CAS Number83465-22-9
Synonyms(2S)-2,4-Diamino-3-methyl-1-butanol; Valiolamine hydrate; Valinolamine; valiolamine; MFCD07773061; (1S,2S,3R,4S,5S)-5-AMINO-1-HYDROXYMETHYL-CYCLOHEXANE-1,2,3,4-TETRAOL
Molecular FormulaC7H15O5N1
Molecular Weight193.2
Purity98%
Density1.0±0.1 g/cm3
Boiling Point249.1±25.0 °C at 760 mmHg
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 83465-22-9 |
| Catalog No. | 2A-9008900 |
| Chinese Name | 井冈霉醇胺 |
| Synonyms | (2S)-2,4-Diamino-3-methyl-1-butanol; Valiolamine hydrate; Valinolamine; valiolamine; MFCD07773061; (1S,2S,3R,4S,5S)-5-AMINO-1-HYDROXYMETHYL-CYCLOHEXANE-1,2,3,4-TETRAOL |
| Molecular Formula | C7H15O5N1 |
| Molecular Weight | 193.2 |
| Purity | 98 |
| Density | 1.0±0.1 g/cm3 |
| Boiling Point | 249.1±25.0 °C at 760 mmHg |
| Storage Condition | 2-8°C, protected from light, dry and sealed |
| Application | Valiolamine is an aminocyclic alcohol isolated from the fermentation broth of Streptomyces hygroscopicus. Valiolamine has potent alpha-glucosidase inhibitory activity against porcine intestinal sucras |
| HTC | 2922199090 |
| MDL Number | MFCD07773061 |
| SMILES | NC1CC(O)(CO)C(O)C(O)C1O |
| InChI | InChI=1S/C7H15NO5/c8-3-1-7(13,2-9)6(12)5(11)4(3)10/h3-6,9-13H,1-2,8H2/t3-,4-,5+,6-,7-/m0/s1 |
| InChI Key | VDLOJRUTNRJDJO-ZYNSJIGGSA-N |
| MSDS | msds/8900_1_83465_22_9.pdf |
| Use of | Valiolamine, an aminocyclitol has been isolated from the fermentation broth of Streptomyces hygroscopicus subsp. Valiolamine has potent alpha-glucosidase inhibitory activity against porcine intestinal sucrase, maltase and isomaltase[1]. Properties Name (1S,2S,3R,4S,5S)-5-amino-1-(hydroxymethyl)cyclohexane-1,2,3,4-tetrol Synonym More Synonyms Valiolamine Biological Activity Description Valiolamine, an aminocyclitol has been isolated from the fermentation broth of Streptomyces hygroscopicus subsp. Valiolamine has potent alpha-glucosidase inhibitory activity against porcine intestinal sucrase, maltase and isomaltase[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Y Kameda, et al. Valiolamine, a New Alpha-Glucosidase Inhibiting Aminocyclitol Produced by Streptomyces Hygroscopicus. J Antibiot (Tokyo). 1984 Nov;37(11):1301-7. Chemical & Physical Properties Molecular Formula C7H15NO5 Exact Mass 118.110611 PSA 72.27000 LogP -1.60 Index of Refraction 1.490 InChIKey VDLOJRUTNRJDJO-ZYNSJIGGSA-N Toxicological Information CHEMICAL IDENTIFICATION RTECS NUMBER : CHEMICAL NAME : D-epi-Inositol, 4-amino-3,4-dideoxy-2-C-(hydroxymethyl)-, hydrate CAS REGISTRY NUMBER : 83465-22-9 LAST UPDATED : DATA ITEMS CITED : MOLECULAR FORMULA : C7-H15-N-O5.H2-O MOLECULAR WEIGHT : HEALTH HAZARD DATA ACUTE TOXICITY DATA TYPE OF TEST : LD - Lethal dose ROUTE OF EXPOSURE : Unreported SPECIES OBSERVED : Rodent - rat DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : EPXXDW European Patent Application. (U.S. Patent and Trademark Office, Foreign Patents, Washington, DC 20231) Volume(issue)/page/year: #63456 Safety Information HS Code 2922199090 Synthetic Route tetra-O-benzylv... 140926-94-9 Valiolamine 83465-22-9 (4aS,6S,6aS,8R,... 1060713-64-5 Valiolamine 83465-22-9 Literature: Shing, Tony K. M.; Cheng, Hau M. Organic Letters, 2008 , vol. 10, # 18 p. 4137 - 4139 (1S,2S,3R,4S,5S... 183505-14-8 Valiolamine 83465-22-9 Literature: Shing, Tony K. M.; Wan, Leong H. Journal of Organic Chemistry, 1996 , vol. 61, # 24 p. 8468 - 8479 |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 30.0% |
| Transport Info | Product name: Summary 2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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