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Benzenemethanol, 2-hydroxy-5-[(4-nitrophenyl)azo]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

155850-91-2

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155850-91-2 Usage

Usage

Synthetic azo dye
Textile industry
Food industry (used to impart red color to products like curry powder, chili powder, and paprika)

Health Risks

Potential carcinogen
Banned as a food additive in several countries
Linked to increased risk of bladder cancer and liver tumors in animal studies

Check Digit Verification of cas no

The CAS Registry Mumber 155850-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,5 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155850-91:
(8*1)+(7*5)+(6*5)+(5*8)+(4*5)+(3*0)+(2*9)+(1*1)=152
152 % 10 = 2
So 155850-91-2 is a valid CAS Registry Number.

155850-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(hydroxymethyl)-4-[(4-nitrophenyl)hydrazinylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names Benzenemethanol,2-hydroxy-5-[(4-nitrophenyl)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:155850-91-2 SDS

155850-91-2Relevant academic research and scientific papers

Colorimetric detection of cyanide with a chromogenic oxazine

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Page/Page column 2; 4; 8, (2009/10/21)

A chromogenic oxazine compound for the colorimetric detection of cyanide was designed. Indeed, the [1,3]oxazine ring of our compound opens to form a phenolate chromophore in response to cyanide. The heterocyclic com-pound may be comprised of fused benzoox

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