| Identification | Back Directory | [Name]
Phenol, 3-(dimethylamino)-4-methyl- | [CAS]
119-31-3 | [Synonyms]
NSC7199
p-Cresol, 3-(dimethylamino)-
3-(dimethylamino)-4-methylphenol
2-Dimethylamino-4-hydroxytoluene
Phenol, 3-(dimethylamino)-4-methyl- | [Molecular Formula]
C9H13NO | [MDL Number]
MFCD08361738 | [MOL File]
119-31-3.mol | [Molecular Weight]
151.21 |
| Hazard Information | Back Directory | [General Description]
Red liquid with phenolic odor. | [Air & Water Reactions]
Moderately soluble in water. | [Reactivity Profile]
Phenols, such as Phenol, 3-(dimethylamino)-4-methyl-(119-31-3), 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. |
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