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3-amino-2,6-xylenol, also known as 3-methyl-4-amino-phenol, is a chemical compound with the molecular formula C8H11NO. It is a derivative of xylenol, an aromatic compound, featuring an amino group and a hydroxyl group attached to the benzene ring. 3-amino-2,6-xylenol is known for its role as a colorant and antioxidant in hair dyes and hair care products, as well as its utility in the synthesis of pharmaceutical compounds and as a common reagent in organic chemistry laboratories. Despite its low acute toxicity, caution is advised against prolonged exposure.

6994-64-5

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6994-64-5 Usage

Uses

Used in Hair Dye and Hair Care Products:
3-amino-2,6-xylenol is used as a colorant and antioxidant in hair dyes and hair care products for its ability to act as a reducing agent, which helps maintain the stability and color of the hair dye.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 3-amino-2,6-xylenol is used as a key intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new medications.
Used in Organic Chemistry Laboratories:
As a common reagent in organic chemistry, 3-amino-2,6-xylenol is utilized in a variety of laboratory applications, including as a starting material for the synthesis of various organic compounds and for educational purposes in teaching the principles of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 6994-64-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,9 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6994-64:
(6*6)+(5*9)+(4*9)+(3*4)+(2*6)+(1*4)=145
145 % 10 = 5
So 6994-64-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO/c1-5-3-4-7(9)6(2)8(5)10/h3-4,10H,9H2,1-2H3

6994-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-2,6-dimethylphenol

1.2 Other means of identification

Product number -
Other names 3-Amino-2,6-xylenol

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:6994-64-5 SDS

6994-64-5Relevant academic research and scientific papers

BROMODOMAIN INHIBITORS

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Paragraph 00483, (2017/11/10)

The present invention provides for compounds of formula (I) wherein R1, R2, R3, R4, R6, X1, and X2 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions, including inflammatory diseases, cancer, and AIDS. Also provided are pharmaceutical compositions comprising compounds of formula (I).

New evidence against hydroxyl radicals as reactive intermediates in the thermal and photochemically enhanced fenton reactions

Bossmann, Stefan H.,Oliveros, Esther,Goeb, Sabine,Siegwart, Silvia,Dahlen, Elizabeth P.,Payawan Jr., Leon,Straub, Matthias,Woerner, Michael,Braun, Andre M.

, p. 5542 - 5550 (2007/10/03)

During the oxidative degradation of 2,4-dimethylaniline (2,4-xylidine) by means of the H2O2/UV method, a series of hydroxylated aromatic amines are formed, this result confirming the role of the hydroxyl radical as an initiator of the oxidative chain reaction. Thermal or photochemically enhanced Fenton reactions in the presence of 2,4-dimethylaniline (2,4-xylidine) yield primarily 2,4-dimethylphenol as an intermediate product, the genesis of which may only be explained by an electron transfer mechanism. Experimental evidence for such a mechanism is presented, and values for the quantum yields of the photochemically enhanced reduction of iron(III) to iron(II) in aqueous solutions of 2,4-xylidine are given.

Substituted ortho-aminophenols, process for preparing them and their use for the oxidatin dyeing of keratinous fibres

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, (2008/06/13)

5-Substituted ortho-aminophenols of formula: STR1 in which: R1 denotes a hydrogen atom, an alkyl radical having 1 to 4 carbon atoms or a hydroxyalkyl radical having 1 to 4 carbon atoms; and R2 denotes, independently of R1, an alkyl radical having 1 to 4 carbon atoms, an alkoxy radical having 1 to 4 carbon atoms or a benzyl radical; the addition salts with an acid and the phenates, and dyeing composition containing a compound of formula (I) or a salt or a phenate of such a compound. The 5-substituted ortho-aminophenols enable hair to be dyed in a rich spectrum of hues having good durability.

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