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2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-[(4-chlorophenyl)azo]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109480-39-9

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109480-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109480-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,8 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 109480-39:
(8*1)+(7*0)+(6*9)+(5*4)+(4*8)+(3*0)+(2*3)+(1*9)=129
129 % 10 = 9
So 109480-39-9 is a valid CAS Registry Number.

109480-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(4-chlorophenyl)diazenyl]-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 2,4,6(1H,3H,5H)-Pyrimidinetrione,5-[(4-chlorophenyl)azo]

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:109480-39-9 SDS

109480-39-9Downstream Products

109480-39-9Relevant academic research and scientific papers

Monoazo yellow organic pigment and preparation method thereof

-

Paragraph 0038-0048, (2021/02/06)

The invention discloses a monoazo yellow organic pigment as shown in a formula I. R1 and R2 are respectively and independently selected from H, OH, NO2, Cl, Br and C1-C4 alkyl, and m is a positive integer from 1 to 3, n is a positive integer from 1 to 3; Ar is that no sodium chloride or sodium hydrogen sulfate/sodium sulfate is generated in the process of preparing the monoazo yellow organic pigment, and the yield is higher than 96%.

Dissociation constants of substituted aryl azo barbituric and thiobarbituric acids

Masoud, Mamdouh S.,Ghonaim, Ahmed K.,Ahmed, Rabah H.,Mahmoud, Ahmed A.,Ali, Alaa E.

, p. 531 - 542 (2007/10/03)

The acid dissociation constants of 5-(substituted phenylazo) barbituric and thiobarbituric acids were determined in aqueous media and in 25%-75% (v/v) ethanol-water and dioxanewater mixtures potentiometrically in the temperature range 25-40°C, in presence

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