3-butylphenol

3-butylphenol Suppliers list
Company Name: Hangzhou MolCore BioPharmatech Co.,Ltd.
Tel: +86-057181025280; +8617767106207
Email: sales@molcore.com
Products Intro: Product Name:3-Butylphenol
CAS:4074-43-5
Purity:NLT 98% Remarks:MC808936
Company Name: Amadis Chemical Company Limited
Tel: 571-89925085
Email: sales@amadischem.com
Products Intro: Product Name:3-Butylphenol
CAS:4074-43-5
Purity:0.97 Package:mgs,gs,kgs Remarks:A905361
Company Name: Zhuhai Aobokai Biomedical Technology Co., Ltd.  
Tel: 400-0628126 15976997964;
Email: sales-team@aobchem.com.cn
Products Intro: Product Name:3-butylphenol
CAS:4074-43-5
Purity:95%+ Package:1g;5kg Remarks:154560
Company Name: HONEST JOY HOLDINGS LIMITED  
Tel: +86-755-26404303
Email: sales@honestjoy.cn
Products Intro:
3-butylphenol Basic information
Product Name:3-butylphenol
Synonyms:META-TERT-BUTYLPHENOL;m-Butylphenol;3-butylphenol;Phenol, 3-butyl-
CAS:4074-43-5
MF:C10H14O
MW:150.22
EINECS:223-790-0
Product Categories:
Mol File:4074-43-5.mol
3-butylphenol Structure
3-butylphenol Chemical Properties
Melting point 46.81°C (estimate)
Boiling point 247°C
density 0.9740
refractive index 1.5094 (estimate)
pka10.07±0.10(Predicted)
Safety Information
MSDS Information
3-butylphenol Usage And Synthesis
Chemical PropertiesThe butylphenols include several isomers. Solid butylphenols (28805-86-9) generally have properties similar to the above:
Potential ExposureButylphenols may be used as intermediates in manufacturing varnish and lacquer resins; as a germicidal agent in detergent disinfectants; as a pour point depressant, in motor-oil additives; de-emulsifier for oil; soap-antioxidant, plasticizer, fumigant, and insecticide
ShippingUN2430 Alkylphenols, solid, n.o.s. (including C2-C12 homologues), Hazard class: 8; Labels: 8— Corrosive material
IncompatibilitiesVapors may form explosive mixture with air. These phenol/cresol materials can react with oxidizers; reaction may be violent. 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 cause the gas to ignite and explode. Heat is also generated by the acid-base reaction with bases; such heating may initiate polymerization of the organic compound. React with boranes, alkalies, aliphatic amines, amides, nitric acid, sulfuric acid. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). These reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid and can explode when heated. Many phenols form metal salts that may be detonated by mild shock
3-butylphenol Preparation Products And Raw materials
Raw materialsPhenol, 3-(1-butenyl)- (9CI)-->3-butylcyclohex-2-enone
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