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115440-09-0

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115440-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115440-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,4,4 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115440-09:
(8*1)+(7*1)+(6*5)+(5*4)+(4*4)+(3*0)+(2*0)+(1*9)=90
90 % 10 = 0
So 115440-09-0 is a valid CAS Registry Number.

115440-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-phenylhydrazinyl)naphthalene-2,6-dione

1.2 Other means of identification

Product number -
Other names 1-phenylazo-naphthalene-2,6-diol

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:115440-09-0 SDS

115440-09-0Downstream Products

115440-09-0Relevant articles and documents

Cytochrome P-450 from Tulip Bulbs (Tulipa fosteriana l.) oxidizes an azo dye sudan I (1-Phenylazo-2-Hydroxynaphthalene, solvent yellow 14) in vitro

Stiborova, Marie,Hansikova, Hana

, p. 1689 - 1696 (2007/10/03)

The microsomal fraction from tulip bulbs (Tulipa fosteriana L.) contains cytochrome P-450 enzymes catalyzing the NADPH-dependent oxidation of the xenobiotic substrate, an azo dye Sudan I (1-phenylazo-2-hydroxynaphthalene, Solvent Yellow 14). C-Hydroxy derivatives [1-(4-hydroxyphenylazo)-2-hydroxynaphthalene, 1-phenylazo-2,6-dihydroxynaphthalene, 1-(4-hydroxyphenylazo)-2,6-dihydroxynaphthalene] and the benzenediazonium ion are the products of the Sudan I oxidation. The oxidation of Sudan I has also been assessed in a reconstituted electron-transport chain with the isolated cytochrome P-450, isolated plant NADPH-cytochrome P-450 reductase and phospholipid. The results are discussed from the point of view of the role of cytochromes P-450 in the metabolism of xenobiotics in plants.

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