2-sec-Butylphenol

2-sec-Butylphenol

2-sec-Butylphenol

Min.Order / FOB Price:Get Latest Price

1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 99.0%
  • Payment Terms : L/C,D/A,D/P,T/T,,MoneyGram,Other

Keywords

89-72-5 2-sec-Butylphenol 2-sec-Butylphenol

Quick Details

  • Appearance:colourless to light yellow liquid
  • Application:For Organic Synthesis use
  • PackAge:IN 25kg drums
  • ProductionCapacity:10|Metric Ton|Month
  • Storage:In Room Temperature
  • Transportation: As Per MSDS

Superiority:

2-sec-Butylphenol Basic information
Product Name: 2-sec-Butylphenol
Synonyms: OSBP;O-S-BUTYLPHENOL;O-SEC-BUTYLPHENOL;ORTHO-SEC-BUTYLPHENOL;2-SEC-BUTYLPHENOL;1-(1-Methylpropyl)phenol;2-(1-methylpropyl)-pheno;2-(1-Methylpropyl)phenol
CAS: 89-72-5
MF: C10H14O
MW: 150.22
EINECS: 201-933-8
Product Categories: Organic Building Blocks;Oxygen Compounds;Phenols
Mol File: 89-72-5.mol
2-sec-Butylphenol Structure

 

Details:

 
 
2-sec-Butylphenol Chemical Properties
mp  12 °C(lit.)
bp  226-228 °C(lit.)
density  0.982 g/mL at 25 °C(lit.)
vapor pressure  0.03 mm Hg ( 20 °C)
refractive index  n20/D 1.522(lit.)
Fp  234 °F
Water Solubility  Insoluble. <0.1 g/100 mL at 20 ºC
BRN  1210026
Stability: Stable, but air sensitive. Incompatible with acid chlorides, acid anhydrides, bases, strong oxidizing agents, copper and its alloys, brass.
CAS DataBase Reference 89-72-5(CAS DataBase Reference)
NIST Chemistry Reference Phenol, 2-(1-methylpropyl)-(89-72-5)
EPA Substance Registry System Phenol, 2-(1-methylpropyl)-(89-72-5)
 
Safety Information
Hazard Codes  C
Risk Statements  20/21/22-34-22
Safety Statements  26-27-28-36/37/39-45
RIDADR  UN 3145 8/PG 2
WGK Germany  2
RTECS  SJ8920000
HazardClass  8
PackingGroup  III
 
 
2-sec-Butylphenol Usage And Synthesis
Chemical Properties colourless to light yellow liquid
General Description Clear colorless liquid.
Air & Water Reactions Insoluble in water.
Reactivity Profile Phenols, such as 2-sec-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 2-sec-Butylphenol is combustible.
 
2-sec-Butylphenol Preparation Products And Raw materials
Preparation Products Fenobucarb

 

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