Product Details
Product Name:
2-sec-Butylphenol |
CAS No.:
89-72-5 |
Min. Order:
1G |
Purity:
98% |
Supply Ability:
100KG |
Release date:
2019/07/06 |
AD68
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 Chemical Properties |
Melting point |
12 °C(lit.) |
Boiling point |
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) |
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 |
TSCA |
Yes |
HazardClass |
8 |
PackingGroup |
III |
2-sec-Butylphenol Usage And Synthesis |
Chemical Properties |
colourless to light yellow liquid |
Definition |
ChEBI: A member of the class of phenols that is phenol carrying a butan-2-yl group at position 2. |
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. |
Company Profile Introduction
Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals.
Mainly deals in the sales of:
Pharmaceutical intermediates
OLED intermediates:
Pharmaceutical intermediates;
OLED intermediates;
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