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642-96-6

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642-96-6 Usage

Physical state

White, crystalline solid

Photography

Developer for black and white film

Industrial processes

Reducing agent and antioxidant

Skincare products

Skin-lightening and bleaching properties

Restrictions

Use is limited in some countries due to potential toxicity and carcinogenicity

Toxicity

Can be toxic in high concentrations

Skin and eye irritation

Potential harm to the skin and eyes

Respiratory system

Potential harm to the respiratory system

Potential concerns

Carcinogenicity (cancer-causing properties) and toxicity are major concerns associated with 1,2,3,4-Benzenetetrol.

Check Digit Verification of cas no

The CAS Registry Mumber 642-96-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 642-96:
(5*6)+(4*4)+(3*2)+(2*9)+(1*6)=76
76 % 10 = 6
So 642-96-6 is a valid CAS Registry Number.

642-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzene-1,2,3,4-tetrol

1.2 Other means of identification

Product number -
Other names 1,2,3,4-tetrahydroxybenzene

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:642-96-6 SDS

642-96-6Relevant articles and documents

Synthesis of 1,2,3,4-tetrahydroxybenzenes from biomass-derived carbon

-

, (2008/06/13)

A bioengineered synthesis scheme for the production of 1,2,3,4-tetrahydroxybenzene from a carbon source is provided. Methods of producing 1,2,3,4-tetrahydroxybenzene acid from a carbon source based on the synthesis scheme are also provided. Methods are also provided for converting 1,2,3,4-tetrahydroxybenzene to 1,2,3-trihydroxybenzene by catalytic hydrogenation.

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