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98-54-4 C10H14O 4-tert-Butylphenol

CAS NO.98-54-4

  • Min.Order: 25 Metric Ton
  • Payment Terms: L/C,D/A,D/P,T/T,
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Product Details

Keywords

  • 98-54-4 C10H14O 4-tert-Butylphenol
  • 98-54-4
  • C10H14O

Quick Details

  • ProName: 98-54-4 C10H14O ...
  • CasNo: 98-54-4
  • Molecular Formula: C10H14O
  • Appearance: white solid
  • Application: Industrial/Fine Chemicals;Aromatic Phe...
  • DeliveryTime: 5 working days after cash deposit
  • PackAge: the plastic woven bag
  • Port: depend on clients require
  • ProductionCapacity: 1 Metric Ton/Day
  • Purity: 99%
  • Storage: saty away from the water and sun
  • Transportation: by express or by sea
  • LimitNum: 25 Metric Ton

Superiority

 

 
4-tert-Butylphenol Chemical Properties
mp  96-101 °C(lit.)
bp  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)
 
Safety Information
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
MSDS Information
Provider Language
4-(1,1-Dimethylethyl)phenol English
SigmaAldrich English
ACROS English
ALFA English
 
4-tert-Butylphenol Usage And Synthesis
Chemical Properties white crystalline powder
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 Combustible.

 

Details

 

 
4-tert-Butylphenol Chemical Properties
mp  96-101 °C(lit.)
bp  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)
 
Safety Information
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
MSDS Information
Provider Language
4-(1,1-Dimethylethyl)phenol English
SigmaAldrich English
ACROS English
ALFA English
 
4-tert-Butylphenol Usage And Synthesis
Chemical Properties white crystalline powder
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 Combustible.

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