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ChemicalBook >> CAS DataBase List >> 4-tert-Butylphenol


CAS No.98-54-4
Chemical Name:4-tert-Butylphenol
Synonyms:PTBP;FEMA 3918;BUTYLPHEN;Lowinox 070;Lowinox PTBT;t-Butylphenol;4-tert.-Butylp;P-T-BUTYLPHENOL;4-t-Butylphenol;p-terc.Butylfenol
Molecular Formula:C10H14O
Formula Weight:150.22
MOL File:98-54-4.mol
4-tert-Butylphenol Property
Melting point : 96-101 °C(lit.)
Boiling point : 236-238 °C(lit.)
density : 0.908 g/mL at 25 °C(lit.)
vapor pressure : 1 mm Hg ( 70 °C)
FEMA : 3918
refractive index : 1.4787
Fp : 113 °C
Water Solubility : 8.7 g/L (20 ºC)
Merck : 14,1585
BRN : 1817334
Stability:: Stable. Incompatible with copper, steel, bases, acid chlorides, acid anhydrides, oxidizing agents.
CAS DataBase Reference: 98-54-4(CAS DataBase Reference)
NIST Chemistry Reference: Phenol, p-tert-butyl-(98-54-4)
Hazard Codes : Xi,N
Risk Statements : 37/38-41-51/53-62-38-37
Safety Statements : 26-39-61-36/37/39
RIDADR : UN 3077 9/PG 3
WGK Germany : 2
RTECS : SJ8925000
HazardClass : 8
PackingGroup : III
HS Code : 29071900

4-tert-Butylphenol Chemical Properties,Usage,Production

Chemical Properties
white crystalline powder
ChEBI: A member of the class of phenols that is phenol substituted with a tert-butyl group at position 4..
General Description
Crystals or practically white flakes. Has a disinfectant-like odor. May float or sink in water. Insoluble in water.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Phenols, such as 4-tert-Butylphenol, 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
4-tert-Butylphenol Preparation Products And Raw materials
Raw materials
4-N-OCTYLPHENOL 2,6-DTBP Phenol AMBERLITE(R) IRC-50 ISOBUTYLENE tert-Butanol Aluminium chloride p-Tert-butylphenol POLYISOBUTYLENE Benzoic acid 2,4,4-TRIMETHYL-2-PENTENE
Preparation Products
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