2-Acetamido-4-methylphenol
2-Acetamido-4-methylphenol Basic information
- Product Name:
- 2-Acetamido-4-methylphenol
- Synonyms:
-
- n-(2-hydroxy-5-methylphenyl)-acetamid
- N-(2-Hydroxy-5-methylphenyl)acetamide
- N1-(2-HYDROXY-5-METHYLPHENYL)ACETAMIDE
- 2-ACETOMIDO-P-CRESOL
- 2-ACETAMIDO-4-METHYLPHENOL
- 2-HYDROXY-5-METHYLACETANILIDE
- 2-acetamido-4-cresol
- 2-Acetylamino-4-methylphenol
- CAS:
- 6375-17-3
- MF:
- C9H11NO2
- MW:
- 165.19
- EINECS:
- 228-934-6
- Product Categories:
-
- Intermediates of Dyes and Pigments
- Phenol&Thiophenol&Mercaptan
- Mol File:
- 6375-17-3.mol
2-Acetamido-4-methylphenol Chemical Properties
- Melting point:
- 151 °C
- Boiling point:
- 336.5±30.0 °C(Predicted)
- Density
- 1.203±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- form
- powder to crystal
- pka
- 9.57±0.48(Predicted)
- color
- White to Light yellow
- CAS DataBase Reference
- 6375-17-3(CAS DataBase Reference)
- EPA Substance Registry System
- 2'-Hydroxy-5'-methylacetanilide (6375-17-3)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-37/39-36
- TSCA
- Yes
- HS Code
- 2924.29.7790
MSDS
- Language:English Provider:2-Acetamido-4-methylphenol
- Language:English Provider:ALFA
2-Acetamido-4-methylphenol Usage And Synthesis
Chemical Properties
needles
General Description
Solid.
Reactivity Profile
Compounds in this group 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. 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. Nitrated phenols often explode when heated. Many of them form metal salts that tend toward detonation by rather mild shock. Flammable gases are formed by the reaction of organic amides with strong reducing agents. Amides are very weak bases (weaker than water). Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).
Fire Hazard
Flash point data for 2-Acetamido-4-methylphenol are not available. 2-Acetamido-4-methylphenol is probably combustible.
2-Acetamido-4-methylphenolSupplier
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2-Acetamido-4-methylphenol(6375-17-3)Related Product Information
- Acetaminophen
- o-Cresol
- Acetamide
- p-Cresol
- CHLOROPHOSPHONAZO III
- 3-Ethylphenol
- 2-Aminophenol
- 6-Methoxy-meta-acetoluidide
- N-Acetoacetyl cresidine
- 3-HYDROXY-2-ACETYLAMINOFLUORENE
- 1-(2-METHOXY-5-METHYLPHENYL)-1H-PYRROLE-2,5-DIONE
- METHYL-3-[2-(4-AMINOBENZOYL)ACETAMINO]-4-[3,5-DICARBOXYMETHYL)-PHENOXY]-BENZOATE
- 2-CHLORO-N-(2-METHOXY-5-METHYLPHENYL)ACETAMIDE
- 2-Acetamido-4-methylphenol
- ACETAMINOPHENOL BP/USP
- METHYL-3-[2-(4-NITROBENZOYL)ACETAMINO]-4-[3,5-DICARBOXYMETHYL)-PHENOXY]-BENZOATE
- 5-[4-CARBOXY-2-[[1,3-DIOXO-3-[4-[(1-OXOOCTADECYL)-AMINO]PHENYL]PROPYL] AMINO]PHENOXY]ISOPHTHALIC ACID
- LABOTEST-BB LT00159665