2-Acetamido-4-methy...

2-Acetamido-4-methylphenol
2-Acetamido-4-methylphenol
2-Acetamido-4-methylphenol

2-Acetamido-4-methylphenol

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100 Gram

Negotiable

  • Min.Order :100 Gram
  • Purity: 99%
  • Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

2-ACETAMIDO-P-CRESOL HIGH purity by own lab 6375-17-3 N1-(2-HYDROXY-5-METHYLPHENYL)ACETAMIDE

Quick Details

  • Appearance: white to brown low melting crystalline solid
  • Application:6375-17-3
  • PackAge:1g;5g;10g;25g;50g;100g;500g;1KG;5KG,25kg,50kg or as customers request
  • ProductionCapacity:100|Kilogram|Month
  • Storage:2-8, cold storage, to avoid light storage.
  • Transportation:BY SEA /BY AIR /BY COURIER

Superiority:

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-Hydroxy-5-Methylacetaniline;2-ACETAMIDO-P-CRESOL
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 Structure
 
2-Acetamido-4-methylphenol Chemical Properties
mp  151 °C
CAS DataBase Reference 6375-17-3(CAS DataBase Reference)
EPA Substance Registry System Acetamide, N-(2-hydroxy-5-methylphenyl)-(6375-17-3)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39-36
MSDS Information
Provider Language
2-Acetamido-4-methylphenol English
ALFA English
 
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.

 

 

 

 

 

 

 

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