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| Product | Description | |
|---|---|---|
| Albuterol sulfate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Albuterol sulfate | Albuterol sulfate. Group: Biochemicals. Alternative Names: a1-[[ (1, 1-Dimethylethyl) amino]methyl]-4-hydroxy-1, 3-benzenedimethanol sulfate; Aerolin; Albuterol hemisulfate. Grades: Highly Purified. CAS No. 51022-70-9. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C26H44N2O10S. US Biological Life Sciences. |  Worldwide |
| Albuterol Sulfate | Salbutamol Sulfate is a non-selective 2-adrenergic receptor agonist (IC50=8.93 μM). Uses: Non-selective β-adrenergic agonist. Synonyms: Salbutamol sulfate; Salbutamol hemisulfate; Albuterol hemisulfate; 1,3-Benzenedimethanol, α1-[[(1,1-dimethylethyl)amino]methyl]-4-hydroxy-, sulfate (2:1); (±)-Salbutamol sulfate; AccuNeb; Asmadil; Bronter; Buventol; Cetsim; Cobutolin; Dilatamol; dl-Salbutamol sulfate; Ecovent; Farcolin; Grafalin; Instavent; Libretin; Loftan; Medolin; Mozal; Novosalmol; NSC 289928; Parasma; Proventil; Respax; Salbetol; Theosal; Tobybron; Vencronyl; Ventorain; Volma. Grades: ≥98%. CAS No. 51022-70-9. Molecular formula: (C13H21NO3)2·H2O4S. Mole weight: 576.70. |  |
| Albuterol Sulfate (Aerolin, Asmaven, Cobutolin, Ecovent, Loftan, Proventyl, Salbulin, Salbumol) | ß-Adrenergic agonist. Group: Biochemicals. Alternative Names: Aerolin; Asmaven; Cobutolin; Ecovent; Loftan; Proventyl; Salbulin; Salbumol. Grades: Highly Purified. CAS No. 51022-70-9. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Albuterol USP Related Compound F | Albuterol USP Related Compound F. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 4-(2-(tert-butylamino)-1-ethoxyethyl)-2-(hydroxymethyl)phenol. CAS No. 1221742-55-7. Molecular formula: C15H25NO3. Mole weight: 267.36. Catalog: APB1221742557. | |
| albutrepenonacog alfa | Albutrepenonacog alfa is a long-acting recombinant coagulation factor IX albumin fusion protein. It was approved for the treatment of hemophilia B. It can reduce the risk of bleeding episodes in patients with hemophilia B. Uses: The treatment of hemophilia b. Synonyms: Idelvion; rIX-RFP. | |
| ALC-0159 | Cas No. 1849616-42-7. | |
| ALC-0159 | ALC-0159, a polyethylene glycol (PEG) lipid conjugate, could be used as vaccine excipient [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 1849616-42-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-138300. |  |
| ALC-0159 | ALC-0159 is a PEG/lipid conjugate (i.e. PEGylated lipid), specifically, it is the N,N-dimyristylamide of 2-hydroxyacetic acid, O-pegylated to a PEG chain mass of about 2 kilodaltons (corresponding to about 45-46 ethylene oxide units per molecule of N,N-dimyristyl hydroxyacetamide). It is a non-ionic surfactant by its nature. It has been deployed in the Pfizer-BioNTech SARS-CoV-2 mRNA vaccine that contains the active ingredient tozinameran. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ALC-0159; ALC 0159; ALC0159. Product Category: Others. Appearance: Solid. CAS No. 1849616-42-7. Molecular formula: (C2H4O)nC31H63NO2. Mole weight: 2450. Purity: >95%. IUPACName: 2-[(polyethylene glycol)-2000]-N,N-ditetradecylacetamide. Canonical SMILES: CCCCCCCCCCCCCCN(CCCCCCCCCCCCCC)C(COCCOC)=O. Product ID: ACM1849616427-1. Alfa Chemistry ISO 9001:2015 Certified. |  |
| ALC-0315 | ALC-0315 is a synthetic cationic lipid (or ionizable lipid). It is a colorless oily material, It has attracted attention as a component of the SARS-CoV-2 vaccine, BNT162b2, from BioNTech and Pfizer. Specifically, it is one of four components that form lipid nanoparticles (LNPs), which encapsulate and protect the otherwise fragile mRNA that is the active ingredient in these drugs. These nanoparticles promote the uptake of therapeutically effective nucleic acids such as oligonucleotides or mRNA both in vitro and in vivo. At physiological pH, ALC-0315 becomes protonated at the nitrogen atom, yielding an ammonium cation that is attracted to the messenger RNA (mRNA), which is anionic. (https://en.wikipedia.org/wiki/ALC-0315). Uses: Designed for use in research and industrial production. Additional or Alternative Names: ALC-0315; ALC 0315; ALC0315. Product Category: Others. Appearance: Colorless to light yellow oily liquid. CAS No. 2036272-55-4. Molecular formula: C48H95NO5. Mole weight: 766.29. Purity: >98%. IUPACName: [(4-Hydroxybutyl)azanediyl]di(hexane-6,1-diyl) bis(2-hexyldecanoate). Canonical SMILES: OCCCCN(CCCCCCOC(C(CCCCCC)CCCCCCCC)=O)CCCCCCOC(C(CCCCCC)CCCCCCCC)=O. Product ID: ACM2036272554-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| ALC-0315 | ALC-0315 is an ionisable aminolipid that is responsible for mRNA compaction and aids mRNA cellular delivery and its cytoplasmic release through suspected endosomal destabilization. ALC-0315 can be used to form lipid nanoparticle (LNP) delivery vehicles. Lipid-Nanoparticles have been used in the research of mRNA COVID-19 vaccine [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 2036272-55-4. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-138170. | |
| ALC-0315 | Cas No. 2036272-55-4. | |
| Alcaftadine | Alcaftadine (R89674) is a histamine H1 receptor antagonist, which is used to prevent eye irritation brought on by allergic conjunctivitis. Alcaftadine is a broad-spectrum antihistamine displaying a high affinity for histamine H1 and H2 receptors and a lower affinity for H4 receptors. Alcaftadine also exhibits modulatory action on immune cell recruitment and mast cell stabilizing effects [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R89674. CAS No. 147084-10-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17039. | |
| Alcaftadine | Alcaftadine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 11-(1-methylpiperidin-4-ylidene)-5,6-dihydroimidazo[2,1-b][3]benzazepine-3-carbaldehyde; UNII-7Z8O94ECSX; alcaftadinum; Vilasta; Lastacaft; Alcaftadine; alcaftadina. CAS No. 147084-10-4. Molecular formula: C19H21N3O. Mole weight: 307.39. Purity: 99%+. IUPACName: 11-(1-methylpiperidin-4-ylidene)-5,6-dihydroimidazo[2,1-b][3]benzazepine-3-carbaldehyde. Canonical SMILES: CN1CCC(=C2C3=CC=CC=C3CCN4C2=NC=C4C=O)CC1. Product ID: ACM147084104. Alfa Chemistry ISO 9001:2015 Certified. | |
| Alcaftadine | Alcaftadine(R89674) is a H1 histamine receptor antagonist, which is used to prevent eye irritation brought on by allergic conjunctivitis. Uses: Histamine h1 antagonists. Synonyms: Lastacaft. Grades: 0.98. CAS No. 147084-10-4. Molecular formula: C19H21N3O. Mole weight: 307.397. | |
| Alcaftadine | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Alcaftadine 3-Carboxylic Acid | An analogue of Alcaftadine. Synonyms: 6,11-Dihydro-11-(1-methyl-4-piperidinylidene)-5H-Imidazo[2,1-b][3]benzazepine-3-carboxylic Acid. Grades: > 95%. CAS No. 147083-93-0. Molecular formula: C19H21N3O2. Mole weight: 323.4. | |
| Alcaftadine N-Oxide | An analogue of Alcaftadine. Synonyms: 6,11-Dihydro-11-(1-methyl-1-oxido-4-piperidinylidene)-5H-imidazo[2,1-b][3]benzazepine-3-carboxaldehyde. Grades: > 95%. CAS No. 952649-75-1. Molecular formula: C19H21N3O2. Mole weight: 323.4. | |
| Alcesefoliside | Alcesefoliside. Group: Biochemicals. CAS No. 124151-38-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Alcian blue 8gx | Alcian blue 8gx. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ALCIAN(TM) BLUE 8GX;ALCIAN BLUE;ALCIAN BLUE 8 GS;CI NO 74240;CI 74240;INGRAIN BLUE;INGRAIN BLUE I;PROPOXYLATED ASTRA BLUE. Product Category: Heterocyclic Organic Compound. CAS No. 12633-95-3. Molecular formula: C56H68Cl4CuN16S4. Mole weight: 1298.86. Purity: 0.96. IUPACName: ALCIAN BLUE 8GX. Product ID: ACM12633953. Alfa Chemistry ISO 9001:2015 Certified. | |
| Alcian Blue 8GX | Alcian Blue 8GX is a commonly used phthalocyanine dye that binds to glycoproteins and glycosaminoglycans. Alcian Blue 8GX has a wide range of applications in biological staining, including proteins in brain tumors and DNA in cells and tissues [1] [2] [3] [4]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 33864-99-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-D0001. | |
| Alcian blue 8GX Certified | Alcian blue 8GX Certified. Group: Biochemicals. Alternative Names: Ingrain blue 1; CI 7424. Grades: Highly Purified. CAS No. 33864-99-2. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C56H68N16S4Cl4Cu. US Biological Life Sciences. | Worldwide |
| Alcian Blue 8GX, Certified ~50% (Dye content) | Alcian Blue 8GX, Certified ~50% (Dye content). Group: Biochemicals. Grades: Certified Dye. Pack Sizes: 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Alcian Blue 8GX (C.I. 74240) | 10g Pack Size. Group: Stains & Indicators. Formula: C56H68Cl4CuN16S4. CAS No. 33864-99-2. Prepack ID 59508864-10g. Molecular Weight 1298.86. See USA prepack pricing. |  |
| Alcian Yellow | Alcian Yellow. Group: Biochemicals. Alternative Names: [Di methyl amino- [ [2- [4- [4- [5- [ (di methyl aminodi methyl azaniumylidene methyl ) sulfanyl methyl ] -6- methyl -1, 3-benzothiazol-2-yl] phenyl] diazenylphenyl] -6- methyl -1, 3-benzothiazol-5-yl] methyl sulfanyl] methyl idene] di methyl azanium chloride. Grades: Highly Purified. CAS No. 61968-76-1. Pack Sizes: 2g, 5g, 10g, 25g, 50g. Molecular Formula: C40H46Cl2N8S4. US Biological Life Sciences. | Worldwide |
| Alcian Yellow (C.I. 12840) | 1g Pack Size. Group: Stains & Indicators. Formula: C40H46Cl2N8S4. CAS No. 61968-76-1. Prepack ID 30097302-1g. Molecular Weight 838.02. See USA prepack pricing. | |
| Alcian Yellow ≥87% | Alcian Yellow ≥87%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g. US Biological Life Sciences. | Worldwide |
| Alcindoromycin | It is produced by the strain of Actinosporangium sp. C36145. It has anti-gram-positive bacteria and anti-tumor effect. Synonyms: 1-Naphthacenecarboxylic acid, 1,2,3,4,6,11-hexahydro-4-((O-2,6-dideoxy-alpha-L-lyxo-hexopyranosyl-(1-4)-O-2,6-dideoxy-alpha-L-lyxo-hexopyranosyl-(1-4)-2,3,6-trideoxy-3-(methylamino)-alpha-L-lyxo-hexopyranosyl)oxy)-6,11-dioxo-2-ethyl-2,5,7,10-tetrahydroxy-, methyl ester, (1R-(1-alpha,2-beta,4-beta))-; DTXSID10993434; NSC304415; NSC-304415. Grades: 98%. CAS No. 72586-21-1. Molecular formula: C41H53NO17. Mole weight: 831.85. | |
| Alclofenac | Analgesic; antipyretic; anti-inflammatory. Group: Biochemicals. Alternative Names: 3-Chloro-4-(2-propen-1-yloxy)benzeneacetic Acid; [4-(Allyloxy)-3-chlorophenyl]acetic Acid; [3-Chloro-4- (allyloxy) phenyl]acetic Acid; Aclofenac; Allopydin; Epinal; MY 101; Medifenac; Mervan; Neosten; Neoston; Prinalgin; Reufenac; W 7320; Zumaril. Grades: Highly Purified. CAS No. 22131-79-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Alclometasone 17,21-Dipropionate | Alclometasone 17,21-Dipropionate. Group: Biochemicals. Alternative Names: Aclovate; Alclometasone dipropionate; Almeta; Delonal; Sch 22219; Vaderm; (7α,11 β,16α)-7-Chloro-11-hydroxy-16-methyl-17,21-bis(1-oxopropoxy)pregna-1,4-diene-3,20-dione. Grades: Highly Purified. CAS No. 66734-13-2. Pack Sizes: 2.5mg. Molecular Formula: C28H37ClO7, Molecular Weight: 521.04. US Biological Life Sciences. | Worldwide |
| Alclometasone dipropionate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Alclometasone dipropionate | Alclometasone dipropionate (Sch 22219) is a steroid compound. Alclometasone dipropionate can be used for the research of dermatitis and skin itch [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sch 22219. CAS No. 66734-13-2. Pack Sizes: 2.5 mg. Product ID: HY-106566. | |
| Alclometasone Dipropionate | Alclomethasone-17,21-dipropionate is the dipropionate salt form of alclometasone, which is a synthetic corticosteroid with low to medium potency. It is used in dermatology as an anti-inflammatory, antiallergic, antipruritic, vasoconstrictive and antiproliferative agent. It is also used for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. It was developed by Fougera Pharmaceuticals and has been listed. Uses: Alclomethasone-17,21-dipropionate is used in dermatology as an anti-inflammatory, antiallergic, antipruritic, vasoconstrictive and antiproliferative agent. it is also used for the relief of the inflammatory and pruritic manifestations of corticosteroid-re. Synonyms: Delonal; Vaderm; Aclosone; Alclomethasone-17,21-dipropionate; (7alpha,11beta,16alpha)-7-Chloro-11-hydroxy-16-methyl-17,21-bis(1-oxopropoxy)pregna-1,4-diene-3,20-dione. Grades: 95%. CAS No. 66734-13-2. Molecular formula: C28H37ClO7. Mole weight: 521.05. | |
| Alclometasone Dipropionate Impurity 1 | An Impurity of Alclometasone Dipropionate. Synonyms: 11β,17,21-Trihydroxy-16α-methylpregna-1,4-diene-3,20-dione 17,21-Dipropionate. Grades: > 95%. CAS No. 71868-53-6. Molecular formula: C28H38O7. Mole weight: 486.61. | |
| Alclometasone dipropionate Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Alcohol C-10 | Alcohol C-10 (Decyl Alcohol). CAS No. 112-30-1. FEMA No. 2365. VIGON Item # 501059. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Alcohol C-11 Undecylenic | Alcohol C-11 Undecylenic. CAS No. 112-43-6. Kosher: Y. VIGON Item # 500551. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Alcohol C-12 Lauric FCC | Alcohol C-12 Lauric FCC (Dodecanol). CAS No. 112-53-8. FEMA No. 2617. VIGON Item # 500501. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Alcohol C-13 Oxo | Alcohol C-13 Oxo. CAS No. 68526-86-3. VIGON Item # 501690. Categories: Speciality Ingredients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Alcohol C-6 FCC | Alcohol C-6 FCC (Hexyl Alcohol). CAS No. 111-27-3. FEMA No. 2567. VIGON Item # 500548. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Alcohol C-7 | Alcohol C-7 (Heptanol). CAS No. 111-70-6. FEMA No. 2548. Kosher: Y. VIGON Item # 501132. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Alcohol C-8 FCC | Alcohol C-8 FCC (Octyl Alcohol). CAS No. 111-87-5. FEMA No. 2800. VIGON Item # 500547. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Alcohol C-9 FCC | Alcohol C-9 FCC (Nonyl Alcohol). CAS No. 143-08-8. FEMA No. 2789. Kosher: Y. VIGON Item # 500561. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| 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 (azurin) | A soluble, periplasmic PQQ-containing quinohemoprotein. Also contains a single heme c. Occurs in Comamonas and Pseudomonas. Does not require an amine activator. Oxidizes a wide range of primary and secondary alcohols, and also aldehydes and large substrates such as sterols; methanol is not a substrate. Usually assayed with phenazine methosulfate or ferricyanide. Like all other quinoprotein alcohol dehydrogenases it has an 8-bladed propeller structure, a calcium ion bound to the PQQ in the active site and an unusual disulfide ring structure in close proximity to the PQQ. Group: Enzymes. Synonyms: type II quinoprotein alcohol dehydrogenase; quinohaemoprotein ethanol dehydrogenase; QHEDH; ADHIIB. Enzyme Commission Number: EC 1.1.9.1. 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-0438; alcohol dehydrogenase (azurin); EC 1.1.9.1; type II quinoprotein alcohol dehydrogenase; quinohaemoprotein ethanol dehydrogenase; QHEDH; ADHIIB. Cat No: EXWM-0438. | |
| Alcohol Dehydrogenase (Crude Enzyme) | This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Synthesis; medicine. Group: Enzymes. Synonyms: aldehyde reductase (NADPH2); NADP-alcohol dehydrogenase; NADP + -aldehyde reductase; NADP + -dependent aldehyde reductase; NADPH-aldehyde reductase; NADPH-dependent aldehyde reductase; nonspecific succinic semialdehyde reductase; ALR 1; low-Km aldehyde reductase; high-Km aldehyde reductase; alcohol dehydrogenase (NADP). Enzyme Commission Number: EC 1.1.1.2. CAS No. 9028-12-0. ALR. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. aldehyde reductase (NADPH2); NADP-alcohol dehydrogenase; NADP + -aldehyde reductase; NADP + -dependent aldehyde reductase; NADPH-aldehyde reductase; NADPH-dependent aldehyde reductase; nonspecific succinic semialdehyde reductase; ALR 1; low-Km aldehyde reductase; high-Km aldehyde reductase; alcohol dehydrogenase (NADP). Pack: 100ml. Cat No: NATE-1792. | |
| alcohol dehydrogenase (cytochrome c) | A periplasmic PQQ-containing quinoprotein. Occurs in Pseudomonas and Rhodopseudomonas. The enzyme from Pseudomonas aeruginosa uses a specific inducible cytochrome c550 as electron acceptor. Acts on a wide range of primary and secondary alcohols, but not methanol. It has a homodimeric structure [contrasting with the heterotetrameric structure of EC 1.1.2.7, methanol dehydrogenase (cytochrome c)]. It is routinely assayed with phenazine methosulfate as electron acceptor. Activity is stimulated by ammonia or amines. Like all other quinoprotein alcohol dehydrogenases it has an 8-bladed 'propeller' structure, a calcium ion bound to the PQQ in the active site and an unusual disulfide ring structure in close proximity to the PQQ. Group: Enzymes. Synonyms: type I quinoprotein alcohol dehydrogenase; quinoprotein ethanol dehydrogenase. Enzyme Commission Number: EC 1.1.2.8. 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-0390; alcohol dehydrogenase (cytochrome c); EC 1.1.2.8; type I quinoprotein alcohol dehydrogenase; quinoprotein ethanol dehydrogenase. Cat No: EXWM-0390. | |
| Alcohol Dehydrogenase equine | recombinant, expressed in E. coli, ?0.5 U/mg. Group: Fluorescence/luminescence spectroscopy. | |
| 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 (NADP+) | A zinc protein. Some members of this group oxidize only primary alcohols; others act also on secondary alcohols. May be identical with EC 1.1.1.19 (L-glucuronate reductase), EC 1.1.1.33 [mevaldate reductase (NADPH)] and EC 1.1.1.55 [lactaldehyde reductase (NADPH)]. Re-specific with respect to NADPH. Group: Enzymes. Synonyms: aldehyde reductase (NADPH2); NADP-alcohol dehydrogenase; NADP+-aldehyde reductase; NADP+-dependent aldehyde reductase; NADPH-aldehyde reductase; NADPH-dependent aldehyde reductase; nonspecific succinic semialdehyde reductase; ALR 1; low-Km aldehyde reductase; high-Km aldehyde reductase; alcohol dehydrogenase (NADP). Enzyme Commission Number: EC 1.1.1.2. CAS No. 9028-12-0. ALR. 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-0103; alcohol dehydrogenase (NADP+); EC 1.1.1.2; 9028-12-0; aldehyde reductase (NADPH2); NADP-alcohol dehydrogenase; NADP+-aldehyde reductase; NADP+-dependent aldehyde reductase; NADPH-aldehyde reductase; NADPH-dependent aldehyde reductase; nonspecific succinic semialdehyde reductase; ALR 1; low-Km aldehyde reductase; high-Km aldehyde reductase; alcohol dehydrogenase (NADP). Cat No: EXWM-0103. | |
| 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 Dehydrogenase (NADP+ dependent) from E. coli, Recombinant | Alcohol dehydrogenase [NADP+] also known as aldehyde reductase or aldo-keto reductase family 1 member A1 is an enzyme that in humans is encoded by the AKR1A1 gene. This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. This member, also known as aldehyde reductase, is involved in the reduction of biogenic and xenobiotic aldehydes and is present in virtually every tissue. Alternative splicing of this gene results in two transcript variants encoding the same protein. Group: Enzymes. Synonyms: EC 1.1.1.2; Aromatic Alcohol Dehydrogenase; Alcohol:NADP+ oxidoreductase; AKR1A1; ALDR1; ALR; . Enzyme Commission Number: EC 1.1.1.2. CAS No. 9028-12-0. ALR. Activity: >500 U/ml. Form: Liquid. Source: E. coli. Species: E. coli. EC 1.1.1.2; Aromatic Alcohol Dehydrogenase; Alcohol:NADP+ oxidoreductase; AKR1A1; ALDR1; ALR; ARM; DD3; HEL-S-6; aldehyde reductase; aldo-keto reductase family 1 member A1; alcohol dehydrogenase (NADP+); aldehyde reductase (NADPH2); NADP-alcohol dehydrogenase; NADP+-aldehyde reductase; NADP+-dependent aldehyde reductase; NADPH-aldehyde reductase; NADPH-dependent aldehyde reductase; nonspecific succinic semialdehyde reductase; ALR 1; low-Km aldehyde reductase; high-Km aldehyde reductase; alcohol dehydrogenase (NADP). Cat No: NATE-1589. | |
| Alcohol Dehydrogenase (NADP+ dependent) from Entamoeba species, Recombinant | NADP-dependent isopropanol dehydrogenase belongs to the superfamily of alcohol dehydrogenases with a preference for medium chain secondary alcohols, such as 2- butanol and isopropanol, while it has low activity with primary alcohols, such as ethanol. Under physiological conditions, the enzyme reduces aldehydes and 2-ketones to produce secondary alcohols. It is also active with acetaldehyde and propionaldehyde. Group: Enzymes. Synonyms: EC 1.1.1.2; Aromatic Alcohol Dehy. Purity: > 95% by SDS-PAGE. ALR. Mole weight: ~40.9 kDa (SDS-PAGE). Activity: > 60U/mg. Storage: Aliquot and store at -20°C. Avoid repeated freeze thaw cycles. Form: Liquid, 1 mg/mL solution in 50 mM Tris-HCl buffer (pH 8.0) containing 100 mM NaCl and 50% glycerol. Source: E. coli. Species: Entamoeba species. EC 1.1.1.2; Aromatic Alcohol Dehydrogenase; Alcohol:NADP+ oxidoreductase; AKR1A1; ALDR1; ALR; ARM; DD3; HEL-S-6; aldehyde reductase; aldo-keto reductase family 1 member A1; alcohol dehydrogenase (NADP+); aldehyde reductase (NADPH2); NADP-alcohol dehydrogenase; NADP+-aldehyde reductase; NADP+-dependent aldehyde reductase; NADPH-aldehyde reductase; NADPH-dependent aldehyde reductase; nonspecific succinic semialdehyde reductase; ALR 1; low-Km aldehyde reductase; high-Km aldehyde reductase; alcohol dehydrogenase (NADP). Cat No: NATE-1590. | |
| alcohol dehydrogenase (nicotinoprotein) | Contains Zn2+. Nicotinoprotein alcohol dehydrogenases are unique medium-chain dehydrogenases/reductases (MDR) alcohol dehydrogenases that have a tightly bound NAD+/NADH cofactor that does not dissociate during the catalytic process. Instead, the cofactor is regenerated by a second substrate or electron carrier. While the in vivo electron acceptor is not known, N,N-dimethyl-4-nitrosoaniline (NDMA), which is reduced to 4-(hydroxylamino)-N,N-dimethylaniline, can serve this function in vitro.The enzyme from the Gram-positive bacterium Amycolatopsis methanolica can accept many primary alcohols as substrates, including benzylalcohol. Group: Enzymes. Synonyms: NDMA-dependent alcohol dehydrogenase; nicotinoprotein alcohol dehydrogenase; np-ADH; ethanol:N,N-dimethyl-4-nitrosoaniline oxidoreductase. Enzyme Commission Number: EC 1.1.99.36. 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-0464; alcohol dehydrogenase (nicotinoprotein); EC 1.1.99.36; NDMA-dependent alcohol dehydrogenase; nicotinoprotein alcohol dehydrogenase; np-ADH; ethanol:N,N-dimethyl-4-nitrosoaniline oxidoreductase. Cat No: EXWM-0464. | |
| alcohol dehydrogenase (quinone) | Only described in acetic acid bacteria where it is involved in acetic acid production. Associated with membrane. Electron acceptor is membrane ubiquinone. A model structure suggests that, like all other quinoprotein alcohol dehydrogenases, the catalytic subunit has an 8-bladed propeller structure, a calcium ion bound to the PQQ in the active site and an unusual disulfide ring structure in close proximity to the PQQ; the catalytic subunit also has a heme c in the C-terminal domain. The enzyme has two additional subunits, one of which contains three molecules of heme c. It does not require amines for activation. It has a restricted substrate specificity, oxidizing a few primary alcohols (C2 to C6), but not methanol, secondary alcohols and some aldehydes. It is assayed with phenazine methosulfate or with ferricyanide. Group: Enzymes. Synonyms: type III ADH; membrane associated quinohaemoprotein alcohol dehydrogenase. Enzyme Commission Number: EC 1.1.5.5. 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-0433; alcohol dehydrogenase (quinone); EC 1.1.5.5; type III ADH; membrane associated quinohaemoprotein alcohol dehydrogenase. Cat No: EXWM-0433. | |
| Alcohol Dehydrogenase, recombinant from E. coli | ?500 U/mL. Group: Fluorescence/luminescence spectroscopy. | |
| Alcohol dehydrogenase, Saccharomyces cerevisiae | Alcohol dehydrogenase, Saccharomyces cerevisiae is a dimeric protein in the cytosol of cells. Alcohol dehydrogenase, the key enzyme for alcohol consumption in the body, is the highest expressed in the liver and participates in the detoxification mechanism of environmental alcohol [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EC 1.1.1.1. CAS No. 9031-72-5. Pack Sizes: 25 KU. Product ID: HY-P2740. | |
| Alcohol, Denatured, Reagent, ACS | Alcohol, Denatured, Reagent, ACS. Grades: ACS. CAS No. 64-17-5. Product ID: 8-04899. Molecular formula: C2H5OH. Mole weight: 46.07. |  |
| alcohol-forming fatty acyl-CoA reductase | The enzyme has been characterized from the plant Simmondsia chinensis (jojoba). The alcohol is formed by a four-electron reduction of fatty acyl-CoA. Although the reaction proceeds through an aldehyde intermediate, a free aldehyde is not released. The recombinant enzyme was shown to accept saturated and mono-unsaturated fatty acyl-CoAs of 16 to 22 carbons. Group: Enzymes. Synonyms: FAR (gene name); long-chain acyl-CoA:NADPH reductase. Enzyme Commission Number: EC 1.2.1.84. 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-1187; alcohol-forming fatty acyl-CoA reductase; EC 1.2.1.84; FAR (gene name); long-chain acyl-CoA:NADPH reductase. Cat No: EXWM-1187. | |
| 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 O-cinnamoyltransferase | Acceptor alcohols (ROH) include methanol, ethanol and propanol. No cofactors are required as 1-O-trans-cinnamoyl-β-D-glucopyranose itself is an "energy-rich" (activated) acyl-donor, comparable to CoA-thioesters. 1-O-trans-Cinnamoyl-β-D-gentobiose can also act as the acyl donor, but with much less affinity. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.152. CAS No. 203009-15-8. 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-2092; alcohol O-cinnamoyltransferase; EC 2.3.1.152; 203009-15-8. Cat No: EXWM-2092. | |
| alcohol oxidase | The enzymes from the fungi Candida methanosorbosa and several Basidiomycetes species contain an FAD cofactor. The enzyme from the phytopathogenic fungi Colletotrichum graminicola and Colletotrichum gloeosporioides utilize a mononuclear copper-radical mechanism. The enzyme acts on primary alcohols and unsaturated alcohols, and has much lower activity with branched-chain and secondary alcohols. Group: Enzymes. Synonyms: ethanol oxidase; alcohol:oxygen oxidoreductase. Enzyme Commission Number: EC 1.1.3.13. CAS No. 9073-63-6. Alcohol Oxidase. 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-0395; alcohol oxidase; EC 1.1.3.13; 9073-63-6; ethanol oxidase; alcohol:oxygen oxidoreductase. Cat No: EXWM-0395. | |
| Alcohol oxidase | Alcohol oxidase is a functional enzyme of methanol utilization pathway and can be isolated from yeast peroxisome [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AO; AOX. CAS No. 9073-63-6. Pack Sizes: 50 U; 250 U. Product ID: HY-P2756. | |
| Alcohols, C10-14, ethoxylated | Alcohols, C10-14, ethoxylated. Uses: Designed for use in research and industrial production. CAS No. 66455-15-0. Purity: 0.96. Product ID: ACM66455150. Alfa Chemistry ISO 9001:2015 Certified. | |
| Alcohols,C11-15-secondary, ethoxylated | Synonyms: DETERGENT BIOGRAD FL-70; TERGITOL TYPE NP-9; TERGITOL TYPE NP-10; TERGITOL TYPE NP-7; TERGITOL TYPE 15-S-12; TERGITOL TYPE 15-S-30; TERGITOL TYPE 15-S-5; TERGITOL TYPE 15-S-7. CAS No. 68131-40-8. Molecular formula: C11-15H23-31O(CH2CCH2O)xH. | |
| Alcohols,C12-13, ethoxylated | Grades: 95%. CAS No. 66455-14-9. | |
| Alcohols,C12-15, ethoxylated propoxylated | Grades: 95%. CAS No. 68551-13-3. | |
| Alcohols, C14-18 and C18-unsatd., branched and linear | Alcohols, C14-18 and C18-unsatd., branched and linear. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Alcohols, C14-18 and C18-unsatd., branched and linear;ISOOLEYL ALCOHOL;Einecs 288-286-5. Product Category: Heterocyclic Organic Compound. CAS No. 85711-27-9. Product ID: ACM85711279. Alfa Chemistry ISO 9001:2015 Certified. | |
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