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93525-18-9

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93525-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93525-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,2 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93525-18:
(7*9)+(6*3)+(5*5)+(4*2)+(3*5)+(2*1)+(1*8)=139
139 % 10 = 9
So 93525-18-9 is a valid CAS Registry Number.

93525-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-hydroxy-6,10-dimethylundeca-5,9-dien-2-one

1.2 Other means of identification

Product number -
Other names 11-hydroxygeranylacetone

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:93525-18-9 SDS

93525-18-9Upstream product

93525-18-9Downstream Products

93525-18-9Relevant articles and documents

Utility of microbes in organic synthesis: Selective transformations of acyclic isoprenoids by Aspergillus niger

Madyastha, K M,Gururaja, T L

, p. 609 - 614 (2007/10/02)

Bioconversion of acyclic isoprenoids using a strain of Aspergillus niger results in hydroxylated metabolites with regio- and stereoselectivity.The organism carries out oxidation of the terminal allylic methyl group and the remote double bond in all the compounds tested (I-VII).However, these two activities seem to have preferential structural requirements.When an acyclic isoprenoid with a ketone functionality such as geranylacetone is used as the substrate, the organism also carries out the asymmetric reduction of the keto group.All the metabolites formed have beenpurified and characterized by conventional spectroscopic methods and quantification has been made by gas chromatographic analyses.

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