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3-ACETAMIDOPHENOL

3-ACETAMIDOPHENOL Suppliers list
Company Name: TargetMol Chemicals Inc.  Gold
Tel: 4008200310 15002144251
Email: marketing@tsbiochem.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com

3-ACETAMIDOPHENOL manufacturers

  • Metacetamol
  • Metacetamol pictures
  • $29.00
  • 2026-09-10
  • CAS:621-42-1
  • Purity: 99.76%
  • Supply Ability: 10g
  • Metacetamol
  • Metacetamol pictures
  • $29.00
  • 2026-08-08
  • CAS:621-42-1
  • Purity: 99.76%
  • Supply Ability: 10g
  • Metacetamol
  • Metacetamol pictures
  • $29.00
  • 2025-04-28
  • CAS:621-42-1
  • Purity: 99.90%
  • Supply Ability: 10g
3-ACETAMIDOPHENOL Basic information
Preparation
Product Name:3-ACETAMIDOPHENOL
Synonyms:3-(Acetylamino)-1-hydroxybenzene;3-(Acetylamino)phenol;3’-hydroxy-acetanilid;3-Hydroxy-4-trimethylammoniobutanoate3'-hydroxyacetanilide;Acetamide, N-(3-hydroxyphenyl)-;Acetanilide, 3'-hydroxy-;BS 479;BS 749
CAS:621-42-1
MF:C8H9NO2
MW:151.16
EINECS:210-687-0
Product Categories:Aromatic Phenols;Phenol&Thiophenol&Mercaptan;Anilines, Amides & Amines;Phenols
Mol File:621-42-1.mol
3-ACETAMIDOPHENOL Structure
3-ACETAMIDOPHENOL Chemical Properties
Melting point 145-148 °C(lit.)
Boiling point 273.17°C (rough estimate)
density 1.249
refractive index 1.5810 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform (Slightly), DMSO (Slightly), Methanol
pka9.50±0.10(Predicted)
form Crystals, Crystalline Powder or Needles
color Off-white to tan or light gray
PH6-7 (H2O)(saturated solution)
BRN 907998
InChI1S/C8H9NO2/c1-6(10)9-7-3-2-4-8(11)5-7/h2-5,11H,1H3,(H,9,10)
InChIKeyQLNWXBAGRTUKKI-UHFFFAOYSA-N
SMILESCC(=O)Nc1cccc(O)c1
CAS DataBase Reference621-42-1(CAS DataBase Reference)
EPA Substance Registry System3'-Hydroxyacetanilide (621-42-1)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38
Safety Statements 26-36
RIDADR 2811
WGK Germany 2
RTECS AE4100000
1-8
Hazard Note Irritant
TSCA TSCA listed
HazardClass 6.1(b)
PackingGroup III
HS Code 29242995
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
ToxicityLD50 intraperitoneal in mouse: 1025mg/kg
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
3-ACETAMIDOPHENOL Usage And Synthesis
PreparationIt can be obtained by acetylation, alkylation, hydrolysis, and neutralization of m-aminophenol.
Chemical Propertiesoff-white to tan or light grey crystals,
Uses3-Acetamidophenol is the ortho-regioisomer of Acetaminophen (A161220), an over-the-counter analgesic and antipyretic agent (1,2).
DefinitionChEBI: A derivative of phenol which has an acetamido substituent located meta to the phenolic -OH group. It is a non-toxic regioisomer of paracetamol with analgesic properties, but has never been marketed as a drug.
General DescriptionLight gray solid.
Air & Water ReactionsWater insoluble.
Reactivity ProfilePhenols 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 HazardFlash point data for 3-ACETAMIDOPHENOL are not available. 3-ACETAMIDOPHENOL is probably combustible.
Purification MethodsRecrystallise the phenol from water. The 3,5-dinitrobenzamide complex gives orange-yellow crystals from hot H2O and has m 212o. [Beilstein 13 H 415, 13 I 132, 13 II 213, 13 III 950, 13 IV 977.]
Tag:3-ACETAMIDOPHENOL(621-42-1) Related Product Information
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