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14307-17-6

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14307-17-6 Usage

Aminosugar

sugar molecule containing an amino group
Potential applications in food industry for chelating metal ions and as a prebiotic
Potential applications in pharmaceutical industry for anti-inflammatory and immunomodulatory properties
Studied for potential role in protecting skin from UV-induced damage
Potential ingredient in cosmetic and skincare formulations

Check Digit Verification of cas no

The CAS Registry Mumber 14307-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,0 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14307-17:
(7*1)+(6*4)+(5*3)+(4*0)+(3*7)+(2*1)+(1*7)=76
76 % 10 = 6
So 14307-17-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO6/c7-2(1-8)3(9)4(10)5(11)6(12)13/h1-5,9-11H,7H2,(H,12,13)/t2-,3+,4+,5-/m0/s1

14307-17-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-2-deoxy-D-galacturonic acid

1.2 Other means of identification

Product number -
Other names (2S,3R,4R,5R)-5-Amino-2,3,4-trihydroxy-6-oxo-hexanoic acid

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:14307-17-6 SDS

14307-17-6Upstream product

14307-17-6Downstream Products

14307-17-6Relevant articles and documents

Occurrence of 2 amino 2 deoxy hexuronic acids as constituents of Vibrio parahaemolyticus K15 antigen

Torii,Sakakibara,Kuroda

, p. 401 - 405 (2007/10/12)

Acidic capsular polysaccharide of V. parahaemolyticus A55 (05:K15) was esterified with ethylene oxide and then reduced with sodium borohydride. Hydrolysis of the reduced material gave two hexosamines identical with mannosamine (2 amino 2 deoxy mannose) an

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