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130793-26-9

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130793-26-9 Usage

General Description

The chemical compound "(6R)-3-hexyl-3,4,5,6-tetrahydro-4-hydroxy-6-undecyl-2H-pyran-2-one" is a type of pyranone, a class of organic compounds. It has a molecular structure consisting of a six-membered ring with oxygen and carbon atoms, along with hexyl and undecyl side chains. The compound also contains a hydroxy group, which is a functional group consisting of an oxygen atom bonded to a hydrogen atom. This chemical may have potential applications in various industries, including pharmaceuticals, flavors and fragrances, and agrochemicals, due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 130793-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,7,9 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130793-26:
(8*1)+(7*3)+(6*0)+(5*7)+(4*9)+(3*3)+(2*2)+(1*6)=119
119 % 10 = 9
So 130793-26-9 is a valid CAS Registry Number.

130793-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4R,6S)-3-Hexyl-3,4,5,6-tetrahydro-4-hydroxy-6-undecyl-2H-pyran-2-one

1.2 Other means of identification

Product number -
Other names -

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:130793-26-9 SDS

130793-26-9Relevant articles and documents

Tetrahydrolipstatin: Thermal and hydrolytic degradation

Stalder,Schneider,Oesterhelt

, p. 1022 - 1036 (2007/10/02)

The thermal and hydrolytic degradation of tetrahydrolipstatin (THL, 1) was investigated. All main degradation products were isolated, characterized, and synthesized. Labile intermediates unavailable to isolation were detected and identified by GC/MS analysis of their silylated derivatives, and whenever possible, compared with independently prepared reference compounds. The identified degradation products represent at least 97% of the total degradation mixture. Two main reaction pathways are proposed. Pharmacological data are reported for the degradation mixture and the main degradation products.

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