CasNo.621-42-1,621-42-1 C8H9NO2 3-ACETAMIDOPHENOL,(621-42-1) Suppliers

1 Metric Ton	Negotiable

Min.Order :1 Metric Ton
Purity: 99.5%
Payment Terms : L/C,T/T,

Keywords

3-ACETAMIDOPHENOL 621-42-1 C8H9NO2

Quick Details

Appearance:Powder
Application:621-42-1
PackAge:Aluminium Foil Bag and Paper Drum
ProductionCapacity:1|Metric Ton|Day
Storage:1MT
Transportation:By Sea/Air/DHL

Superiority:

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1.Noble Metal Catalysts (Pt.Pd...)

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3.OLED intermediates (Fluorene,Carbazole,Boric acid...)

4.Customs Synthesis

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Details:

3-ACETAMIDOPHENOL Basic information

Product Name:	3-ACETAMIDOPHENOL
Synonyms:	N-(3-HYDROXYPHENYL)ACETAMIDE;M-HYDROXYACETANILIDE;3-(Acetylamino)-1-hydroxybenzene;3-(Acetylamino)phenol;3’-hydroxy-acetanilid;3-Hydroxy-4-trimethylammoniobutanoate3'-hydroxyacetanilide;Acetamide, N-(3-hydroxyphenyl)-;Acetanilide, 3'-hydroxy-
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 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.	2-8°C
form	Crystals, Crystalline Powder or Needles
color	Off-white to tan or light gray
PH	6-7 (H2O)(saturated solution)
BRN	907998
CAS DataBase Reference	621-42-1(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi,Xn
Risk Statements	36/37/38
Safety Statements	26-36
RIDADR	2811
WGK Germany	2
RTECS	AE4100000
F	1-8
Hazard Note	Irritant
TSCA	Yes
HazardClass	6.1(b)
PackingGroup	III
HS Code	29242995

MSDS Information

Provider	Language
SigmaAldrich	English
ACROS	English
ALFA	English

3-ACETAMIDOPHENOL Usage And Synthesis

Chemical Properties	off-white to tan or light grey crystals,
Uses	analgesic
Definition	ChEBI: 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 Description	Light gray solid.
Air & Water Reactions	Water insoluble.
Reactivity Profile	Phenols 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 3-ACETAMIDOPHENOL are not available. 3-ACETAMIDOPHENOL is probably combustible.