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| Product | Description | |
|---|---|---|
| CHO | CHO. Pack Sizes: 1 g. Product ID: PE-0358. Category: Lipid Excipients. Product Keywords: Pharmaceutical Excipients; Lipid Excipients; CHO; PE-0358. Purity: ≥99%. Application: Liposome and Micelle Formulations in Market. Product Description: Cholesterol. |  |
| CHO Cell Transfection Reagent | Transfection Reagent for CHO Cells. Optimized transfection protocol provided for transfection of siRNA, DNA, mRNA, and microRNA. Transfection Reagents. Transfection Enhancer. Complex Condenser. Uses: Transfection of DNA, RNA, protein and small molecules. Product ID: 2066. |  Nevada, Texas, USA |
| Chocolate Brown HT | Chocolate Brown HT. Group: Biochemicals. Alternative Names: Food Brown 3; CI 2285. Grades: Highly Purified. CAS No. 4553-89-3. Pack Sizes: 50g, 100g, 250g, 500g, 1Kg. Molecular Formula: C27H18N4O9S2·2Na. US Biological Life Sciences. |  Worldwide |
| Chocovan Tec Ab 7244c | Chocovan Tec Ab 7244c. CAS No. MIXTURE. VIGON Item # 507971. Categories: Speciality Ingrdients Suppliers. |  America & Internationally |
| Chokeberry Extract | Chokeberry Extract. Applications: Used for health care products, dietary supplements, herb medecine beverage and cosmetic industry. Group: Others. Synonyms: Chokeberry Extract; Aronia Melanocarpa L. Purity: 5%-25% Anthocyanidins by UV, 4-50:1 by TLC. Appearance: Violet fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Fruit. Species: Aronia Melanocarpa L. Chokeberry Extract; Aronia Melanocarpa L.; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-186. |  |
| Chola-3,5-dienic Acid Methyl Ester | Chola-3,5-dienic Acid Methyl Ester is an transformation product of Hyodeoxycholic Acid (H998100), an secondary bile acid that is the metabolic byproduct of intestinal bacteria. Group: Biochemicals. Alternative Names: Chola-3,5-dien-24-oic Acid Methyl Ester. Grades: Highly Purified. CAS No. 1172-10-7. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Cholan-24-oic acid, 3,7,12,23-tetrahydroxy-, (3α, 5β, 7α, 12α, 23S)- | Cas No. 181139-68-4. Molecular formula: C24H40O6. Mole weight: 424.57. |  |
| Cholane Related Compoumd 1 (5-alpha-Homopregnanic Acid) | impurity of cholane. Synonyms: Pregnane-20-carboxylic acid, (5α,?20S)?-. Grades: > 95%. CAS No. 34311-19-8. Molecular formula: C22H36O2. Mole weight: 332.53. | |
| Cholanic acid | Cholanic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CHOLANIC ACID;Einecs 246-816-2. Product Category: Heterocyclic Organic Compound. CAS No. 25312-65-6. Molecular formula: C24H40O2. Mole weight: 360.58. Product ID: ACM25312656. Alfa Chemistry ISO 9001:2015 Certified. |  |
| cholate-CoA ligase | Requires Mg2+ for activity. The mammalian enzyme is membrane-bound and catalyses the first step in the conjugation of bile acids with amino acids, converting bile acids into their acyl-CoA thioesters. Chenodeoxycholate, deoxycholate, lithocholate and trihydroxycoprostanoate can also act as substrates. The bacterial enzyme is soluble and participates in an anaerobic bile acid 7 α-dehydroxylation pathway. Group: Enzymes. Synonyms: BAL; bile acid CoA ligase; bile acid co. Enzyme Commission Number: EC 6.2.1.7. CAS No. 9027-90-1. 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-5709; cholate-CoA ligase; EC 6.2.1.7; 9027-90-1; BAL; bile acid CoA ligase; bile acid coenzyme A ligase; choloyl-CoA synthetase; choloyl coenzyme A synthetase; cholic thiokinase; cholate thiokinase; cholic acid:CoA ligase; 3α,7α,12α-trihydroxy-5β-cholestanoyl coenzyme A synthetase; 3α,7α,12α-trihydroxy-5β-cholestanoate-CoA ligase; 3α,7α,12α-trihydroxy-5β-cholestanoate-CoA synthetase; THCA-CoA ligase; 3α,7α,12α-trihydroxy-5β-cholestanate-CoA ligase; 3α,7α,12α-trihydroxy-5β-cholestanate:CoA ligase (AMP-forming); cholyl-CoA synthetase; trihydroxycoprostanoyl-CoA synthetase. Cat No: EXWM-5709. | |
| Cholecalciferol | Cholecalciferol. Group: Biochemicals. Alternative Names: Vitamin D3. Grades: Highly Purified. CAS No. 67-97-0. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C27H44O. US Biological Life Sciences. | Worldwide |
| Cholecalciferol | Cholecalciferol is a naturally occuring form of vitamin D. Reported that upon metabolic activation, Cholecalciferol induces cell differentiation and prevents proliferation of cancer cells. Cholecalciferol is an activator of VDR. Applications: An unhydroxylated form of vitamin d3. Group: Coenzymes. Synonyms: Vitamin D3; Activated 7-dehydrocholesterol; Calciol. CAS No. 67-97-0. Purity: ≥98%. Mole weight: 384.64. Appearance: Crystalline powder. Form: Solid. Vitamin D3; Activated 7-dehydrocholesterol; Calciol; Cholecalciferol; 67-97-0. Cat No: COEC-011. | |
| Cholecalciferol, 100IU/mg | Potency: Group: Biochemicals. Alternative Names: Vitamin D3. Grades: Highly Purified. CAS No. 67-97-0. Pack Sizes: 500g, 1kg, 2kg, 5kg, 10kg. US Biological Life Sciences. | Worldwide |
| Cholecalciferol, 97.0-103.0% (HPLC) USP | Cholecalciferol, 97.0-103.0% (HPLC) USP. Group: Biochemicals. Grades: USP. CAS No. 67-97-0. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| Cholecalciferol glucuronide | A metabolite of Vitamin D3. Synonyms: (3b,5Z,7E)-9,10-Secocholesta-5,7,10(19)-trien-3-yl. Grades: > 95%. CAS No. 57918-08-8. Molecular formula: C33H52O7. Mole weight: 560.76. | |
| Cholecalciferol Impurity A | Cas No. 22350-41-0. | |
| Cholecalciferol Impurity C | Cas No. 5226-1-7. | |
| Cholecalciferol Impurity D | Cas No. 22350-43-2. | |
| Cholecalciferol Impurity E | Cas No. 17592-07-3. | |
| Cholecalciferol sulfate Sodium Salt | The main metabolite of Vitamin D3. It has potent biological activity. Vitamin D3-sulfate had <5% of the activity of vitamin D3 to mobilize Ca from bone and.apprx.1% of the ability of Vitamin D3 to stimulate Ca transport, elevate serum P, or support bone calcification. Synonyms: Vitamin D3 Sulfate Sodium Salt; (1S,3Z)-3-[(2E)-2-[(1R,3aS,7aR)-1-[(1R)-1,5-Dimethylhexyl]octahydro-7a-methyl-4H-inden-4-ylidene]ethylidene]-4-methylenecyclohexanol Sodium Salt; (3β,5Z,7E)-9,10-Secocholesta-5,7,10(19)-trien-3-ol Ηydrogen Sulfate Sodium Salt. Grades:> 95%. CAS No. 78392-27-5. Molecular formula: C27H44O4S`Na. Mole weight: 464.71 23. | |
| Cholecalciferol USP | Calciol, vitamin D3, activated 7-dehydrocholesterol. veterinary drug. Grades: USP. CAS No. 67-97-0. Product ID: 8-01414. Molecular formula: C27H44O. Mole weight: 384.64. |  |
| Cholecalciferol (Vitamin D3, Activated 7-dehydrocholesterol) | Vitamin D3 is cholecalciferol, one of the vitamin D family. Vitamin D3 has been used to prevent and treat breast cancer, prostate and possibly other cancers and Vitamin D3 is essential to maintain bone density. Vitamin D3 is necessary for the ultilization of Calcium and Phosphorus, and for the assimilation of Vitamin A. It also has a strong immune enhancing effect. In many ways vitamin D acts as a hormone and is potent in minute quantities. One microgram of cholecalciferol has 40 IU of vitamin D activity. Vitamin D is necessary for utilization of calcium and phosphorus. Activated 7-dehydrocholesterol, cholecalciferol, also called activated 7-dehydrocholesterol, cholecalciferol. The biologically active form of Vitamin D. It is transported by the blood and the liver converts it to 25-Hydroxycholecalciferol (25-Hydroxyvitamin D, Calcidiol) which is converted in the kidneys to 1, 25-Di hydroxycholecalciferol (1,25-Dihydroxyvitamin D, Calcitriol). Group: Biochemicals. Alternative Names: Vitamin D3; Activated 7-dehydrocholesterol. Grades: Cell Culture Grade. CAS No. 67-97-0. Pack Sizes: 1g, 5x1g. US Biological Life Sciences. | Worldwide |
| Cholecystokinin | Cholecystokinin is a peptide hormone. Cholecystokinin, as a hunger suppressant, inhibits food intake and stimulates the digestion of fat and protein. Cholecystokinin can be used for the research of gastrointestinal system [1] [2] [3]. Uses: Scientific research. Group: Peptides. Alternative Names: Cholecystokinin-33(human); CCK-33(human). CAS No. 9011-97-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P2932. |  |
| Cholecystokinin (26-33) (free acid) | Cholecystokinin (26-33) (CCK (26-33)) free acid is a cholecystokinin (CCK) fragment. Cholecystokinin (26-33) free acid can reduce food intake and gallbladder contraction [1]. Uses: Scientific research. Group: Peptides. Alternative Names: CCK (26-33) (free acid). CAS No. 103974-46-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P3651. | |
| Cholecystokinin-33 (human) | Cholecystokinin-33 (human) is a peptide hormone, holding great significance in biomedical research as it enables exploration into the intricacies of cholecystokinin receptors. Synonyms: CCK-39 (7-39) (human); H-Lys-Ala-Pro-Ser-Gly-Arg-Met-Ser-Ile-Val-Lys-Asn-Leu-Gln-Asn-Leu-Asp-Pro-Ser-His-Arg-Ile-Ser-Asp-Arg-Asp-Tyr(SO3H)-Met-Gly-Trp-Met-Asp-Phe-NH2; L-lysyl-L-alanyl-L-prolyl-L-seryl-glycyl-L-arginyl-L-methionyl-L-seryl-L-isoleucyl-L-valyl-L-lysyl-L-asparagyl-L-leucyl-L-glutaminyl-L-asparagyl-L-leucyl-L-alpha-aspartyl-L-prolyl-L-seryl-L-histidyl-L-arginyl-L-isoleucyl-L-seryl-L-alpha-aspartyl-L-arginyl-L-alpha-aspartyl-O4-sulfo-L-tyrosyl-L-methionyl-glycyl-L-tryptophyl-L-methionyl-L-alpha-aspartyl-L-phenylalaninamide. Grades: ≥90%. CAS No. 96827-04-2. Molecular formula: C167H263N51O52S4. Mole weight: 3945.44. | |
| Cholecystokinin (CCK) Fragment 26-33 Amide, Non-sulfated | ?95% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. |  |
| Cholecystokinin Fragment 30-33 Amide | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Cholecystokinin Precursor (24-32) (rat) | Cholecystokinin Precursor (24-32) (rat) is a cholecystokinin precursor that can be expressed in the heart, lungs, and kidneys as well as in the gastrointestinal tract and brain. Cholecystokinin is a brain-gut peptide that stimulates gallbladder contraction and pancreatic exocrine secretion and also acts as a neurotransmitter [1]. Uses: Scientific research. Group: Peptides. Alternative Names: Prepro CCK Fragment V-9-M. CAS No. 99291-20-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P2636. | |
| Cholecystokinin Precursor Fragment 107-115 Desulfated human | >97% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Cholera autoinducer 1 | Cholera autoinducer 1 is Vibrio cholerae autoinducer (S)-3-hydroxytridecan-4-one. Cholera autoinducer 1 influences chemotaxis in C. elegans [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CAI-1. CAS No. 1004296-82-5. Pack Sizes: 1 mg. Product ID: HY-145376. | |
| Cholera Autoinducer 1: (3S)-3-Hydroxy-4-tridecanone | Cholera Autoinducer 1: (3S)-3-Hydroxy-4-tridecanone is an extracellular quorum-sensing molecule which is responsible for the virulence production factor and biofilm development of Vibrio cholerae. Group: Biochemicals. Grades: Highly Purified. CAS No. 1004296-82-5. Pack Sizes: 5mg, 10mg. Molecular Formula: C13H26O2, Molecular Weight: 214.34. US Biological Life Sciences. | Worldwide |
| Cholera Toxin A Subunit from Vibrio cholerae | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Cholera Toxin B subunit | recombinant, expressed in HEK 293 cells, subunit A free. Group: Fluorescence/luminescence spectroscopy. | |
| Cholera toxin B subunit, from vibrio cholerae | Cholera toxin B subunit, from vibrio cholerae (CTB, from vibrio cholerae) is non-toxic to cells and possesses no intrinsic adenylate cyclase activity. Cholera toxin B subunit, from vibrio cholerae attaches to cells by binding to ganglioside GM1.8 CTB has been shown to be a good label for microglial cells (due to the enrichment of ganglioside GM1 on their cell surface), but not for oligodendrocytes or astrocytes. Cholera toxin B subunit, from vibrio cholerae has been reported to be an excellent tracer for the study of axonal transport using immunohistochemical methods. Cholera toxin B subunit, from vibrio cholerae has been widely used as a marker of membrane lipid rafts [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: CTB, from vibrio cholerae. CAS No. 131096-89-4. Pack Sizes: 500 μg; 1 mg. Product ID: HY-P3394. | |
| Cholera Toxin from Vibrio cholerae | ~95% (SDS-PAGE), lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Cholessteryl Oleyl Carbonate | Cholesteric, 97%. CAS No. 17110-51-9. Pack Sizes: 25g. Product ID: FR-0423. M.P. 18 (Ch), 32 (I). Mole weight: 681.14. |  Frinton Laboratories |
| cholest-4-en-3-one 26-monooxygenase [(25R)-3-oxocholest-4-en-26-oate forming] | This enzyme, found in several bacterial pathogens, is involved in degradation of the host cholesterol. It catalyses the hydroxylation of the C-26 carbon, followed by oxidation of the alcohol to the carboxylic acid via the aldehyde intermediate, initiating the degradation of the alkyl side-chain of cholesterol. The products are exclusively in the (25R) conformation. The enzyme also accepts cholesterol as a substrate. cf. EC 1.14.13.141, cholest-4-en-3-one 26-monooxygenase. The enzyme can receive electrons from ferredoxin reductase in vitro, its natural electron donor is not known yet. Group: Enzymes. Synonyms: CYP142. Enzyme Commission Number: EC 1.14.13.221. 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-0824; cholest-4-en-3-one 26-monooxygenase [(25R)-3-oxocholest-4-en-26-oate forming]; EC 1.14.13.221; CYP142. Cat No: EXWM-0824. | |
| cholest-4-en-3-one 26-monooxygenase [(25S)-3-oxocholest-4-en-26-oate forming] | This enzyme, found in several bacterial pathogens, is involved in degradation of the host's cholesterol. It catalyses the hydroxylation of the C-26 carbon, followed by oxidation of the alcohol to the carboxylic acid via the aldehyde intermediate, initiating the degradation of the alkyl side-chain of cholesterol. The products are exclusively in the (25S) configuration. It is a two-component system consisting of a P-450 (heme thiolate) oxygenase (Cyp125) and a ferredoxin reductase (most likely KshB, which is also a part of EC 1.14.13.142, 3-ketosteroid 9α-monooxygenase). The enzyme also accepts cholesterol as a substrate. cf. EC 1.14.13.221, cholest-4-en-3-one 27-monooxygenase. Group: Enzymes. Synonyms: CYP125; CYP125A1; cholest-4-en-3-one 27-monooxygenase (misleading); cholest-4-en-3-one,NADH:oxygen oxidoreductase (26-hydroxyl. Enzyme Commission Number: EC 1.14.13.141. 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-0741; cholest-4-en-3-one 26-monooxygenase [(25S)-3-oxocholest-4-en-26-oate forming]; EC 1.14.13.141; CYP125; CYP125A1; cholest-4-en-3-one 27-monooxygenase (misleading); cholest-4-en-3-one,NADH:oxygen oxidoreductase (26-hydroxylating); cholest-4-en-3-one 26-monooxygenase (ambiguous). Cat No: EXWM-0741. | |
| Cholest-5-en-3beta-yl p-butoxybenzoate | Cholest-5-en-3beta-yl p-butoxybenzoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: EINECS 255-394-9, CID6451742, Cholest-5-en-3beta-yl p-butoxybenzoate, BAS 00124352, 41484-52-0. Product Category: Heterocyclic Organic Compound. CAS No. 41484-52-0. Molecular formula: C38H58O3. Mole weight: 562.865320 [g/mol]. Purity: 0.96. IUPACName: [(3S,10R,13R,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] 4-butoxybenzoate. Canonical SMILES: CCCCOC1=CC=C(C=C1)C(=O)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCCC(C)C)C)C. ECNumber: 255-394-9. Product ID: ACM41484520. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholest-5-en-3beta-yl p-ethoxybenzoate | Cholest-5-en-3beta-yl p-ethoxybenzoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: EINECS 255-393-3, CID6451741, Cholest-5-en-3beta-yl p-ethoxybenzoate, BAS 00124357, 41484-50-8. Product Category: Heterocyclic Organic Compound. CAS No. 41484-50-8. Molecular formula: C36H54O3. Mole weight: 534.812160 [g/mol]. Purity: 0.96. IUPACName: [(3S,10R,13R,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] 4-ethoxybenzoate. Canonical SMILES: CCOC1=CC=C(C=C1)C(=O)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCCC(C)C)C)C. ECNumber: 255-393-3. Product ID: ACM41484508. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholest-5-en-3beta-yl propionate | Cholest-5-en-3beta-yl propionate. Group: Liquid crystal (lc) building blocks. Alternative Names: 3β-propanoyloxycholest-5-ene. CAS No. 633-31-8. 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] propanoate. Molecular formula: 442.72. Mole weight: C30H50O2. CCC (=O)O[C@H]1CC[C@@]2 ([C@H]3CC[C@]4 ([C@H] ([C@@H]3CC=C2C1)CC[C@@H]4[C@H] (C)CCCC (C)C)C)C. InChI=1S/C30H50O2/c1-7-28 (31)32-23-15-17-29 (5)22 (19-23)11-12-24-26-14-13-25 (21 (4)10-8-9-20 (2)3)30 (26, 6)18-16-27 (24)29/h11, 20-21, 23-27H, 7-10, 12-19H2, 1-6H3/t21-, 23+, 24+, 25-, 26+, 27+, 29+, 30-/m1/s1. CCORPVHYPHHRKB-NXUCFJMCSA-N. 98%+. |  |
| Cholest-5-en-3-b-yl octadecanoate | Cholest-5-en-3-b-yl octadecanoate. Group: Biochemicals. Alternative Names: Cholesteryl stearate. Grades: Highly Purified. CAS No. 35602-69-8. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C45H80O2. US Biological Life Sciences. | Worldwide |
| Cholest-5-en-3-ol, 3- (6- ( ( (2-cyanoethoxy) (diisopropylamino) phosphino) oxy) hexyl) carbemate | Cholest-5-en-3-ol is a powerful substance that functions to combat hypercholesterolemia and various lipid disorders. Using innovative technology, it works to inhibit cholesterol synthesis in the liver, leading to the reduction of overall blood cholesterol levels. Due to its notable and demonstrated effectiveness, it is highly regarded and widely employed within the biopharmaceutical industry in the treatment of cardiovascular diseases. CAS No. 143723-64-2. | |
| Cholest-5-en-3-ol (3b)-, 3-(carbonochloridate) | Cholest-5-en-3-ol (3b)-, 3-(carbonochloridate). Group: Biochemicals. Grades: Highly Purified. CAS No. 7144-8-3. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C28H45ClO2. US Biological Life Sciences. | Worldwide |
| Cholest-5-en-3-ol, 3-CEphosphoramidite | Cholest-5-en-3-ol, 3-CEphosphoramidite, a versatile phosphoramidite reagent, is vital for modifying RNA and DNA analogs. Its immense value lies in its ability to assist in the treatment of varied afflictions including cancer, HIV, and genetic defects, making it a pivotal cog in the biomedical industry. Respected chemical suppliers globally procure and make it available. CAS No. 143723-63-1. | |
| cholest-5-ene-3β,7α-diol 3β-dehydrogenase | Highly specific for 3β-hydroxy-C27-steroids with Δ5-double bond. Group: Enzymes. Synonyms: 3β-hydroxy-Δ5-C27-steroid oxidoreductase. Enzyme Commission Number: EC 1.1.1.181. CAS No. 56626-16-5. 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-0084; cholest-5-ene-3β,7α-diol 3β-dehydrogenase; EC 1.1.1.181; 56626-16-5; 3β-hydroxy-Δ5-C27-steroid oxidoreductase. Cat No: EXWM-0084. | |
| Cholesta-3,5-diene | ?93% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Cholesta-4,6-dien-3-one | A metabolite of Cholesterol. Group: Biochemicals. Alternative Names: 4,6-Cholestadien-3-one; NSC 119073. Grades: Highly Purified. CAS No. 566-93-8. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Cholestan-3β,5α-diol | Cholestan-3β,5α-diol. Uses: Designed for use in research and industrial production. Product Category: Steroidal Compounds. CAS No. 3347-60-2. Molecular formula: C27H48O2. Mole weight: 404.67. Purity: 0.95. Product ID: ACM3347602. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholestan-5α,6β-diol | Cholestan-5α,6β-diol. Uses: Designed for use in research and industrial production. Product Category: Steroidal Compounds. CAS No. 566-31-4. Molecular formula: C27H48O2. Mole weight: 404.67. Purity: 0.95. Product ID: ACM566314. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholestan-5α-ol-3,6-dione | Cholestan-5α-ol-3,6-dione. Uses: Designed for use in research and industrial production. Product Category: Steroidal Compounds. CAS No. 20281-70-3. Molecular formula: C27H44O3. Mole weight: 416.64. Purity: 0.95. Product ID: ACM20281703. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholestan-5β,6β-epoxy-3β-ol | Cholestan-5β,6β-epoxy-3β-ol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5beta,6beta-Epoxycholestanol; CHOLESTEROL-5BETA,6BETA-EPOXIDE; 5,6beta-epoxy-5beta-cholestan-3beta-ol; 5BETA,6BETA-EPOXYCHOLESTAN-3BETA-OL; cholestanol,5ß,6ß-epo; cholesterol-5B,6B-epoxide; cholesterolbeta-epoxide. Product Category: Steroidal Compounds. CAS No. 4025-59-6. Molecular formula: C27H46O2. Mole weight: 402.65. Purity: 0.95. IUPACName: 5,6β-epoxy-5β-cholestan-3β-ol. Density: 1.04g/cm³. Product ID: ACM4025596. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cholestane-3b,5a,6b-triol | Cholestane-3b,5a,6b-triol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3beta,5alpha,6beta-Trihydroxycholestane; 3beta,5alpha,6beta-Cholestanetriol; Cholestane-3beta,5alpha,6beta-triol; Cholesta-3beta,5alpha,6beta-triol; cholestanetriol; 5alpha,6beta-Dihydroxycholestanol; 5alpha-cholestane-3beta,5,6beta-triol; (3S,5R,6R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol. Product Category: Steroidal Compounds. CAS No. 1253-84-5. Molecular formula: C27H48O3. Mole weight: 420.68. Purity: 0.95. IUPACName: (3S,5R,6R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol. Canonical SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C. Density: 1.065g/cm³. Product ID: ACM1253845. Alfa Chemistry ISO 9001:2015 Certified. | |
| cholestanetriol 26-monooxygenase | This mitochondrial cytochrome P-450 enzyme requires adrenodoxin. It catalyses the first three sterol side chain oxidations in bile acid biosynthesis via the neutral (classic) pathway. Can also act on cholesterol, cholest-5-ene-3β,7α-diol, 7α-hydroxycholest-4-en-3-one, and 5β-cholestane-3α,7α-diol. The enzyme can also hydroxylate cholesterol at positions 24 and 25. 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: 5β-cholestane-3α,7α,12α-triol 26-hydroxylase; 5β-cholestane-3α,7α,12α-triol hydroxylase; cholestanetriol 26-hydroxylase; sterol 27-hydroxylase; sterol 26-hydroxylase; cholesterol 27-hydroxyla. Enzyme Commission Number: EC 1.14.15.15. CAS No. 52227-77-7. 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-0940; cholestanetriol 26-monooxygenase; EC 1.14.15.15; 52227-77-7; 5β-cholestane-3α,7α,12α-triol 26-hydroxylase; 5β-cholestane-3α,7α,12α-triol hydroxylase; cholestanetriol 26-hydroxylase; sterol 27-hydroxylase; sterol 26-hydroxylase; cholesterol 27-hydroxylase; CYP27A; CYP27A1; cytochrome P450 27A1'. Cat No: EXWM-0940. | |
| cholestanol-d5 | cholestanol-d5. Group: Others. Purity: >99%. Mole weight: 393.7. Stability: 6 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; sterols; sterols products; singnal transduction; cell pathways; cholestanol-d5; 2,2,3,4,4-pentadeuterio-5a-cholestan-3ss-ol. Cat No: STEZ-073. | |
| cholestenoic acid-d5 | cholestenoic acid-d5. Group: Others. Purity: >99%. Mole weight: 421.667. Stability: 6 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; sterols; sterols products; singnal transduction; cell pathways; cholestenoic acid-d5; 3ss-hydroxy-5-cholestenoic acid-d5. Cat No: STEZ-036. | |
| cholestenol Δ-isomerase | This enzyme belongs to the family of isomerases, specifically those intramolecular oxidoreductases transposing C=C bonds. This enzyme participates in biosynthesis of steroids. Group: Enzymes. Enzyme Commission Number: EC 5.3.3.5. CAS No. 52410-46-5. 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-5502; cholestenol Δ-isomerase; EC 5.3.3.5; 52410-46-5. Cat No: EXWM-5502. | |
| Cholesterol | 100g Pack Size. Group: Biochemicals. Formula: C27H46O. CAS No. 57-88-5. Prepack ID 13575167-100g. Molecular Weight 386.65. See USA prepack pricing. |  |
| Cholesterol | 500g Pack Size. Group: Biochemicals. Formula: C27H46O. CAS No. 57-88-5. Prepack ID 13575167-500g. Molecular Weight 386.65. See USA prepack pricing. | |
| Cholesterol | Cholesterol. CAS No. 57-88-5. Product ID: PE-0315. Molecular formula: C27H46O. Mole weight: 386.66. Category: Micro-drug Delivery Systems. Product Keywords: Pharmaceutical Excipients; Micro-drug Delivery Systems; Cholesterol; PE-0315; C27H46O; 57-88-5; 57-88-5. Appearance: White powder. Purity: 0.99. EC Number: 200-353-2. Solubility: H2O: 0.002 mg/mL. Storage: -20°C. Boiling Point: 360 °C. Melting Point: 148-150 °C. Density: 1.06 g/cm3. | |
| Cholesterol | Cholesterol is a natural waxy substance that is found in human skin and is also commonly used in cosmetics and skincare products. In cosmetics, cholesterol is used as a moisturizer and emollient to help soften and smooth the skin, as well as to improve the appearance of fine lines and wrinkles. It is also believed to help strengthen the skin's barrier function and protect against environmental damage. The chemical formula of cholesterol is C27H46O, and it typically appears as a white or off-white powder or solid. It is also available in liquid form, often in combination with other ingredients. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3β-Hydroxycholest-5-ene. Product Category: Cholesteryl Esters. Appearance: White powder. CAS No. 57-88-5. Molecular formula: C27H46O. Mole weight: 386.66. Purity: 0.98. 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-ol. Canonical SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C. Density: 1.06 g/cm³. Product ID: ACM57885. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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: Natural products. CAS No. 57-88-5. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-N0322. | |
| Cholesterol | Cholesterol occurs as white or faintly yellow, almost odorless, pearly leaflets, needles, powder, or granules. On prolonged exposure to light and air, cholesterol acquires a yellow to tan color. Synonyms: Cholesterin; cholesterolum. CAS No. 57-88-5. Product ID: PE-0519. Molecular formula: C27H46O. Mole weight: 386.67. Category: Emollient; Emulsifying Agents. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0519; Cholesterol; Emollient; Emulsifying Agents; C27H46O; 57-88-5. UNII: 97C5T2UQ7J. Chemical Name: Cholest-5-en-3β-ol. Grade: Pharmceutical Excipients. Administration route: Injections; ophthalmic, topical, and vaginal. Dosage Form: Injections; ophthalmic, topical, and vaginal preparations. Stability and Storage Conditions: Cholesterol is stable and should be stored in a well-closed container, protected from light. Source and Preparation: The commercial material is normally obtained from the spinal cord of cattle by extraction with petroleum ethers, but it may also be obtained from wool fat. Purification is normally accomplished by repeated bromination. Cholesterol may also be produced by entirely synthetic means. Cholesterol produced from animal organs will always contain cholestanol and other saturated sterols. Applications: Cholesterol is used in cosmetics and topical pharmaceutical formulations at concentrations of 0.3-5.0% w/w as an emulsifying agent. It imparts water-absorbi | |
| Cholesterol | Cholesterol - Product ID: NST-10-135. Category: Sterols. Alternative Names: (-)-Cholesterol, Cholesteryl alcohol, Dythol, Lidinit, Marine Cholesterol, Provitamin D. Purity: 98%. Test method: HPLC. CAS No. 57-88-5. Pack Sizes: 50g, 100g, 250g, 500g. Appearance: White to beige coloured Powder. Molecular formula: C27H46O. Mole weight: 386.66. Storage: +2 +8 °C. |  |
| Cholesterol | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsnutritional composition compoundsbuilding blockseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Cholesterol (8CI),Cholesterol, Lidinit, Provitamin D, SyntheChol, NSC 8798, Cholesterin, (-)-Cholesterol, Cholesteryl alcohol, Dythol, Lidinite. | |
| Cholesterol-13C2 | Cholesterol- 13 C 2 is the 13 C 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. 78887-48-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N0322S5. | |
| Cholesterol-2,2,3,4,4,6-d6 | 97 atom % D, 98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Cholesterol-2,2,3,4,4,6-d6 | Cholesterol-2,2,3,4,4,6-d6. Group: Biochemicals. Grades: Highly Purified. CAS No. 92543-08-3. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C27D6H40O. US Biological Life Sciences. | Worldwide |
| Cholesterol-23,24,25,26,27-13C5 | ?99 atom % 13C, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Cholesterol-2,3,4-13C3 | 99 atom % 13C, 98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
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