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65235-31-6

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65235-31-6 Usage

Contact allergens

This dye belongs to the aminophenol class and is used as a hair colorant, particularly in semipermanent hair dye preparations.

Check Digit Verification of cas no

The CAS Registry Mumber 65235-31-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,3 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65235-31:
(7*6)+(6*5)+(5*2)+(4*3)+(3*5)+(2*3)+(1*1)=116
116 % 10 = 6
So 65235-31-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O4/c11-4-3-9-7-2-1-6(12)5-8(7)10(13)14/h1-2,5,9,11-12H,3-4H2

65235-31-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-Hydroxyethylamino)-3-Nitrophenol

1.2 Other means of identification

Product number -
Other names 4-(2-hydroxyethylamino)-3-nitrophenol

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:65235-31-6 SDS

65235-31-6Synthetic route

2-nitro-N-hydroxyethyl-p-anisidine
57524-53-5

2-nitro-N-hydroxyethyl-p-anisidine

4-[(2'-hydroxyethyl)amino]-3-nitrophenol
65235-31-6

4-[(2'-hydroxyethyl)amino]-3-nitrophenol

Conditions
ConditionsYield
With hydrogen bromide Reflux;93%

65235-31-6Relevant articles and documents

Synthesis method of 3-nitro-4-hydroxyethylaminophenol

-

Paragraph 0022; 0025-0027; 0030-0031; 0034, (2020/07/12)

The invention relates to a synthesis method of 3-nitro-4-hydroxyethylaminophenol. The method comprises the following steps: reacting a compound shown as a formula I with ethanolamine under a heating condition to obtain a compound shown as formula II; and (2) heating the compound II obtained in the step (1) and hydrobromic acid to a reflux condition, carrying out demethylation reaction to obtain acompound 3-nitro-4-hydroxyethylaminophenol hydrobromide, and carrying out reaction on the compound 3-nitro-4-hydroxyethylaminophenol hydrobromide and concentrated ammonia water to obtain a compound shown as formula III, i.e. a target product. The invention provides a brand-new reaction route, cheap and easily available 4-dimethoxy-2-nitrobenzene and ethanolamine are used as the main raw materials,the whole preparation process is simple, easy to operate and free of high toxicity and high risk, the yield of the obtained product is high, and industrial production is easy to realize; and the rawmaterials ethanolamine and hydrobromic acid in the reaction process can both be recycled, thereby reducing three wastes and saving the cost.

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