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1200446-88-3

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1200446-88-3 Usage

Uses

The R-enatiomer of (3S)-β-Cryptoxanthin (C827500), a natural caratenoid pigment that is an antioxidant which helps prevent free radical damage to cells and DNA as well as being a potential chemopreventative agent against lung cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 1200446-88-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,0,4,4 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1200446-88:
(9*1)+(8*2)+(7*0)+(6*0)+(5*4)+(4*4)+(3*6)+(2*8)+(1*8)=103
103 % 10 = 3
So 1200446-88-3 is a valid CAS Registry Number.

1200446-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-β-Cryptoxanthin

1.2 Other means of identification

Product number -
Other names (1S)-3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohex-3-en-1-ol

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:1200446-88-3 SDS

1200446-88-3Downstream Products

1200446-88-3Relevant articles and documents

Synthesis of (3S)- and (3R)-3-hydroxy-β-ionone and their transformation into (3S)- and (3R)-β- cryptoxanthin

Khachik, Frederick,Chang, An-Ni

, p. 509 - 516 (2011/04/16)

(3S)- and (3R)-3-Hydroxy-β-ionone and (3S)- and (3R)-3-Hydroxy-β- ionone synthesized in high enantiomeric purity from commercially available () - ionone. These ionones were then transformed into (3R) - cryptoxanthin and (3S) - cryptoxanthin by a C15+C10+C15 Wittig coupling strategy according to known methods. This methodology can considerably simplify the total synthesis of optically active carotenoids with 3-hydroxy - end groups that possess significant biological activities. Georg Thieme Verlag Stuttgart New York.

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