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7208-47-1

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7208-47-1 Usage

General Description

Sorbitol Hexaacetate is an organic chemical compound derived from sorbitol, a type of sugar alcohol. It is produced through the process of acetylation, which introduces acetyl groups into the sorbitol molecule resulting in six acetyl groups, hence the term "hexaacetate". This substance is often used in synthetic organic chemistry as it acts as a protective agent and intermediate for various products. It is also commonly used in applications that require moderate reactivity and stability. However, like many chemicals, it needs to be handled with care as it can pose some health risks in certain conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 7208-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7208-47:
(6*7)+(5*2)+(4*0)+(3*8)+(2*4)+(1*7)=91
91 % 10 = 1
So 7208-47-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H26O12/c1-9(19)25-7-15(27-11(3)21)17(29-13(5)23)18(30-14(6)24)16(28-12(4)22)8-26-10(2)20/h15-18H,7-8H2,1-6H3/t15-,16+,17-,18-/m1/s1

7208-47-1 Well-known Company Product Price

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  • Aldrich

  • (146080)  D-Sorbitolhexaacetate  97%

  • 7208-47-1

  • 146080-25G

  • 776.88CNY

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7208-47-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name SORBITOL HEXAACETATE

1.2 Other means of identification

Product number -
Other names D-sorbitol hexaacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7208-47-1 SDS

7208-47-1Relevant articles and documents

Structural features and antioxidant activity of a new galactoglucan from edible mushroom Pleurotus djamor

Maity, Gajendra Nath,Maity, Prasenjit,Khatua, Somanjana,Acharya, Krishnendu,Dalai, Sudipta,Mondal, Soumitra

, p. 743 - 749 (2020/12/07)

A new water soluble galactoglucan with apparent molecular weight ~1.61 × 105 Da, was isolated from the edible mushroom Pleurotus djamor by hot water extraction followed by purification through dialysis tubing cellulose membrane and sepharose 6B column chromatography. The sugar analysis showed the presence of glucose and galactose in a molar ratio of nearly 3:1 respectively. The structure of the repeating unit in the polysaccharide was determined through chemical and NMR experiments as:[Formula presented] In vitro antioxidant studies showed that the PDPS exhibited hydroxyl radical scavenging activity (EC50 = 1.681 ± 0.034 mg/mL), DPPH radical scavenging activity (EC50 = 3.83 ± 0.427 mg/mL), reducing power (EC50 = 4.258 ± 0.095 mg/mL), and ABTS radical quenching activity (EC50 = 0.816 ± 0.077 mg/mL). So, PDPS should be explored as a natural antioxidant.

Isolation, purification and structural characterization of a water-soluble polysaccharide HM41 from Halenia elliptica D. Don

Liu, Chun-Lan,Li, Yang,Xu, Gui-Yun,Li, Ya-Shuang

, p. 979 - 983 (2016/06/13)

A water-soluble polysaccharide, HM41, was obtained from Halenia elliptica D. Don by acidic ethanol fractionation and gel filtration. Its homogeneity was confirmed by chromatography using multiple systems. HM41 was composed of rhamnose (Rha), arabinose (Ara), xylose (Xyl), mannose (Man), galactose (Gal), glucose (Glc) with a molar ratio of 1.0:5.5:1.8:3.0:9.4:21. The average molecular weight of HM41 was approximately 1.17 × 104. Periodate oxidation, Smith degradation, methylation and GC, IR, NMR, XRD, GC-MS analysis were used for the structural analysis of HM41. Its main chain was composed mainly of β-(1 → 4)Gal, β-(1 → 4)Glc and β-(1 → 6)Glc. β-(1 → 4)Gal were substituted at 6-O and on average there were 14 branches among 23 main chain residues; (1 → 4)Glc had no branch; (1 → 6)Glc were substituted at 3-O and on average there were 9 branches among 14 main chain residues. The side chain was composed of (1 → 3,6)-Rha, (1 → 4)/(1 → 5)-Ara, (1 → 4)/(1 → 5)-Xyl, (1 → 4,6)-Man and (1 → 2)-Glc. The terminal residue was composed of Ara, Xyl, Man, Gal, and Glc. Then, we demonstrated that HM and HM41 had strong scavenging activities in vitro hydroxyl. Overall, HM and HM41 may have potential applications in the antioxidants for medical and food industry.

Cu(ClO4)2·6H2O catalyzed solvent free per-O-acetylation and sequential one-pot conversions of sugars to thioglycosides

Chatterjee, Debnath,Paul, Abhijit,Rajkamal,Yadav, Somnath

, p. 29669 - 29674 (2015/05/20)

The solvent free per-O-acetylation of various reducing and non-reducing sugars has been carried out using stoichiometric amounts of acetic anhydride and copper(ii) perchlorate hexahydrate as the catalyst. The reactions with various reducing monosaccharides have also been followed by a one-pot sequential conversion to the corresponding thioglycosides in high yields. This journal is

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