates for the (R)-oxynitrilase from Linum usitatissimum are acetone and butan-2-one, which are the building blocks of the cyanogen glycosides in Linum, linamarin and lotaustralin, or linustatin and neolinustatin, respectively. Group: Enzymes. Synonyms: (R)-HNL; (R)-oxynitrilase; (R)-hydroxynitrile lyase; LuHNL. Enzyme Commission Number: EC 4.1.2.46. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4882; aliphatic (R)-hydroxynitrile lyase; EC 4.1.2.46; (R)-HNL; (R)-oxynitrilase; (R)-hydroxynitrile lyase; LuHNL. Cat No: EXWM-4882. | |
| Aliphatic solvents | Our wide distribution network, with locations coast-to-coast, helps guarantee fast, reliable service to Univar's customers. |  |
| C5 Aliphatic Hydrocarbon Resin Used in Adhesives Purified 99.9%min | C5 Aliphatic Hydrocarbon Resin Used in Adhesives Purified 99.9%min. Group: Aliphatic resins. |  |
| Chlorine containing aliphatic polyphosphate | Cas No. 184530-92-5. |  |
| Chlorine containing aliphatic polyphosphatephosphonate | Cas No. 67063-84-7. | |
| D-Sorbitol polyglycidyl ether - aliphatic polyfunctional epoxy resin | D-Sorbitol polyglycidyl ether - aliphatic polyfunctional epoxy resin. Uses: Designed for use in research and industrial production. Appearance: Colourless to yellow liquid. CAS No. 68412-01-1. Molecular formula: C6H14O6·C3H5ClO. Mole weight: 274.7. Product ID: ACM68412011. Alfa Chemistry ISO 9001:2015 Certified. Categories: 2-(chloromethyl)oxirane;(2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol. |  |
| EMEROX® 14270 Aliphatic Rigid Grade Polyol | Workhorse aliphatic rigid grade polyol. Functionality performs similar to SG 360 type polyether polyol. Low viscosity and hydrophobic. USDA Certified Biobased Product 99%.. Uses: Excellent in geotechnical rigid foam applications. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14270. Approvals: USDA Certified Biobased Product 99%.. Pack Sizes: Drums, Totes, Bulk Supply. |  |
| EMEROX® 14280 Aliphatic Rigid Grade Polyol | Lower hydroxyl value aliphatic rigid grade polyol with low viscosity with good functionality. Used in water blown formulations to maintain A: B ratio. USDA Certified Biobased Product 99%.. Uses: Water blown rigid foam formulations. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14280. Approvals: USDA Certified Biobased Product 99%.. Pack Sizes: Drums, Totes, Bulk Supply. | |
| EMEROX® 14355 Aliphatic Rigid Grade Polyol | Excellent low temperature stability aliphatic rigid grade polyol. Functionally performs similar to SG 360 type polyether polyol. Hydrophobic. USDA Certified Biobased Product 99%.. Uses: Excellent in geotechnical rigid foam applications. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14355. Approvals: USDA Certified Biobased Product 99%.. Pack Sizes: Drums, Totes, Bulk Supply. | |
| EMEROX® 14371 Aliphatic Rigid Grade Polyol | Higher functionality aliphatic rigid grade polyol with hydrophobic properties. USDA Certified Biobased Product 99%.. Uses: Engineered to be used as the sole polyol in PiP and spray foams. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14371. Approvals: USDA Certified Biobased Product 99%.. Pack Sizes: Drums, Totes, Bulk Supply. | |
| EMEROX® 14372 Aliphatic Rigid Grade Polyol | Very high functionality and hydrophobic aliphatic rigid grade polyol. Used primarily as a co-polyol with enhanced functionality to provide improved foam mechanical properties. USDA Certified Biobased Product 99%.. Uses: Primarily as a co-polyol in rigid foam applications. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14372. Approvals: USDA Certified Biobased Product 99%.. Pack Sizes: Drums, Totes, Bulk Supply. | |
| Methacrylated aliphatic urethane oligomer | Methacrylated aliphatic urethane oligomer. Uses: Designed for use in research and industrial production. Additional or Alternative Names: to-1-(isocyanatomethyl)-1,3,3-trimethylcyclohexane,hydroxyethylmethacrylate-b;METHACRYLATED ALIPHATIC URETHANE OLIGOMER;METHACRYLATED ALIPHATIC URETHANE (OLIGOMER) FUNCTIONALITY 2;Poly(oxy-1,4-butanediyl), alpha-hydro-omega-hydroxy-, polymer with 5-isoc. Product Category: Heterocyclic Organic Compound. CAS No. 82339-26-2. Molecular formula: C33H57N3O11. Product ID: ACM82339262. Alfa Chemistry ISO 9001:2015 Certified. | |
| N-acyl-aliphatic-L-amino acid amidohydrolase | Contains Zn2+. The enzyme is found in animals and is involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate). It acts on mercapturic acids (S-conjugates of N-acetyl-L-cysteine) and neutral aliphatic N-acyl-α-amino acids. Some bacterial aminoacylases demonstrate substrate specificity of both EC 3.5.1.14 and EC 3.5.1.114. cf. EC 3.5.1.15, aspartoacylase and EC 3.5.1.114, N-acyl-aromatic-L-amino acid amidohydrolase. Group: Enzymes. Synonyms: aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoa. Enzyme Commission Number: EC 3.5.1.14. CAS No. 9012-37-7. ACY1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4403; N-acyl-aliphatic-L-amino acid amidohydrolase; EC 3.5.1.14; 9012-37-7; aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase. Cat No: EXWM-4403. | |
| Sulfonated Aliphatic Polyester | Sulfonated Aliphatic Polyester. Uses: Designed for use in research and industrial production. Additional or Alternative Names: bu-cerumen;Butanedioicacid,sulfo-,1,4-dioctylester,sodiumsalt;di-n-octylsodiumsulfosuccinate;dioktylestersulfojantaranusodneho;elfanol883;monawetmo-70;monawetmo-70rp;monawetmo-84r2w. Product Category: Anionic Surfactants. CAS No. 1639-66-3. Molecular formula: C20H37O7S?Na. Mole weight: 444.561. Density: 1.098 g/cm³. Product ID: ACM1639663. Alfa Chemistry ISO 9001:2015 Certified. | |
| 1,1,1,11-Tetrachloroundecane | 1,1,1,11-tetrachloroundecane has been employed in the prediction of carcinogenicity and chronic toxicity of halo-substituted aliphatic hydrocarbons and is a persistant environmental pollutant. Group: Biochemicals. Grades: Highly Purified. CAS No. 3922-34-7. Pack Sizes: 1mg, 5mg. Molecular Formula: C11H20Cl4, Molecular Weight: 294.089999999999. US Biological Life Sciences. |  Worldwide |
| 1,1,1-Trimethoxy-n-octane | 1,1,1-Trimethoxyoctane is an aliphatic hydrocarbon compound with a molecular formula of C8H18O3. It is a colorless liquid that is soluble in both organic and aqueous solvents. Uses: 1,1,1-trimethoxyoctane is used in a variety of scientific applications, including in the synthesis of other compounds, as a reagent for organic reactions, and as a solvent for chromatography. additionally, it is used in the production of pesticides and has been studied for its biochemical and physiological effects. Additional or Alternative Names: 3,3,3-trimethoxyoctane. Product Category: Heterocyclic Organic Compound. Appearance: colorless liquid. CAS No. 161838-87-5. Molecular formula: C11H24O3. Mole weight: 204.31. Purity: 0.96. IUPACName: 1,1,1-trimethoxyoctane. Canonical SMILES: CCCCCCCC(OC)(OC)OC. Product ID: ACM161838875. Alfa Chemistry ISO 9001:2015 Certified. | |
| 1,12-Diaminododecane | 1,12-Diaminododecane is a long aliphatic diamine that is known to inhibit specific phospholipid-sensitive enzymes and myosin light-chain kinases. Group: Biochemicals. Grades: Highly Purified. CAS No. 2783-17-7. Pack Sizes: 5g, 25 g. Molecular Formula: C12H28N2, Molecular Weight: 200.36. US Biological Life Sciences. | Worldwide |
| (±)-1,2-Propanediol | (±)-1, 2-propanediol (1,2-(RS)-Propanediol) is an aliphatic alcohol that is often used as an excipient in many active molecular preparations to increase the solubility and stability of the active molecule. (±)-1, 2-propanediol can affect the neurobehavior of zebrafish [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: 1,2-(RS)-Propanediol; 1,2-Propylene glycol; Propylene glycol. CAS No. 57-55-6. Pack Sizes: 100 mL. Product ID: HY-Y0921. |  |
| (±)-1,2-Propanediol | USP grade. Uses: (±)-1,2-propanediol is an aliphatic alcohol and frequently used as an excipient in many drug formulations to increase the solubility and stability of drugs. Additional or Alternative Names: Propylene glycol, (±)-1,2-Propylene glycol, 1,2-Dihydroxypropane, 1,2-Propanediol, (±)-1,2-Dihydroxy propane. Product Category: Solvents. CAS No. 57-55-6. Molecular formula: CH3CH(OH)CH2OH. Mole weight: 76.1. Canonical SMILES: CC(O)CO. Density: 1.0±0.1 g/cm3. ECNumber: 200-338-0. Product ID: ACM57556-9. Alfa Chemistry ISO 9001:2015 Certified. | |
| 142 Solvent | 142 Solvent. Category ALIPHATIC SOLVENTS. Pack Sizes Bulk/ Drums |  |
| 1,4-Butanediol Diglycidyl Ether, 98% | For post-crosslinking reactions, preparation of aliphatic epoxy resins. Group: Biochemicals. Alternative Names: 1, 4-Bis(2, 3-epoxypropoxy)butane;1, 4-Diglycidyloxybutane; Tetramethylene Glycol Diglycidyl Ether. Grades: Highly Purified. CAS No. 2425-79-8. Pack Sizes: 50g, 100g, 250g, 500g, 1Kg. Molecular Formula: C10H18O4, Molecular Weight: 202.25. US Biological Life Sciences. | Worldwide |
| 1, 4-Diazabicyclo[2. 2. 2]octane | 1, 4-Diazabicyclo[2. 2. 2]octane is an aliphatic amine that is used as a catalyst in organic synthesis. Group: Biochemicals. Grades: Highly Purified. CAS No. 280-57-9. Pack Sizes: 2.5g, 10g. Molecular Formula: C6H12N2. US Biological Life Sciences. | Worldwide |
| 1,4-lactonase | The enzyme is specific for 1,4-lactones with 4-8 carbon atoms. It does not hydrolyse simple aliphatic esters, acetylcholine, sugar lactones or substituted aliphatic lactones, e.g. 3-hydroxy-4-butyrolactone; requires Ca2+. Group: Enzymes. Synonyms: γ-lactonase. Enzyme Commission Number: EC 3.1.1.25. CAS No. 37278-38-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3450; 1,4-lactonase; EC 3.1.1.25; 37278-38-9; γ-lactonase. Cat No: EXWM-3450. | |
| 1,5-Dimethylhexylamine | 1,5-Dimethylhexylamine is an aliphatic secondary amine which shows leucine aminotransferase inhibition. 1,5-Dimethylhexylamine is used in the preparation of glycosyl β-amino acids with antitubercular activity. Group: Biochemicals. Alternative Names: (±)-1,5-Dimethylhexylamine; (±)-2-Amino-6-methylheptane; (±)-6-Methyl-2-heptanamine; 1,5-Dimethylhexanamine; 1,5-Dimethylhexylamine; 2-Amino-6-methylheptane; 2-Isooctylamine; 2-Methyl-6-aminoheptane; 6-Amino-2-methylheptane; 6-Methyl-2-heptanamine; 6-Methyl-2-heptylamine; Amidrine; Isoctaminum; Octodrin; Octodrine; SKF 51; Vaporpac; dl-2-Amino-6-methylheptane; dl-2-Isooctylamine; α,ε-Dimethylhexylamine. Grades: Highly Purified. CAS No. 543-82-8. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| 1,5-Dimethylhexylamine Hydrochloride | 1,5-Dimethylhexylamine Hydrochloride is an aliphatic secondary amine which shows leucine aminotransferase inhibition. 1,5-Dimethylhexylamine Hydrochloride is used in the preparation of glycosyl β-amino acids with antitubercular activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 5984-59-8. Pack Sizes: 1g, 5g. Molecular Formula: C8H20ClN. US Biological Life Sciences. | Worldwide |
| 1-Bromo-2,4-dinitrobenzene-d3 | 1-Bromo-2,4-dinitrobenzene-d3 is an intermediate in the synthesis of dinitrophenylhydrazone (DNPH) derivatives of an aliphatic aldehyde found in mainstream cigarette smoke. Group: Biochemicals. Grades: Highly Purified. CAS No. 1313734-81-4. Pack Sizes: 100mg, 1g. Molecular Formula: C6D3BrN2O4. US Biological Life Sciences. | Worldwide |
| 1-Cyclohexenylalde hyde1192-88-7 | 1-Cyclohexenylaldehyde can be used as reactant/reagent in chemoselective synthesis of aliphatic alcohols via NSS-ruthenium complex-catalyzed hydrogenation of α, β-unsaturated carbonyl compounds. Group: Biochemicals. Grades: Highly Purified. CAS No. 1192-88-7. Pack Sizes: 50mg, 250mg. Molecular Formula: C7H10O, Molecular Weight: 110.15. US Biological Life Sciences. | Worldwide |
| 1-Cycloocten-1-ol 1-Acetate | 1-Cycloocten-1-ol 1-Acetate is a derivative of cyclooctanone (C988345), a aliphatic cycle that exhibited inhibitory activity towards aldosterone synthase, a promising therapeutic target for the treatment of cardiovascular diseases related to abnormally high aldosterone level. Group: Biochemicals. Alternative Names: 1-Cycloocten-1-ol Acetate; 1-Acetoxycyclooctene; 1-Cycloocten-1-yl Acetate; 1-Cyclooctenyl Acetate. Grades: Highly Purified. CAS No. 14478-13-8. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| 1-Octacosanol | 1-Octacosanol is a straight-chain aliphatic 28-carbon fatty alcohol with well-known anti-fatigue function [1]. Uses: Scientific research. Group: Natural products. CAS No. 557-61-9. Pack Sizes: 50 mg; 100 mg. Product ID: HY-N6811. | |
| 2,2,2-Trifluoroethyl Chloroformate | 2,2,2-Trifluoroethyl chloroformate is a derivatization reagent used to produce primary and secondary aliphatic amines (e.g. N-Methylhexadecylamine [M311995]). Group: Biochemicals. Grades: Highly Purified. CAS No. 27746-99-2. Pack Sizes: 1g, 10g. Molecular Formula: C3H2ClF3O2, Molecular Weight: 162.49. US Biological Life Sciences. | Worldwide |
| 2,2,4-Trimethyl-1-pentanol | 2,2,4-Trimethyl-1-pentanol is an aliphatic alcohol producing a fruity odor and used in the food industry as an additive. Group: Biochemicals. Grades: Highly Purified. CAS No. 123-44-4. Pack Sizes: 10mg, 50mg. Molecular Formula: C8H18O, Molecular Weight: 130.229999999999. US Biological Life Sciences. | Worldwide |
| 230 Solvent | 230 Solvent. Category ALIPHATIC SOLVENTS. Pack Sizes Bulk/ Drums | |
| 2-Amino-5-methylhexane | 2-Amino-5-methylhexane is an aliphatic amine used in the preparation of pyridines and other cyclic nitrogen based compounds for use ranging from antiparasitics to calcium channel inhibitors. Group: Biochemicals. Alternative Names: (±)-2-Amino-5-methylhexane; 1,4-Dimethylpentylamine; 5-Methyl-2-hexylamine; NSC 73708; dl-2-Amino-5-methylhexane. Grades: Highly Purified. CAS No. 28292-43-5. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 2-[Boc (2-Bocaminoethyl) amino]ethanol | 2-[Boc (2-Bocaminoethyl) amino]ethanol is an intermediate in the synthesis of spermidine (S680400) and analogous triamines of the aliphatic series. Group: Biochemicals. Grades: Highly Purified. CAS No. 200283-08-5. Pack Sizes: 5mg, 25mg. Molecular Formula: C14H28N2O5. US Biological Life Sciences. | Worldwide |
| 2-Butanone-13C3 2,4-Dinitrophenylhydrazone | Isotope labelled 2-Butanone 2,4-Dinitrophenylhydrazone is a dinitrophenylhydrazone (DNPH) derivative of an aliphatic ketone found in mainstream cigarette smoke. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C713C3H12N4O4, Molecular Weight: 255.2. US Biological Life Sciences. | Worldwide |
| 2-Butanone-13C6 2,4-Dinitrophenylhydrazone | Isotope labelled 2-Butanone 2,4-Dinitrophenylhydrazone is a dinitrophenylhydrazone (DNPH) derivative of an aliphatic ketone found in mainstream cigarette smoke. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C413C6H12N4O4, Molecular Weight: 258.18. US Biological Life Sciences. | Worldwide |
| (2-Chloro-4-tri fluoromethoxyphenyl) Boronic Acid | (2-Chloro-4-tri fluoromethoxyphenyl) Boronic Acid is an intermediate used to prepare aza- and diazabiphenyl analogs of the antitubercular drug (6S) -2-nitro-6-{[4- (trifluoromethoxy) benzyl]oxy}-6, 7-dihydro-5H-imidazo[2, 1-b][1, 3]oxazine. It is also used in the synthesis of aryl (alkylamino) nitropyridines via amination of chloro hydroxynitropyridine with aliphatic amines followed by chlorination, and Suzuki-coupling with arylboronic acids. Group: Biochemicals. Grades: Highly Purified. CAS No. 345226-20-2. Pack Sizes: 100mg, 500mg. Molecular Formula: C7H5BClF3O3, Molecular Weight: 240.37. US Biological Life Sciences. | Worldwide |
| 2-Ethyl-2-methoxyhexyl Salicylate | 2-Ethyl-2-methoxyhexyl Salicylate is made from 3-Heptanone which is versatile synthetic building block. It was used in the synthesis of semicarbazone and thiosemicarbazone derivatives with antimalarial activity. 3-Heptanone was also used as reactant in enantioselective organocatalytic reductive amination of aliphatic ketones with aromatic amines using benzothiazoline hydrogen donor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 25mg. Molecular Formula: C16H24O4, Molecular Weight: 280.36. US Biological Life Sciences. | Worldwide |
| 2-hydroxy-4-carboxymuconate semialdehyde hemiacetal dehydrogenase | The enzyme does not act on unsubstituted aliphatic or aromatic aldehydes or glucose; NAD+ can replace NADP+, but with lower affinity. The enzyme was initially believed to act on 4-carboxy-2-hydroxy-cis,cis-muconate 6-semialdehyde and produce 4-carboxy-2-hydroxy-cis,cis-muconate. However, later studies showed that the substrate is the hemiacetal form, and the product is 2-oxo-2H-pyran-4,6-dicarboxylate. Group: Enzymes. Synonyms: 2-hydroxy-4-carboxymuconate 6-semialdehyde dehydrogenase; 4-carboxy-2-hydroxy-cis,cis-muconate-6-semialdehyde:NADP+ oxidoreductase; α-hydroxy-γ-carboxymuconic ε-semialdehyde dehydrogenase; 4-carboxy-2-hydroxymuconate-6-semialdehyde dehydrogenase; LigC; ProD. Enzyme Commission Number: EC 1.1.1.312. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0224; 2-hydroxy-4-carboxymuconate semialdehyde hemiacetal dehydrogenase; EC 1.1.1.312; 2-hydroxy-4-carboxymuconate 6-semialdehyde dehydrogenase; 4-carboxy-2-hydroxy-cis,cis-muconate-6-semialdehyde:NADP+ oxidoreductase; α-hydroxy-γ-carboxymuconic ε-semialdehyde dehydrogenase; 4-carboxy-2-hydroxymuconate-6-semialdehyde dehydrogenase; LigC; ProD. Cat No: EXWM-0224. | |
| 2-(Methyl-d3)-butanoic-2,3,3,4,4,4-d6 Acid | 2-(Methyl-d3)-butanoic-2,3,3,4,4,4-d6 Acid is labelled DL-2-Methylbutyric Acid (M294865) which is a common chemical reagent used in the synthesis of anticancer naphthoquinione aliphatic amides. Also used in the synthesis of novel erythromycins. Group: Biochemicals. Grades: Highly Purified. CAS No. 352431-44-8. Pack Sizes: 50mg, 100mg. Molecular Formula: C5HD9O2, Molecular Weight: 111.19. US Biological Life Sciences. | Worldwide |
| 2-(Perfluorohexyl)ethyl Thiocyanate | 2-(Perfluorohexyl)ethyl Thiocyanate is an intermediate in synthesizing 3, 3, 4, 4, 5, 5, 6, 6, 7, 7, 8, 8, 8-Tridecafluorooctane-1-sulphonic Acid (), an aliphatic compound for fluorinated surfactant synthesis. Group: Biochemicals. Grades: Highly Purified. CAS No. 26650-09-9. Pack Sizes: 100mg, 250mg. Molecular Formula: C9H4F13NS. US Biological Life Sciences. | Worldwide |
| 2-?(tert-?Butylamino)?ethanol | 2-?(tert-?Butylamino)?ethanol is used in the catalytic carbonylation of aliphatic amines to beta-lactams. Group: Biochemicals. Grades: Highly Purified. CAS No. 4620-70-6. Pack Sizes: 1g, 5g. Molecular Formula: C6H15NO, Molecular Weight: 117.19. US Biological Life Sciences. | Worldwide |
| 3,4-Epoxycyclohexylmethyl 3,4-Epoxycyclohexanecarboxylate | 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate (EEC) is a cycloaliphatic epoxy that can be synthesized by the reaction of 3'-cyclohexenylmethyl 3-cyclohexenecarboxylate with peracetic acid. Its aliphatic backbone and molecular structure provide a number of useful properties such as thermal stability, weatherability, and electrical conductivity. Uses: Eec is an epoxy monomer that can be used as a resin in aerospace, electronics and automobile industries as an adhesive and a composite material. Group: Monomers. Alternative Names: 7-Oxabicyclo[4.1.0]Heptan-3-Ylmethyl 7-Oxabicyclo[4.1.0]Heptane-3-Carboxylate. CAS No. 2386-87-0. Pack Sizes: Packaging 50, 250 mL in poly bottle. Product ID: 7-oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate. Molecular formula: 252.31. Mole weight: C14H20O4. C1CC2C(O2)CC1COC(=O)C3CCC4C(C3)O4. InChI=1S/C14H20O4/c15-14 (9-2-4-11-13 (6-9)18-11)16-7-8-1-3-10-12 (5-8)17-10/h8-13H, 1-7H2. YXALYBMHAYZKAP-UHFFFAOYSA-N. 95%+. | |
| 3,6-Dimethyl-1,4-dioxane-2,5-dione homopolymer | It is an aliphatic polyester that is considered to be a safe material and its biodegradable properties. It is primarily used as a biocompatible and biodegradable carrier for many types of human and veterinary implant or injection delivery systems. Uses: Used to make polylactic acid and cosmetics. Synonyms: Poly(DL-lactide); Lactel DL-PLA; 1,4-Dioxane-2,5-dione, 3,6-dimethyl-, homopolymer; PDLLA; Lactide polymer; Polylactide; p-Dioxane-2,5-dione, 3,6-dimethyl-, polyesters; D,L-Lactide homopolymer; D,L-Lactide-L-lactide copolymer; D-Lactide-L-lactide copolymer; DL-Lactide-D-lactide copolymer; DL-Lactide-L-lactide copolymer; DL-3,6-Dimethyl-1,4-dioxane-2,5-dione homopolymer; DL-Dilactide homopolymer; DL-Dilactide polymer; DL-Lactide homopolymer; DL-Lactide polymer; L-Lactide-D,L-lactide copolymer; L-Lactide-D-lactide copolymer; L-Lactide-DL-lactide copolymer; L-Lactide-lactide copolymer; CPX 5-2; DL-Lactide-L-lactide copolymer; Lactide homopolymer; Lactide polymer; Lactide-D-lactide copolymer; Poly(D,L-Lactide-co-L-lactide); Poly(L-lactide-co-DL-lactide); Poly(lactide); Poly-dl-lactide; Pullulan polylactide; Purasorb DL homopolymer; Purasorb PLDL 8038; rac-Lactide homopolymer; Resomer R 203S. CAS No. 26680-10-4. Molecular formula: (C6H8O4)n. | |
| 3-Acetylpyridine-Adenine Dinucleotide, Oxidized (APAD) | 3-Acetylpyridine adenine dinucleotide is an NAD analog with higher oxidation potential than NAD. It can substitute for NAD as a hydrogen-accepting cofactor in many dehydrogenase reactions. For example lactate dehydrogenase from Toxoplasma, Clonorchis, and Plasmodium, bacterial lipoamide dehydrogenase, as well as mammalian dehydrogenases. This compound can also act as a proton acceptor in various transhydrogenation reactions with NADH or NADPH. Group: Coenzymes. Synonyms: aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NA. Enzyme Commission Number: EC 1.1.1.1. CAS No. 1986-8-8. Purity: Determined by increase in absorbance at 363 nm on enzymatic reduction with ADH* at pH 10.0 > 92% *ADH = Alcohol dehydrogenase (Horse liver) (EC 1.1.1.1.). APAD. Mole weight: 662.44. Storage: Keep tightly stoppered in the dark below 5°C. Moisture will reduce the purity. For prolonged storage, keep below-20°C. aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1; APAD. Cat No: NATE-0077. | |
| 3-Acetylpyridine-Adenine Dinucleotide, Reduced (APADH) | Molecular Formula: C22H28N6O14P2. Group: Coenzymes. Synonyms: aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1; APADH. Enzyme Commission Number: EC 1.1.1.1. CAS No. 102029-93-6. Purity: Determined by decrease in absorbance at 363 nm on enzymatic oxidation with ADH* at pH 7.5 (> 92%) *ADH = Alcohol dehydrogenase (horse liver) (EC 1.1.1.1.). APADH. Mole weight: 708.42. Storage: Keep tightly stoppered in the dark below-20°C. Moisture will reduce the purity. For Prolonged storage, keep below-80°C. aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1; APADH. Cat No: NATE-0078. | |
| 3-Azido-L-alanine hydrochloride | 3-Azido-L-alanine hydrochloride is an aliphatic functionalized amino acid with side chain lengths of up to four carbons [1]. 3-Azido-L-alanine (hydrochloride) is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. Uses: Scientific research. Group: Signaling pathways. CAS No. 1620171-64-3. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-W336328. | |
| 3-Bromo-4-fluoro-5-nitrobenzoic Acid | 3-Bromo-4-fluoro-5-nitrobenzoic Acid is a derivative of m-Nitrobenzoic Acid (N494700), a reagent used in the coupling of allyl acetate to allylic, aliphatic and benzylic alcohols. Group: Biochemicals. Grades: Highly Purified. CAS No. 1290117-21-3. Pack Sizes: 250mg, 500mg. Molecular Formula: C7H3BrFNO4, Molecular Weight: 264.01. US Biological Life Sciences. | Worldwide |
| (3-Bromopropyl)phosphonic Acid | (3-Bromopropyl)phosphonic Acid is a reagent used in the synthesis of amino-substituted aromatic and aliphatic phosphonic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 1190-09-6. Pack Sizes: 100mg, 500mg. Molecular Formula: C3H8BrO3P, Molecular Weight: 202.97. US Biological Life Sciences. | Worldwide |
| 3-Buten-1-ol | 3-Buten-1-ol is an aliphatic primary alcohol used as a reagent in organic synthesis. Group: Biochemicals. Alternative Names: 1-Buten-4-ol; 1-Hydroxy-3-butene; 3-Butenyl Alcohol; 4-Hydroxy-1-butene; Allylcarbinol; Homoallyl Alcohol; NSC 60194; β-Vinylethanol. Grades: Highly Purified. CAS No. 627-27-0. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| 3-Buten-1-ol | 3-Buten-1-ol is an aliphatic primary alcohol used as a reagent in organic synthesis. Uses: 3-buten-1-ol is an aliphatic primary alcohol used as a reagent in organic synthesis. Additional or Alternative Names: 4-Hydroxy-1-butene; V6966; 79116-EP2305698A2; PubChem18909; UNII-3DB2KRM1I9; 3-Buten-1-O1; 627-27-0; ZINC1530356; KSC353Q2N; NSC60194. Product Category: Alkenes. Appearance: Clear colorless liquid. CAS No. 627-27-0. Molecular formula: C4H8O. Mole weight: 72.107g/mol. IUPACName: but-3-en-1-ol. Canonical SMILES: C=CCCO. Density: 0.838. ECNumber: 210-991-3. Product ID: ACM627270. Alfa Chemistry ISO 9001:2015 Certified. | |
| 3-Fluorobenzotrifluoride | 3-Fluorobenzotrifluoride is a fluorniated toluene used in photochemical reactions with aliphatic amines as well as in photocycloaddition reactions. Group: Biochemicals. Alternative Names: 1-Fluoro-3- (trifluoromethyl) benzene; 3-Fluoro (trifluoromethyl) benzene; NSC 10315; Trifluoromethyl-3-fluorobenzene; m, α, α, α-Tetrafluorotoluene; m- (Trifluoromethyl) fluorobenzene; m-Fluoro (trifluoromethyl) benzene; m-Fluorobenzotrifluoride ; α, α, α, 3-Tetrafluorotoluene. Grades: Highly Purified. CAS No. 401-80-9. Pack Sizes: 50g. US Biological Life Sciences. | Worldwide |
| 4-(Tetrahydropyran-2-yloxy)-1-butene | 4-(Tetrahydropyran-2-yloxy)-1-butene is a protected derivative of 3-Buten-1-ol (B689990), an aliphatic primary alcohol used as a reagent in organic synthesis. Group: Biochemicals. Alternative Names: 2-(3-Butenyloxy)tetrahydro-2H-pyran; 2-(3-Buten-1-yloxy)tetrahydro-2H-pyran; NSC 266086. Grades: Highly Purified. CAS No. 59574-65-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 5(6)-CFDA | 5(6)-CFDA is a common aliphatic luciferin-line organism. CFDA conducts free diffusion into cells, and then it is hydrolyzed into carboxyl fluorescein (CF) by intracellular non-specific lipase. CF containing portion contains an additional negative charge so that it is better retained in cells, compared to fluorescein dyes [1] [2] [3]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: 5-(6)-Carboxyfluorescein diacetate; CFDA. CAS No. 124387-19-5. Pack Sizes: 50 mg; 100 mg. Product ID: HY-D0722. | |
| 5-Amino-1-pentanol | 5-Amino-1-pentanol is an aliphatic amino alcohol with potential plasma lipid-lowering properties. 5-Amino-1-pentanol and other amino alcohols are used as emulsifying agents in dry-cleaning soaps, wax removers, cosmetics, paints and insecticides. Group: Biochemicals. Alternative Names: 1-Amino-5-hydroxypentane; 1-Amino-5-pentanol; 5-Aminopentanol; 5-Hydroxy-1-pentanamine; 5-Hydroxypentylamine; Pentanolamine. Grades: Highly Purified. CAS No. 2508-29-4. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| 5-CFDA | 5-CFDA is a common aliphatic luciferin-line organism. CFDA conducts free diffusion into cells, and then it is hydrolyzed into carboxyl fluorescein (CF) by intracellular non-specific lipase. CF containing portion contains an additional negative charge so that it is better retained in cells, compared to fluorescein dyes [1] [2] [3]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: 5-Carboxyfluorescein diacetate. CAS No. 79955-27-4. Pack Sizes: 50 mg. Product ID: HY-D0047. | |
| [6,6]-Phenyl-C61 butyric acid butyl ester | [6,6]-Phenyl-C61 butyric acid butyl ester ([60]PCB-C4) is a fullerene derivative that is used as an acceptor molecule with good field effect mobility in organic electronics. It has a structural similarity to PCBM based fullerene and its aliphatic groups facilitate an increase in its solubility. Uses: [60]pcb-c4 is a conducting polymer, which can be used in a variety of applications such as organic photovoltaic cells (opvs) and bulk heterojunction (bhj) solar cells. Group: Carbon nano materials organic field effect transistor (ofet) materials organic solar cell (opv) materials. Alternative Names: 1-(3-Butoxycarbonylpropyl)-1-phenyl-[6.6]C61,PCBB,PCB-C4. CAS No. 571177-66-7. Pack Sizes: 1 g in glass bottle. Product ID: butyl 4-[(28S, 30R)-29-phenyl-29-heptadecacyclo[10.8.8.813, 17.55, 28.04, 22.08, 32.09, 30.016, 40.020, 35.021, 36.023, 33.024, 37.025, 31.026, 38.027, 41.028, 30.034, 39]hentetraconta-1(20), 2, 4, 6, 8, 10, 12, 14, 16, 18, 21, 23, 25(31), 26, 32, 34, 36, 38, 40-nonadecaenyl]butanoate. Molecular formula: 952.96. Mole weight: C55H30O2. CCCCOC (=O) CCCC2 (c1ccccc1) C34c5c6c7c8c9c% 10c (c% 11c% 12c3c% 13c5c% 14c% 15c6c% 16c7c% 17c9c% 18c% 19c% 10c% 20c% 11c% 21c% 12c% 22c% 13c% 23c% 14c% 24c% 15c% 25c% 16c% 26c% 17c% 18c% 27c% 28c% 19c% 20c% 29c% 21c% 30c% 22c% 23c% 31c% 24c% 32c% 25c% 26c% 27c% 33c% 28c% 29c% 30c% 31c% 32% 33) C248. InChI= 1S / C55H30O2 / c1-2-3-22-57-34 (56) 10-7-21-5 | |
| 6-CFDA | 6-CFDA is a common aliphatic luciferin-line organism. CFDA conducts free diffusion into cells, and then it is hydrolyzed into carboxyl fluorescein (CF) by intracellular non-specific lipase. CF containing portion contains an additional negative charge so that it is better retained in cells, compared to fluorescein dyes [1] [2] [3] [4]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: 6-Carboxyfluorescein diacetate. CAS No. 3348-3-6. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-D0721. | |
| 7-Aminoheptanoic acid | 7-Aminoheptanoic Acid is an aliphatic ω-amino acid that acts as a ligand for recombinant kringle 2 domain (residues 180-261) of human tissue-type plasminogen. Synonyms: 7-Ahp-OH; 7-Aminoenanthic acid; omega-Aminoenantic acid; 7-Amino-heptanoic acid; HEPTANOIC ACID, 7-AMINO-; 7-Aminohepentanoic acid; Aminoenanthic acid; Amino-enanthylic acid; omega-Aminoheptanoic acid. Grades: ≥ 99%. CAS No. 929-17-9. Molecular formula: C7H15NO2. Mole weight: 145.20. | |
| Acetone 2,4-Dinitrophenylhydrazone | Acetone 2,4-Dinitrophenylhydrazone is a dinitrophenylhydrazone (DNPH) derivative of an aliphatic ketone found in mainstream cigarette smoke. Acetone 2,4-Dinitrophenylhydrazone showed inhibitory activity towards soybean lipoxygenase and renal prostaglandin synthetase. Group: Biochemicals. Alternative Names: 2-Propanone 2- (2, 4-Dinitrophenyl) hydrazone; 2-Propanone (2, 4-Dinitrophenyl) hydrazone; Acetone (2, 4-Dinitrophenyl) hydrazone; 1-(2,4-Dinitrophenyl)-2-(propan-2-ylidene)hydrazine; NSC 131450; NSC 6120. Grades: Highly Purified. CAS No. 1567-89-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| alcohol dehydrogenase | A zinc protein. Acts on primary or secondary alcohols or hemi-acetals with very broad specificity; however the enzyme oxidizes methanol much more poorly than ethanol. The animal, but not the yeast, enzyme acts also on cyclic secondary alcohols. Group: Enzymes. Synonyms: aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase. Enzyme Commission Number: EC 1.1.1.1. CAS No. 9031-72-5. Alcohol dehydrogenase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0001; alcohol dehydrogenase; EC 1.1.1.1; 9031-72-5; aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase. Cat No: EXWM-0001. | |
| Alcohol dehydrogenase from E. coli, Recombinant | Alcohol dehydrogenases (ADH) are a group of dehydrogenase enzymes that occur in many organisms and facilitate the interconversion between alcohols and aldehydes or ketones with the reduction of nicotinamide adenine dinucleotide (NAD+ to NADH). In Humans and many other animals, they serve to break down alcohols that otherwise are toxic, and they also participate in geneRation of useful aldehyde, ketone, or alcohol groups during biosynthesis of various metabolites. In yeast, plants, and many bacteria, some alcohol dehydrogenases catalyze the opposite reaction as part of fermentation to ensure a constant supply of NAD+. Applications: High purity recombinant alcohol dehyd...l dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1. Enzyme Commission Number: EC 1.1.1.1. CAS No. 9031-72-5. Alcohol dehydrogenase. Mole weight: ~ 38,642 Da. Activity: 6.7 U/mg protein at pH 8.5 and 25°C. Storage: Store at 4°C. Do not store the enzyme in presence of sodium azide. Form: In 3.2 M ammonium sulphate. Source: E. coli. aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1. Cat No: NATE-0803. | |
| Alcohol dehydrogenase from Equine, Recombinant | Alcohol dehydrogenases (ADH) are a group of dehydrogenase enzymes that occur in many organisms and facilitate the interconversion between alcohols and aldehydes or ketones with the reduction of nicotinamide adenine dinucleotide (NAD+ to NADH). In Humans and many other animals, they serve to break down alcohols that otherwise are toxic, and they also participate in geneRation of useful aldehyde, ketone, or alcohol groups during biosynthesis of various metabolites. In yeast, plants, and many bacteria, some alcohol dehydrogenases catalyze the opposite reaction as part of fermentation to ensure a constant supply of NAD+. Group: Enzymes. Synonyms: aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcoh. Enzyme Commission Number: EC 1.1.1.1. CAS No. 9031-72-5. Alcohol dehydrogenase. Activity: >0.5 U/mg. Storage: Store at -20°C. Source: E. coli. Species: Equine. aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1. Cat No: NATE-1584. | |
| Alcohol dehydrogenase from Human, Recombinant | Alcohol dehydrogenases (ADH) are a group of dehydrogenase enzymes that occur in many organisms and facilitate the interconversion between alcohols and aldehydes or ketones with the reduction of nicotinamide adenine dinucleotide (NAD+ to NADH). In Humans and many other animals, they serve to break down alcohols that otherwise are toxic, and they also participate in geneRation of useful aldehyde, ketone, or alcohol groups during biosynthesis of various metabolites. In yeast, plants, and many bacteria, some alcohol dehydrogenases catalyze the opposite reaction as part of fermentation to ensure a constant supply of NAD+. Group: Enzymes. Synonyms: aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcoh. Enzyme Commission Number: EC 1.1.1.2. Alcohol dehydrogenase. Mole weight: 36573.0 Da. Source: Human. aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.2. Cat No: NATE-1197. | |
| alcohol dehydrogenase [NAD(P)+] | Reduces aliphatic aldehydes of carbon chain length from 2 to 14, with greatest activity on C4, C6 and C8 aldehydes; also reduces retinal to retinol. Group: Enzymes. Synonyms: retinal reductase (ambiguous); aldehyde reductase (NADPH/NADH); alcohol dehydrogenase [NAD(P)]. Enzyme Commission Number: EC 1.1.1.71. CAS No. 37250-10-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0355; alcohol dehydrogenase [NAD(P)+]; EC 1.1.1.71; 37250-10-5; retinal reductase (ambiguous); aldehyde reductase (NADPH/NADH); alcohol dehydrogenase [NAD(P)]. Cat No: EXWM-0355. | |
| alcohol O-acetyltransferase | Acts on a range of short-chain aliphatic alcohols, including methanol and ethanol. Group: Enzymes. Synonyms: alcohol acetyltransferase. Enzyme Commission Number: EC 2.3.1.84. CAS No. 80237-89-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2265; alcohol O-acetyltransferase; EC 2.3.1.84; 80237-89-4; alcohol acetyltransferase. Cat No: EXWM-2265. | |
| alcohol sulfotransferase | Primary and secondary alcohols, including aliphatic alcohols, ascorbic acid, chloramphenicol, ephedrine and hydroxysteroids, but not phenolic steroids, can act as acceptors (cf. EC 2.8.2.15 steroid sulfotransferase). Group: Enzymes. Synonyms: hydroxysteroid sulfotransferase; 3β-hydroxy steroid sulfotransferase; Δ5-3β-hydroxysteroid sulfokinase; 3-hydroxysteroid sulfotransferase; HST; 5α-androstenol sulfotransferase; cholesterol sulfotransferase; dehydroepiandrosterone sulfotransferase; estrogen sulfokinase; estrogen sulfotransferase; steroid alcohol sulfo. Enzyme Commission Number: EC 2.8.2.2. CAS No. 9032-76-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3378; alcohol sulfotransferase; EC 2.8.2.2; 9032-76-2; hydroxysteroid sulfotransferase; 3β-hydroxy steroid sulfotransferase; Δ5-3β-hydroxysteroid sulfokinase; 3-hydroxysteroid sulfotransferase; HST; 5α-androstenol sulfotransferase; cholesterol sulfotransferase; dehydroepiandrosterone sulfotransferase; estrogen sulfokinase; estrogen sulfotransferase; steroid alcohol sulfotransferase; steroid sulfokinase; steroid sulfotransferase; sterol sulfokinase; sterol sulfotransferase; alcohol/hydroxysteroid sulfotransferase; 3β-hydroxysteroid sulfotransferase. Cat No: EXWM-3378. | |
| alkanesulfonate monooxygenase | The enzyme from Escherichia coli catalyses the desulfonation of a wide range of aliphatic sulfonates (unsubstituted C1- to C14-sulfonates as well as substituted C2-sulfonates). Does not desulfonate taurine (2-aminoethanesulfonate) or aromatic sulfonates. Does not use FMN as a bound cofactor. Instead, it uses reduced FMN (i.e., FMNH2) as a substrate. FMNH2 is provided by SsuE, the associated FMN reductase (EC 1.5.1.38). Group: Enzymes. Synonyms: SsuD; sulfate starvation-induced protein 6; alkanesulfonate,reduced-FMN:oxygen oxidoreductase. Enzyme Commission Number: EC 1.14.14.5. CAS No. 256383-67-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0931; alkanesulfonate monooxygenase; EC 1.14.14.5; 256383-67-2; SsuD; sulfate starvation-induced protein 6; alkanesulfonate,reduced-FMN:oxygen oxidoreductase. Cat No: EXWM-0931. | |
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