ChemicalBook > CAS DataBase List > Phenol, 3-(dimethylamino)-4-methyl-

Phenol, 3-(dimethylamino)-4-methyl-

Product Name
Phenol, 3-(dimethylamino)-4-methyl-
CAS No.
119-31-3
Chemical Name
Phenol, 3-(dimethylamino)-4-methyl-
Synonyms
NSC7199;p-Cresol, 3-(dimethylamino)-;2-Dimethylamino-4-hydroxytoluene;3-(dimethylamino)-4-methylphenol;Phenol, 3-(dimethylamino)-4-methyl-
CBNumber
CB31214494
Molecular Formula
C9H13NO
Formula Weight
151.21
MOL File
119-31-3.mol
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Phenol, 3-(dimethylamino)-4-methyl- Property

storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
EPA Substance Registry System
3-(Dimethylamino)-4-methylphenol (119-31-3)
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Safety

HazardClass 
IRRITANT
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
D495258
Product name
3-(Dimethylamino)-4-methylphenol
Packaging
10mg
Price
$60
Updated
2021/12/16
Biosynth Carbosynth
Product number
FD120168
Product name
3-(Dimethylamino)-4-methylphenol
Packaging
50mg
Price
$60
Updated
2021/12/16
Matrix Scientific
Product number
061114
Product name
3-(Dimethylamino)-4-methylphenol
Packaging
1g
Price
$180
Updated
2021/12/16
Biosynth Carbosynth
Product number
FD120168
Product name
3-(Dimethylamino)-4-methylphenol
Packaging
250mg
Price
$200
Updated
2021/12/16
Activate Scientific
Product number
AS146200
Product name
3-(Dimethylamino)-4-methylphenol
Purity
95%
Packaging
1g
Price
$237
Updated
2021/12/16
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Phenol, 3-(dimethylamino)-4-methyl- Chemical Properties,Usage,Production

General Description

Red liquid with phenolic odor.

Air & Water Reactions

Moderately soluble in water.

Reactivity Profile

Phenols, such as Phenol, 3-(dimethylamino)-4-methyl-, 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.

Fire Hazard

Flash point data for Phenol, 3-(dimethylamino)-4-methyl- are not available. Phenol, 3-(dimethylamino)-4-methyl- is probably combustible.

Phenol, 3-(dimethylamino)-4-methyl- Preparation Products And Raw materials

Raw materials

Preparation Products

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Phenol, 3-(dimethylamino)-4-methyl- Suppliers

Carbosynth
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6005
Advantage
58

119-31-3, Phenol, 3-(dimethylamino)-4-methyl-Related Search:


  • Phenol, 3-(dimethylamino)-4-methyl-
  • NSC7199
  • 3-(dimethylamino)-4-methylphenol
  • 2-Dimethylamino-4-hydroxytoluene
  • p-Cresol, 3-(dimethylamino)-
  • 119-31-3