ChemicalBook > Product Catalog >Organic Chemistry >Alcohols,Phenols,Phenol alcohols >Phenol derivatives >3-ETHYLAMINOPHENOL

3-ETHYLAMINOPHENOL

3-ETHYLAMINOPHENOL Structure
CAS No.
621-31-8
Chemical Name:
3-ETHYLAMINOPHENOL
Synonyms
3-(ethylamino)phenol;m-(ethylamino)phenol;m-(ethylamino)-pheno;3-(ethylamino)-pheno;Phenol, 3-(ethylamino)-;3-Hydroxyphenylethylamine
CBNumber:
CB5501890
Molecular Formula:
C8H11NO
Molecular Weight:
137.18
MOL File:
621-31-8.mol
Modify Date:
2023/5/4 15:15:15

3-ETHYLAMINOPHENOL Properties

Melting point 62°C
Boiling point 252.03°C (rough estimate)
Density 1.0630 (rough estimate)
refractive index 1.5560 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka 10.36±0.10(Predicted)
color Light Brown to Very Dark Red
EPA Substance Registry System 3-(Ethylamino)phenol (621-31-8)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H412
Precautionary statements  P264-P270-P301+P312-P330-P501-P273-P501
Risk Statements  34
Safety Statements  26-36/37/39
RIDADR  1759
HS Code  2922290090

3-ETHYLAMINOPHENOL Chemical Properties,Uses,Production

General Description

Very viscous deep orange liquid.

Air & Water Reactions

3-ETHYLAMINOPHENOL may be sensitive to prolonged exposure to air. . Slightly soluble in water.

Reactivity Profile

An amine and phenol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Phenols do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid.

Fire Hazard

Flash point data for 3-ETHYLAMINOPHENOL are not available, however, 3-ETHYLAMINOPHENOL is probably combustible.

3-ETHYLAMINOPHENOL Preparation Products And Raw materials

Global( 27)Suppliers
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SUMUKHA LIFESCIENCES +919000487488 Hyderabad, India 200 58 Inquiry
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Shanghai Daken Advanced Materials Co.,Ltd +86-371-66670886 China 16220 58 Inquiry
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Kangyue Huilan Pharmaceutical Technology Co., Ltd 028-81092800 17323275954 China 511 58 Inquiry
Henan Fangding Technology Co., LTD 15670369782 15670369782 China 9838 58 Inquiry

3-ETHYLAMINOPHENOL Spectrum

3-(ethylamino)-pheno m-(ethylamino)-pheno m-(ethylamino)phenol 3-Hydroxyphenylethylamine Phenol, 3-(ethylamino)- 3-(ethylamino)phenol 621-31-8