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| Product | Description | |
|---|---|---|
| Cholesterol-d7 | Cholesterol-d 7 is the deuterium labeled Cholesterol. Cholesterol is the major sterol in mammals. It is making up 20-25% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins [1] [2]. Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist [3]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 83199-47-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N0322S. |  |
| Cholesterol-d7 | Cholesterol-d7. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CHOLESTEROL-25,26,26,26,27,27,27-D7;(3)-Cholest-5-en-3-ol-d7;Cholesterol-d7. Product Category: Heterocyclic Organic Compound. Appearance: White to Off-White Solid. CAS No. 83199-47-7. Molecular formula: C27H39D7O. Mole weight: 393.7. Purity: 99 atom % D. Product ID: ACM83199477. Alfa Chemistry ISO 9001:2015 Certified. Categories: Cholesterol-dependent cytolysin. |  |
| Cholesterol-d7 Tetrahydropyranyl Ether | Cholesterol Tetrahydropyranyl Ether is a Cholesterol (C432501) derivative used in the preparation of ginsenoside Rk1 cholesterol analogs and 7α- and 7 β-aminocholestanol derivatives. Group: Biochemicals. Alternative Names: 2-[[(3 β)-Cholest-5-en-3-yl]oxy]tetrahydro-2H-pyran-d7; Cholesterol-d7 Tetrahydropyran-2-yl Ether; Cholesteryl-d7 Tetrahydropyranyl Ether; Tetrahydropyranyl Cholesterol-d7. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Cholesterol Dehydrogenase from Nocardia sp. | Cholesterol dehydrogenase is an enzyme that uses nicotinamide adenine dinucleotide/nicotinamide adenine dinucleotide phosphate (NAD(P)) as its cofactor in oxidizing cholesterol to form cholest-4-en-3-one. This enzyme oxidizes the hydroxyl group at the 3 position of the sterol ring to form a ketone. Group: Enzymes. Synonyms: Cholesterol Dehydrogenase; CDH. CAS No. 67775-34-2. Activity: 10U/mg-solid or more. Storage: at -20°C. Form: Freeze dried powder. Source: Nocardia sp. Cholesterol Dehydrogenase; CDH. Cat No: NATE-0892. |  |
| Cholesterol ?-D-glucoside | ?97% (TLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Cholesterol Esterase from Candida Rugosa | Cholesterol esterase (CE) is also known as cholesterol ester hydrolase. This enzyme catalyzes the following reaction: Sterol Ester --------> Sterol + Fatty Acid. Cholesterol esterase activity has been demonstrated in pancreas, intestine, liver and kidney. The enzyme is inactivated by proteolytic enzymes but stabilized by proteolytic enzyme inhibitors and by bile salts. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; sterol esterase; CE. Enzyme Commission Number: EC 3.1.1.13. CAS No. 9026-00-0. Purity: 0.9. Activity: 25-100 U/mg. Storage: Store at -20° C. Form: Freeze dried powder. Source: Candida Rugosa. cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; sterol esterase; CE. Cat No: NATE-1679. | |
| Cholesterol Esterase from E. coli, Recombinant | Sterol esterase belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. The systematic name of this enzyme class is steryl-ester acylhydrolase. This enzyme participates in bile acid biosynthesis. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Enzyme Commission Number: EC 3.1.1.13. CAS No. 9026-00-0. Cholesterol Esterase. Mole weight: ca. 54 kDa. Activity: > 5 U/mg lyophilizate. Appearance: Light yellow lyophilizate. Source: E. coli. Species: E. coli. cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Cat No: DIA-405. | |
| Cholesterol Esterase from Microorganism | Cholesterol esterase (CE) is also known as cholesterol ester hydrolase. This enzyme catalyzes the following reaction: Sterol Ester --------> Sterol + Fatty Acid. Cholesterol esterase activity has been demonstrated in pancreas, intestine, liver and kidney. The enzyme is inactivated by proteolytic enzymes but stabilized by proteolytic enzyme inhibitors and by bile salts. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Enzyme Commission Number: EC 3.1.1.13. CAS No. 9026-00-0. Activity: 5.0U/mg-solid or more. Form: Freeze dried powder. Source: Microorganism. cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Cat No: DIA-135. | |
| Cholesterol Esterase from porcine pancreas | lyophilized, powder, white, ~35 U/mg. Group: Fluorescence/luminescence spectroscopy. | |
| Cholesterol Esterase from Pseudomonas sp. | Cholesterol esterase (CE) is also known as cholesterol ester hydrolase. This enzyme catalyzes the following reaction: Sterol Ester --------> Sterol + Fatty Acid. Cholesterol esterase activity has been demonstrated in pancreas, intestine, liver and kidney. The enzyme is inactivated by proteolytic enzymes but stabilized by proteolytic enzyme inhibitors and by bile salts. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Enzyme Commission Number: EC 3.1.1.13. CAS No. 9026-00-0. Activity: 100U/mg-solid or more (containing approx. 40% of stabilizers). Form: Freeze dried powder. Source: Pseudomonas sp. cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Cat No: DIA-134. | |
| Cholesterol Esterase from Schizophyllum commune | Cholesterol esterase (CE) is also known as cholesterol ester hydrolase. This enzyme catalyzes the following reaction: Sterol Ester --------> Sterol + Fatty Acid. Cholesterol esterase activity has been demonstrated in pancreas, intestine, liver and kidney. The enzyme is inactivated by proteolytic enzymes but stabilized by proteolytic enzyme inhibitors and by bile salts. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Enzyme Commission Number: EC 3.1.1.13. CAS No. 9026-00-0. Activity: 2.0 U/mg-solid or more (containing approx. 20% of stabilizers). Form: Freeze dried powder. Source: Schizophyllum commune. cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Cat No: DIA-133. | |
| Cholesterol Esterase, PEG Modified | PEG (Polyethylene glycol) modified cholesterol esterase (PEG Cholesterol Esterase) isone of our premier cholesterol esterase conjugates. Cholesterol esterase is an enzyme that catalyzes the hydrolysis of cholesterol esters into their sterol components and fatty acids. Cholesterol esterase has clinical applications in the determination of serum cholesterol combined with other enzymes. PEG modified cholesterol esterase shows better stability with good reactivity. All our labeled cholesterol esterase products were performed under mild reaction conditions to retain their maximum bioactivity. These conjugates were further purified by chromatography to ensure adequate applications both in-vitro and in-vivo. Conjugate ration: 20~50 peg5000/monomer. solubility: soluble in aqueous buffer. Group: Enzymes. Synonyms: PEG Cholesterol Esterase; Cholesterol Esterase-polyethylene glycol; CE-polyethylene glycol; CE-PEG; PEG-CE; PEG-Cholesterol Esterase. Cholesterol Esterase. Mole weight: ~65 kD for monomer; 400 kD for hexamer. Activity: >300 units/g. Storage: Store at -20°C. Form: Lyophilized powder. Source: Porcine pancreas. Species: Porcine. PEG Cholesterol Esterase; Cholesterol Esterase-polyethylene glycol; CE-polyethylene glycol; CE-PEG; PEG-CE; PEG-Cholesterol Esterase; Cholesterol Esterase, PEG Modified. Cat No: NATE-1587. | |
| Cholesterol esterase, Pseudomonas | Cholesterol esterase, Pseudomonas is an enzyme that hydrolyzes cholesterol ester to cholesterol and free fatty acid in the intestinal lumen. Cholesterol synthesized in the acinar cells and is stored in zymogen granules. Cholesterol esterase is also known as bile salt-stimulated lipase and carboxy ester lipasea, acts function for acceleration of cholesterol absorption [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9026-00-0. Pack Sizes: 100 U. Product ID: HY-P2879. | |
| Cholesterol formate | Cholesterol formate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CHOLESTEROL FORMATE; 5-CHOLESTEN-3BETA-OL 3-FORMATE; Cholest-5-en-3beta-yl formate; Cholest-5-en-3-ol (3beta)-,formate; Cholesterol Formate; FORMIC ACID CHOLESTEROL ESTER; Cholest-5-en-3-yl formate. Product Category: Steroidal Compounds. CAS No. 4351-55-7. Molecular formula: C28H46O2. Mole weight: 414.66. Purity: 0.96. IUPACName: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]formate. Canonical SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC=O)C)C. Density: 1g/cm³. ECNumber: 224-416-9. Product ID: ACM4351557. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholesterol heptanoate | Cholesterol heptanoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Heptanoic Acid Cholesterol Ester. Product Category: Steroidal CompoundsCholesteryl Esters. Appearance: Powder to crystal. CAS No. 1182-07-6. Molecular formula: C34H58O2. Mole weight: 498.8. Purity: 99%+. IUPACName: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] heptanoate. Canonical SMILES: CCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCCC(C)C)C)C. Density: 0.97g/cm³. ECNumber: 214-654-1. Product ID: ACM1182076. Alfa Chemistry ISO 9001:2015 Certified. Categories: Cholesteryl heptanoate. | |
| Cholesterol Heptyl Carbonate, GR | Cholesterol Heptyl Carbonate, GR. Group: Liquid crystal (lc) materials. CAS No. 15455-81-9. Product ID: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] heptyl carbonate. Molecular formula: 528.8g/mol. Mole weight: C35H60O3. CCCCCCCOC (=O)OC1CCC2 (C3CCC4 (C (C3CC=C2C1)CCC4C (C)CCCC (C)C)C)C. InChI=1S / C35H60O3 / c1-7-8-9-10-11-23-37-33 (36) 38-28-19-21-34 (5) 27 (24-28) 15-16-29-31-18-17-30 (26 (4) 14-12-13-25 (2) 3) 35 (31, 6) 22-20-32 (29) 34 / h15, 25-26, 28-32H, 7-14, 16-24H2, 1-6H3 / t26-, 28+, 29+, 30-, 31+, 32+, 34+, 35- / m1 / s1. VVEXXPUMMZEWSU-SJTWHRLHSA-N. |  |
| Cholesterol hydrogen phthalate | Cholesterol hydrogen phthalate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: NSC59691, EINECS 229-783-9, CID111235, Cholest-5-en-3beta-yl hydrogen phthalate, 6732-01-0. Product Category: Steroidal Compounds. CAS No. 6732-01-0. Molecular formula: C35H50O4. Mole weight: 534.77. Purity: 0.97. IUPACName: 2-[[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxycarbonyl]benzoic acid. Canonical SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C5=CC=CC=C5C(=O)O)C)C. Density: 1.11g/cm³. ECNumber: 229-783-9. Product ID: ACM6732010. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholesterol Impurity 14 | Cholesterol Impurity 14. Uses: For analytical and research use. Group: Impurity standards. CAS No. 15073-00-4. Molecular formula: C28H48O. Mole weight: 400.69. Catalog: APB15073004. | |
| Cholesterol isobutyl carbonate | Cholesterol isobutyl carbonate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Isobutyl Carbonic Acid Cholesterol Ester. Product Category: Heterocyclic Organic Compound. CAS No. 77546-35-1. Molecular formula: C32H54O3. Mole weight: 486.77. Purity: 0.96. IUPACName: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] 2-methylpropyl carbonate. Canonical SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)OCC(C)C)C)C. Product ID: ACM77546351. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholesterol methyl carbonate | Cholesterol methyl carbonate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CHOLESTERYL METHYL CARBONATE; CHOLESTEROL METHYL CARBONATE; Methyl Carbonic Acid Cholesterol Ester. Product Category: Steroidal Compounds. CAS No. 15507-52-5. Molecular formula: C29H48O3. Mole weight: 444.69. Purity: 0.95. IUPACName: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] methyl carbonate. Density: 1.02g/cm³. Product ID: ACM15507525. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholesterol methyl-ß-cyclodextrin complex | Cholesterol methyl-ß-cyclodextrin complex. Product ID: 4-00441. Purity: ~4w/w% cholesterol. |  |
| cholesterol monooxygenase (side-chain-cleaving) | A heme-thiolate protein (cytochrome P-450). The reaction proceeds in three stages, with two hydroxylations at C-22 and C-20 preceding scission of the side-chain between carbons 20 and 22. The initial source of the electrons is NADPH, which transfers the electrons to the adrenodoxin via EC 1.18.1.6, adrenodoxin-NADP+ reductase. Group: Enzymes. Synonyms: cholesterol desmolase; cytochrome P-450scc; C27-side chain cleavage enzyme; cholesterol 20-22-desmolase; cholesterol C20-22 desmolase; cholesterol side-chain cleavage enzyme; cholesterol side-chain-cleaving enzyme; steroid 20-22 desmolase; steroid 20-22-lyase; CYP11A1 (gene name). Enzyme Commission Number: EC 1.14.15.6. CAS No. 37292-81-2, 440354-98-3. 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-0949; cholesterol monooxygenase (side-chain-cleaving); EC 1.14.15.6; 37292-81-2, 440354-98-3; cholesterol desmolase; cytochrome P-450scc; C27-side chain cleavage enzyme; cholesterol 20-22-desmolase; cholesterol C20-22 desmolase; cholesterol side-chain cleavage enzyme; cholesterol side-chain-cleaving enzyme; steroid 20-22 desmolase; steroid 20-22-lyase; CYP11A1 (gene name). Cat No: EXWM-0949. | |
| Cholesterol myristate | Cholesterol myristate is a natural steroid present in traditional Chinese medicine. Cholesterol myristate binds to several ion channels such as the nicotinic acetylcholine receptor , GABAA receptor , and the inward-rectifier potassium ion channel. Uses: Scientific research. Group: Natural products. Alternative Names: Cholesteryl myristate; Cholesteryl tetradecanoate. CAS No. 1989-52-2. Pack Sizes: 500 mg; 1 g. Product ID: HY-N2338. | |
| Cholesterol N-amyl carbonate | Cholesterol N-amyl carbonate. Group: Liquid crystal (lc) materials. CAS No. 15455-79-5. Product ID: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] pentyl carbonate. Molecular formula: 500.8g/mol. Mole weight: C33H56O3. CCCCCOC (=O)OC1CCC2 (C3CCC4 (C (C3CC=C2C1)CCC4C (C)CCCC (C)C)C)C. InChI=1S/C33H56O3/c1-7-8-9-21-35-31 (34)36-26-17-19-32 (5)25 (22-26)13-14-27-29-16-15-28 (24 (4)12-10-11-23 (2)3)33 (29, 6)20-18-30 (27)32/h13, 23-24, 26-30H, 7-12, 14-22H2, 1-6H3/t24-, 26+, 27+, 28-, 29+, 30+, 32+, 33-/m1/s1. AXZGKUVSDXMPGA-FLFWOSPYSA-N. | |
| Cholesterol N-butyl carbonate | Cholesterol N-butyl carbonate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Cholesterol Butyl Carbonate, 41371-14-6, SureCN4426430, CTK8B1664, ANW-29618, Butyl Carbonic Acid Cholesterol Ester, AKOS015840352. Product Category: Heterocyclic Organic Compound. CAS No. 41371-14-6. Molecular formula: C32H54O3. Mole weight: 486.77. Purity: 0.96. IUPACName: butyl [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] carbonate. Canonical SMILES: CCCCOC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCCC(C)C)C)C. Product ID: ACM41371146. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholesterol NF | Cholesterol NF. CAS No. 57-88-5. Product ID: 8-04949. Molecular formula: C27H46O. Mole weight: 386.65. Properties: MFCD02684172. | |
| Cholesterol NF | Cholesterol NF. Grades: NF. CAS No. 57-88-5. Product ID: 8-01619. Molecular formula: C27H46O. Mole weight: 386.65. MFCD No. MFCD00003646. | |
| Cholesterol Nonyl Carbonate, ≥95% | Cholesterol Nonyl Carbonate, ≥95%. Group: Liquid crystal (lc) materials. CAS No. 15455-83-1. Product ID: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] nonyl carbonate. Molecular formula: 556.9g/mol. Mole weight: C37H64O3. CCCCCCCCCOC (=O)OC1CCC2 (C3CCC4 (C (C3CC=C2C1)CCC4C (C)CCCC (C)C)C)C. InChI=1S / C37H64O3 / c1-7-8-9-10-11-12-13-25-39-35 (38) 40-30-21-23-36 (5) 29 (26-30) 17-18-31-33-20-19-32 (28 (4) 16-14-15-27 (2) 3) 37 (33, 6) 24-22-34 (31) 36 / h17, 27-28, 30-34H, 7-16, 18-26H2, 1-6H3 / t28-, 30+, 31+, 32-, 33+, 34+, 36+, 37- / m1 / s1. CLVJSPXXNWCOJH-IATSNXCDSA-N. | |
| Cholesterol oleate methyl-ß-cyclodextrin complex | Cholesterol oleate methyl-ß-cyclodextrin complex. Product ID: 4-00446. Purity: ~2 w/w% cholesterol. | |
| Cholesterol Oleyl Carbonate, 70% | Cholesterol Oleyl Carbonate, 70%. Group: Liquid crystal (lc) materials. CAS No. 17110-51-9. Product ID: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] [(Z)-octadec-9-enyl] carbonate. Molecular formula: 681.1g/mol. Mole weight: C46H80O3. CCCCCCCCC=CCCCCCCCCOC (=O)OC1CCC2 (C3CCC4 (C (C3CC=C2C1)CCC4C (C)CCCC (C)C)C)C. InChI= 1S / C46H80O3 / c1-7-8-9-10-11-12-13-14-15-16-17-18-1 9-20-21-22-34-48-44 (47) 49-39-30-32-45 (5) 38 (35-39) 26-27-40-42-29-28-41 (37 (4) 25-23-24-36 (2) 3) 46 (42, 6) 33-31-43 (40) 45 / h14-15, 26, 36-37, 39-43H, 7-13, 16-25, 27-35H2, 1-6H3 / b15-14- / t37-, 39 + , 40 + , 41-, 42 + , 43 + , 45 + , 46- / m1 / s1. XMPIMLRYNVGZIA-TZOMHRFMSA-N. | |
| cholesterol oxidase | Contains FAD. Cholesterol oxidases are secreted bacterial bifunctional enzymes that catalyse the first two steps in the degradation of cholesterol. The enzyme catalyses the oxidation of the 3β-hydroxyl group to a keto group, and the isomerization of the double bond in the oxidized steroid ring system from the Δ5 position to Δ6 position (cf. EC 5.3.3.1, steroid Δ-isomerase). Group: Enzymes. Synonyms: cholesterol- O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase. Enzyme Commission Number: EC 1.1.3.6. CAS No. 9028-76-6. CHOD. 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-0424; cholesterol oxidase; EC 1.1.3.6; 9028-76-6; cholesterol- O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase. Cat No: EXWM-0424. | |
| Cholesterol oxidase | Cholesterol oxidase. Synonyms: EC 1.1.3.6;EC: 1.1.3.6;CHOLESTEROL OXIDASE;CHOLESTEROL OXIDASE MICROBIAL;CHOLESTEROL OXIDASE, NOCARDIA SPECIES;CHOLESTEROL: OXYGEN OXIDOREDUCTASE;CHOLESTEROL: OXYGEN OXIDOREDUCTASE MICROBIAL;cholesterol oxidase F. pseudomonas sp. CAS No. 9028-76-6. Product ID: CDF4-0046. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; Cholesterol oxidase; CDF4-0046; 9028-76-6; 232-842-1; 9028-76-6. Purity: 0.99. Color: Pale yellow. EC Number: 232-842-1. Physical State: Solution (Slightly hazy). Solubility: 50 mM potassium phosphate buffer, pH 7.0: soluble (Cold). Storage: -70°C. Product Description: Cholesterol Oxidase produced from Streptomyces sp corresponds to a molecular weight of 62 kDa. It has a pH and temperature optimum of 7 and 37 °C, respectively. Cholesterol Oxidase comprises a FAD-binding and a steroid-binding domain. |  |
| Cholesterol oxidase from E. coli, Recombinant | Recombinant Cholesterol Oxidase belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with oxygen as acceptor. This enzyme participates in bile acid biosynthesis. Group: Enzymes. Synonyms: EC 1.1.3.6, cholesterol-O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase; 9028-76-6. Enzyme Commission Number: EC 1.1.3.6. CAS No. 9028-76-6. CHOD. Mole weight: ca. 58 kDa. Activity: > 5 U/mg lyophilizate. Appearance: Yellow lyophilizate. Source: E. coli. Species: E. coli. EC 1.1.3.6, cholesterol-O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase; 9028-76-6. Cat No: DIA-406. | |
| Cholesterol oxidase from E. coli, Recombinant (liquid) | Recombinant Cholesterol Oxidase belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with oxygen as acceptor. This enzyme participates in bile acid biosynthesis. Group: Enzymes. Synonyms: EC 1.1.3.6, cholesterol-O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase; 9028-76-6. Enzyme Commission Number: EC 1.1.3.6. CAS No. 9028-76-6. CHOD. Mole weight: ca. 59 kDa. Activity: > 200 U/ml. Stability: stable at 25°C for at least one month. Form: Liquid form (30% sucrose solution). Source: E. coli. Species: E. coli. EC 1.1.3.6, cholesterol-O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase; 9028-76-6. Cat No: DIA-408. | |
| Cholesterol Oxidase from Microorganism | Cholesterol oxidase (CHOD) is a monomeric flavoprotein containing FAD that catalyzes the first step in cholesterol catabolism. This bifunctional enzyme oxidizes cholesterol to cholest-5-en-3-one in an FAD-requiring step, which is then isomerized to cholest-4-en-3-one with the release of H2O2. Group: Enzymes. Synonyms: Cholesterol-O2 oxidoreductase; 3 beta-Hydroxy steroid oxidoreductase; 3β-hydroxysteroid: oxygen oxidoreductase; cholesterol: oxygen oxidoreductase; cholesterol oxidase; EC 1.1.3.6. Enzyme Commission Number: EC 1.1.3.6. CAS No. 9028-76-6. Activity: 12U/mg-solid or more. Form: Freeze dried powder. Source: Microorganism. Cholesterol-O2 oxidoreductase; 3 beta-Hydroxy steroid oxidoreductase; 3β-hydroxysteroid: oxygen oxidoreductase; cholesterol: oxygen oxidoreductase; cholesterol oxidase; EC 1.1.3.6. Cat No: DIA-138. | |
| Cholesterol oxidase from Nocardia sp., Recombinant | Cholesterol oxidase (CHOD) is a monomeric flavoprotein containing FAD that catalyzes the first step in cholesterol catabolism. This bifunctional enzyme oxidizes cholesterol to cholest-5-en-3-one in an FAD-requiring step, which is then isomerized to cholest-4-en-3-one with the release of H2O2. Group: Enzymes. Synonyms: EC 1.1.3.6, cholesterol-O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase; 9028-76-6. Enzyme Commission Number: EC 1.1.3.6. CAS No. 9028-76-6. CHOD. Activity: > 20 Units / mg. Storage: Below -20°C. Form: Lyophilized powder. Source: E. coli. Species: Nocardia sp. EC 1.1.3.6, cholesterol-O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase; 9028-76-6. Cat No: NATE-1033. | |
| Cholesterol Oxidase from Streptomyces sp. | Cholesterol oxidase (CHOD) is a monomeric flavoprotein containing FAD that catalyzes the first step in cholesterol catabolism. This bifunctional enzyme oxidizes cholesterol to cholest-5-en-3-one in an FAD-requiring step, which is then isomerized to cholest-4-en-3-one with the release of H2O2. Group: Enzymes. Synonyms: EC 1.1.3.6, cholesterol-O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase; 9028-76-6. Enzyme Commission Number: EC 1.1.3.6. CAS No. 9028-76-6. Activity: 15U/mg-solid or more. Storage: -20°C. Form: Freeze dried powder. Source: Streptomyces sp. EC 1.1.3.6, cholesterol-O2 oxidoreductase; 3β-hydroxy steroid oxidoreductase; 3β-hydroxysteroid:oxygen oxidoreductase; 9028-76-6. Cat No: NATE-0128. | |
| Cholesterol oxidase, Microorganism | Cholesterol oxidase, Microorganism (ChOx) is a bacterial flavin oxidase containing FAD, commonly used in biochemical research. Cholesterol oxidase catalyzes the oxidation of the C(3)-OH group of cholesterol (and other sterols) to cholest-5-en-3-one and isomerizes it to cholest-4-en-3-one [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ChOx. CAS No. 9028-76-6. Pack Sizes: 100 U; 500 U; 1 KU. Product ID: HY-P2848. | |
| Cholesterol Oxidase, PEG Modified | PEG (Polyethylene glycol) modified cholesterol oxidase (Cholesterol oxidase PEG) is one of our premier cholesterol oxidase conjugates. Cholesterol oxidase is an enzyme that catalyzes the oxidation of cholesterol by oxygen into cholest-4-en-3-one and H2O2. This enzyme belongs to the family of oxidoreductases. Cholesterol oxidase has been used widely in the determination of serum cholesterol combined with other enzymes. PEG modified cholesterol oxidase provides better stability of this enzyme without major compromising its bioactivity. All our labeled cholesterol oxidase products were performed under mild reaction conditions to retain their maximum bioactivity. These conjugates were further purified by chromatography to ensure adequate applications both in-vitro and in-vivo. Conjugate ration: 20~50 peg5000r. solubility: soluble in aqueous buffer. Group: Enzymes. Synonyms: PEG Cholesterol Oxidase; Cholesterol Oxidase-polyethylene glycol; CHOD-polyethylene glycol; CHOD-PEG; PEG-CHOD; PEG-Cholesterol Oxidase. CHOD. Mole weight: ~61.8 kD. Activity: >10 units/mg solid. Storage: Store at -20°C. Form: Lyophilized powder. Source: Microorganism. PEG Cholesterol Oxidase; Cholesterol Oxidase-polyethylene glycol; CHOD-polyethylene glycol; CHOD-PEG; PEG-CHOD; PEG-Cholesterol Oxidase; Cholesterol Oxidase, PEG Modified. Cat No: NATE-1588. | |
| Cholesterol Palmitate | Cholest-5-en-3-ol (3b)-, 3-hexadecanoate. CAS No. 601-34-3. Product ID: 2-08403. Molecular formula: C43H76O2. Mole weight: 625.06. | |
| Cholesterol Palmitate, ≥97% | Solid. Group: Liquid crystal (lc) materials. CAS No. 601-34-3. Product ID: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] hexadecanoate. Molecular formula: 625.1g/mol. Mole weight: C43H76O2. CCCCCCCCCCCCCCCC (=O)OC1CCC2 (C3CCC4 (C (C3CC=C2C1)CCC4C (C)CCCC (C)C)C)C. InChI= 1S / C43H76O2 / c1-7-8-9-10-11-12-13-14-15-16-17-18-1 9-23-41 (44) 45-36-28-30-42 (5) 35 (32-36) 24-25-37-39-27-26-38 (34 (4) 22-20-21-33 (2) 3) 43 (39, 6) 31-29-40 (37) 42 / h24, 33-34, 36-40H, 7-23, 25-32H2, 1-6H3 / t34-, 36 + , 37 + , 38-, 39 + , 40 + , 42 + , 43- / m1 / s1. BBJQPKLGPMQWBU-JADYGXMDSA-N. | |
| Cholesterol palmitate methyl-ß-cyclodextrin complex | Cholesterol palmitate methyl-ß-cyclodextrin complex. Product ID: 4-00445. Purity: ~2 w/w% cholesterol. | |
| Cholesterol-PEG 600 | Cholesterol-PEG 600 is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 69068-97-9. Pack Sizes: 50 mg; 100 mg. Product ID: HY-W127558. | |
| Cholesterol Pelargonate | Cholesterol Pelargonate. Group: Liquid crystal (lc) building blocks. CAS No. 1182-66-7. Product ID: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] nonanoate. Molecular formula: 526.9g/mol. Mole weight: C36H62O2. CCCCCCCCC (=O)OC1CCC2 (C3CCC4 (C (C3CC=C2C1)CCC4C (C)CCCC (C)C)C)C. InChI=1S / C36H62O2 / c1-7-8-9-10-11-12-16-34 (37) 38-29-21-23-35 (5) 28 (25-29) 17-18-30-32-20-19-31 (27 (4) 15-13-14-26 (2) 3) 36 (32, 6) 24-22-33 (30) 35 / h17, 26-27, 29-33H, 7-16, 18-25H2, 1-6H3 / t27-, 29+, 30+, 31-, 32+, 33+, 35+, 36- / m1 / s1. WCLNGBQPTVENHV-MKQVXYPISA-N. | |
| Cholesterol Pelargonate, ≥93% | Cholesterol Pelargonate, ≥93%. Group: Liquid crystal (lc) materials. CAS No. 1182-66-7. Product ID: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] nonanoate. Molecular formula: 526.9g/mol. Mole weight: C36H62O2. CCCCCCCCC (=O)OC1CCC2 (C3CCC4 (C (C3CC=C2C1)CCC4C (C)CCCC (C)C)C)C. InChI=1S / C36H62O2 / c1-7-8-9-10-11-12-16-34 (37) 38-29-21-23-35 (5) 28 (25-29) 17-18-30-32-20-19-31 (27 (4) 15-13-14-26 (2) 3) 36 (32, 6) 24-22-33 (30) 35 / h17, 26-27, 29-33H, 7-16, 18-25H2, 1-6H3 / t27-, 29+, 30+, 31-, 32+, 33+, 35+, 36- / m1 / s1. WCLNGBQPTVENHV-MKQVXYPISA-N. | |
| Cholesterol phenylacetate | Cholesterol phenylacetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Phenylacetic Acid Cholesterol Ester; O-Phenylacetyl-cholesterin; CHOLESTEROL PHENYLACETATE; cholesteryl phenylacetate; Cholest-5-en-3beta-yl phenylacetate; Cholesterol Phenylacetate; Cholesteryl phenylacetate; O-phenylacetyl-cholesterol; EINECS 251-781-1. CAS No. 33998-26-4. Molecular formula: C35H52O2. Mole weight: 504.8. Purity: 94%+. IUPACName: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]2-phenylacetate. Canonical SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)CC5=CC=CC=C5)C)C. Density: 1.03g/cm³. ECNumber: 251-781-1. Product ID: ACM33998264. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholesterol, Plant-Derived | PharmaGrade, USP/NF, Ph Eur, Manufactured under appropriate GMP controls for pharma or biopharmaceutical production. Group: Fluorescence/luminescence spectroscopy. | |
| Cholesterol (powder) | 100g Pack Size. Group: Analytical Reagents, Aroma Chemicals, Biochemicals, Building Blocks, Flavours and Fragrance Materials. Formula: C27H46O. CAS No. 57-88-5. Prepack ID 90027949-100g. Molecular Weight 386.65. See USA prepack pricing. |  |
| Cholesterol propionate methyl-ß-cyclodextrin complex | Cholesterol propionate methyl-ß-cyclodextrin complex. Product ID: 4-00443. Purity: ~2 w/w% cholesterol. | |
| Cholesterol (Standard) | Cholesterol (Standard) is the analytical standard of Cholesterol. This product is intended for research and analytical applications. Cholesterol is the major sterol in mammals. It is making up 20-25% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins [1] [2]. Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist [3]. Uses: Scientific research. Group: Natural products. CAS No. 57-88-5. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-N0322R. | |
| Cholesterol Sulfate Potassium salt | selectively activates retinoid X receptors (RXRs). CAS No. 6614-96-6. Product ID: 8-01686. Molecular formula: C27H45KO4S. Mole weight: 504.81. Purity: 0.98. Properties: mp 223-225°C. | |
| Cholesterol synthetic | 1g Pack Size. Group: Analytical Reagents, Biochemicals, Building Blocks, Organics. Formula: C H O. CAS No. 57-88-5. Prepack ID 54776016-1g. Molecular Weight 386.65. See USA prepack pricing. | |
| Cholesterol valerate | Cholesterol valerate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Valeric Acid Cholesterol Ester. Product Category: Heterocyclic Organic CompoundCholesteryl Esters. Appearance: Powder to crystal. CAS No. 7726-3-6. Molecular formula: C32H54O2. Mole weight: 470.8. Purity: 99%+. Product ID: ACM7726036. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholesteryl 11-14 eicosadienoate | Cholesteryl 11-14 eicosadienoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (11Z,14Z)-11,14-Lcosadienoic acid 3β-cholesteryl ester. Product Category: Cholesteryl Esters. CAS No. 70110-48-4. Molecular formula: C47H80O2. Mole weight: 677.14. Purity: 95%+. IUPACName: [(3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] (11E,14E)-icosa-11,14-dienoate. Canonical SMILES: CCCCCC=CCC=CCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCCC(C)C)C)C. Product ID: ACM70110484. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholesteryl 11-eicosenoate | Cholesteryl 11-eicosenoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3β-Hydroxy-5-cholestene 3-(11-eicosenoate). Product Category: Heterocyclic Organic CompoundCholesteryl Esters. Appearance: Solid. CAS No. 70832-37-0. Molecular formula: C47H82O2. Mole weight: 679.2. Purity: 99%+. IUPACName: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] (E)-icos-11-enoate. Product ID: ACM70832370. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholesteryl-25,26,26,26,27,27,27,-d7 sulfate salt | ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Cholesteryl 2-naphthoate | Powder. Synonyms: 2-Naphthoic acid cholesteryl ester. Pack Sizes: 2g. Product ID: FR-2383. M.P. 166. Mole weight: 540.83. |  Frinton Laboratories |
| Cholesteryl 3?-N-(di-methyl-amino-ethyl)-carbamate hydrochloride | ?95%. Group: Fluorescence/luminescence spectroscopy. | |
| Cholesteryl 9-anthracenecarboxylate | Powder, 98%. Synonyms: 9-Anthracenecarboxylic acid cholesteryl ester. CAS No. 2641-40-9. Pack Sizes: 0.5g, 5g. Product ID: FR-2381. M.P. 194-196. Mole weight: 590.89. | Frinton Laboratories |
| Cholesteryl acetate | 97%. Group: Liquid crystals. | |
| Cholesteryl acetate | 25g Pack Size. Group: Biochemicals. Formula: C29H48O2. CAS No. 604-35-3. Prepack ID 11278658-25g. Molecular Weight 428.69. See USA prepack pricing. | |
| Cholesteryl acetate | Cholesteryl acetate - Product ID: NST-10-92. Category: Sterols. Alternative Names: Acebrochol, Cholesterol, Cholesterin. Purity: 98%. Test method: HPLC. CAS No. 604-35-3. Pack Sizes: 5g, 10g, 25g, 50g. Appearance: White to beige colored powder. Molecular formula: C29H48O2. Mole weight: 428.7. Storage: +2 +8 °C. |  |
| Cholesteryl acetate | Cholesteryl acetate (Cholesterol 3-acetate) is a cholesterol ester [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Cholesterol 3-acetate; Cholesterin acetate; Cholesterol 3β-acetate. CAS No. 604-35-3. Pack Sizes: 50 mg; 100 mg. Product ID: HY-107823. | |
| Cholesteryl Acetate | Cholesterol is a major component of all biological membranes; Cholesterol was found in all body tissues, especial in the brain, spinal cord, and in animal fats or oils. Group: Liquid crystal (lc) materials. Alternative Names: 3β-Acetoxy-5-cholestene. CAS No. 604-35-3. Pack Sizes: 25 kg/DRUMS. Product ID: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate. Molecular formula: 428.69. Mole weight: C29H48O2. XUGISPSHIFXEHZ-VEVYEIKRSA-N. 95%. | |
| Cholesteryl arachidonate | Cholesteryl arachidonate is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 604-34-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-113369. | |
| Cholesteryl arachidonate | ?95% (HPLC; detection at 205 nm), viscous liquid. Group: Fluorescence/luminescence spectroscopy. | |
| Cholesteryl Benhenate | Cholesteryl Benhenate. CAS No. 61540-09-6. Product ID: PE-0342. Category: Excipients. Product Keywords: Pharmaceutical Excipients; Excipients; Cholesteryl Benhenate; PE-0342; 61540-09-6; 61540-09-6. Sample Provided: No. Standard: ChP. Grade: Cosmeutical grade. | |
| Cholesteryl benzoate | Cholesteryl benzoate. Group: Liquid crystal (lc) materials. Alternative Names: 3-Hydroxycholest-5-ene3-benzoate. CAS No. 604-32-0. Product ID: [(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] benzoate. Molecular formula: 490.76. Mole weight: C34H50O2. C[C@H] (CCCC (C)C)[C@H]1CC[C@@H]2[C@@]1 (CC[C@H]3[C@H]2CC=C4[C@@]3 (CC[C@@H] (C4)OC (=O)C5=CC=CC=C5)C)C. InChI=1S/C34H50O2/c1-23 (2)10-9-11-24 (3)29-16-17-30-28-15-14-26-22-27 (36-32 (35)25-12-7-6-8-13-25)18-20-33 (26, 4)31 (28)19-21-34 (29, 30)5/h6-8, 12-14, 23-24, 27-31H, 9-11, 15-22H2, 1-5H3/t24-, 27+, 28+, 29-, 30+, 31+, 33+, 34-/m1/s1. UVZUFUGNHDDLRQ-LLHZKFLPSA-N. 98%+. | |
| Cholesteryl Benzoate | Off-white powder, 95%. CAS No. 604-32-0. Pack Sizes: 25g, 100g. Product ID: FR-0276. M.P. 148 (Ch), 176 (I). Mole weight: 490.77. | Frinton Laboratories |
| Cholesteryl bromide | Cholesteryl bromide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (3beta)-cholest-5-en;3-bromo-,(3.beta.)-Cholest-5-ene;CHOLESTERYL BROMIDE;5-CHOLESTENE-3-BETA-BROMO;3BETA-BROMO-5-CHOLESTENE;3beta-bromocholest-5-ene;3β-Bromo-5-cholestene;Cholesteryl Bromide from Beef Fat. Product Category: Steroidal Compounds. CAS No. 516-91-6. Molecular formula: C27H45Br. Mole weight: 449.55. Purity: 0.98. IUPACName: (3S,8S,9S,10R,13R,14S,17R)-3-bromo-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene. Canonical SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)Br)C)C. Density: 1.1g/cm³. ECNumber: 208-227-9. Product ID: ACM516916. Alfa Chemistry ISO 9001:2015 Certified. | |
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