Phenol, 3-(ethylamino)-

Min.Order / FOB Price:Get Latest Price

1 Kilogram	Negotiable

1 Kilogram

Negotiable

Min.Order :1 Kilogram
Purity: 99%
Payment Terms : L/C,T/T,Other

Keywords

Phenol, 3-(ethylamino)-? price Phenol, 3-(ethylamino)-? CAS 621-31-8 Phenol, 3-(ethylamino)-? supplier in China

Quick Details

Appearance:Very viscous deep orange liquid.
Application:Used to make other chemicals.
PackAge:1kg/bag, 1kg/drum or 25kg/drum or as per your request.
ProductionCapacity:1|Metric Ton|Month
Storage:Stored in cool, dry and ventilation place; Away from fire and heat
Transportation:as per your request

Superiority:

superior quality moderate price & quick delivery

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Safety Information

Risk Statements	34
Safety Statements	26-36/37/39
RIDADR	1759

MSDS Information

3-ETHYLAMINOPHENOL Usage And Synthesis

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.