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35975-12-3

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35975-12-3 Usage

Description

3,6-Dimethyl-1,2-benzendiamine, also known as 3,6-Dimethyl-o-phenylenediamine, is an organic compound belonging to the benzendiamine class. It is characterized by its ability to produce vibrant and long-lasting colors, making it a valuable component in the formulation of various dyes.

Uses

Used in Hair Dye Industry:
3,6-Dimethyl-1,2-benzendiamine is used as a key ingredient in hair dyes for its capacity to create vibrant and long-lasting colors. It contributes to the effectiveness and quality of hair coloring products, enhancing their performance and consumer satisfaction.
Used in Textile Industry:
In the textile industry, 3,6-Dimethyl-1,2-benzendiamine is utilized as a dye component to impart color to fabrics. Its properties allow for the creation of a wide range of hues, adding aesthetic value and visual appeal to textile products.

Check Digit Verification of cas no

The CAS Registry Mumber 35975-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,7 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35975-12:
(7*3)+(6*5)+(5*9)+(4*7)+(3*5)+(2*1)+(1*2)=143
143 % 10 = 3
So 35975-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-5-3-4-6(2)8(10)7(5)9/h3-4H,9-10H2,1-2H3

35975-12-3SDS

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 3,6-dimethylbenzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names 3,6-DIMETHYL-1,2-BENZENDIAMINE

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:35975-12-3 SDS

35975-12-3Relevant articles and documents

Mechanism-Inspired Design of Bifunctional Catalysts for the Alternating Ring-Opening Copolymerization of Epoxides and Cyclic Anhydrides

Abel, Brooks A.,Lidston, Claire A. L.,Coates, Geoffrey W.

supporting information, p. 12760 - 12769 (2019/08/26)

Advances in catalysis have enabled the ring-opening copolymerization of epoxides and cyclic anhydrides to afford structurally and functionally diverse polyesters with controlled molecular weights and dispersities. However, the most common systems employ b

Asymmetric Hydrogenation of 3,5-Bistrifluoromethyl Acetophenone in Pilot Scale with Industrially Viable Ru/Diphosphine-Benzimidazole Complexes

Xu, Liang,Huang, Zhi-Hong,Sandoval, Christian A.,Gu, Lian-Quan,Huang, Zhi-Shu

, p. 1137 - 1141 (2015/04/22)

A novel efficient asymmetric hydrogenation (AH) process was developed for the preparation of (R)-1-(3,5-bis(trifluoromethyl)phenyl)ethanol (3), using a catalyst Ru/(4R,5R)-(+)-4,5-bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxoane-(R,R-Diop)-2R-(α-met

Catalysts and process for producing aromatic amines

-

, (2008/06/13)

As catalysts for producing aromatic amines by hydrogenating aromatic nitrites, there are disclosed (1) the catalyst comprising a metal catalyst component comprising Ni and/or Co and a specific amount of zirconia as a carrier component, which is prepared b

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