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Acetoacetanilide

CAS No.
102-01-2
Chemical Name:
Acetoacetanilide
Synonyms
AAA;3-OXO-N-PHENYLBUTANAMIDE;AAN;ethyl 3-oxo-3-(phenylamino)propanoate;Acetoacetanilid;n-phenylacetoacetamide;Linazol;usafek-1239;Coupler 633;USAF ek-1239
CBNumber:
CB0463919
Molecular Formula:
C10H11NO2
Molecular Weight:
177.2
MDL Number:
MFCD00008780
MOL File:
102-01-2.mol
MSDS File:
SDS
Last updated:2023-04-23 13:52:06

Acetoacetanilide Properties

Melting point 83-88 °C (lit.)
Boiling point 129°C 24mm
Density 1.26
vapor density 6.1 (vs air)
vapor pressure 0-0.013Pa at 20-50℃
refractive index 1.5168 (estimate)
Flash point 325 °F
storage temp. Refrigerator
solubility Chloroform (Slightly), Methanol (Slightly)
pka 12.21±0.46(Predicted)
form Crystalline Powder
color White
Water Solubility 5 g/L (20 ºC)
Merck 14,58
BRN 473419
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
LogP 0.93 at 23℃
CAS DataBase Reference 102-01-2(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII W35JB9PY3X
NIST Chemistry Reference Butanamide, 3-oxo-N-phenyl-(102-01-2)
EPA Substance Registry System Acetoacetanilide (102-01-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Warning
Hazard statements  H341-H302-H312
Precautionary statements  P280f-P280-P201-P202-P308+P313-P405-P501
Hazard Codes  Xn
Risk Statements  21/22
Safety Statements  36
RTECS  AK4200000
Autoignition Temperature 843 °F
HS Code  2921419000
Toxicity LD50 orl-rat: 5400 mg/kg LONZA# 08FEB79
NFPA 704
1
1 0

Acetoacetanilide Chemical Properties,Uses,Production

Chemical Properties

White to off-white powder

Uses

Acetoacetanilide is used as intermediate for the manufacture of organic pigments and dyestuffs.

Uses

Acetoacetanilide may be used to synthesize:

  • azo pigments
  • acetoacetanilido-4-aminoantipyrine (Schiff base)
  • 6-aryl-2-methyl-4-oxo-N,N′-diphenyl-2-cyclohexene-1,3-dicarboxamides
  • photoluminescent lanthanide complexes

Uses

Acetoacetanilide (AAA) flakes is used as an intermediate for the manufacture of organic pigments and dyestuffs. For further information consult the Product information sheet. Product Data Sheet

Synthesis Reference(s)

The Journal of Organic Chemistry, 56, p. 1713, 1991 DOI: 10.1021/jo00005a013

General Description

White crystalline solid.

Air & Water Reactions

Water insoluble.

Reactivity Profile

Organic amides react with azo and diazo compounds to generate toxic gases. 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). Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

Health Hazard

ACUTE/CHRONIC HAZARDS: Acetoacetanilide is a weak allergen. When heated to decomposition it emits toxic fumes.

Fire Hazard

Acetoacetanilide is combustible.

Safety Profile

Poison by intraperitoneal route. Moderately toxic by ingestion. A weak allergen. See also ACETANILIDE. Combustible when exposed to heat or flame. See ANILINE and CYANIDE for disaster hazard. When heated to decomposition it emits toxic NOx, fumes. To fight fire, use alcohol foam, water mist, CO2, dry chemical.

Purification Methods

Crystallise the anilide from H2O, aqueous EtOH or pet ether (b 60-80o). [Williams & Krynitsky Org Synth Coll Vol III 10 1955.]

105-45-3
62-53-3
102-01-2
Synthesis of Acetoacetanilide from Methyl acetoacetate and Aniline
Acetoacetanilide;Acetoacetic amilide;Acetoacetylaniline;α-Acetylacetanilide;β-Ketobutyranilide;3-Oxo-N-phenylbutanamide Acetoacetic amilide Butanamide, 3-oxo-N-phenyl- à-acetylacetanilide ACETOACETANILIDE 98+% AcetoacetanilideForSynthesis Naringenin 7b-neohesperidoside Acetoacetanilide,99% Cetoactanilide Acetoacetanilide, 99% 5GR AAA, Acetoacetaniline Acetoacetanilide >=99.5% .alpha.-Acetylacetanilide [(Acetoacetyl)amino]benzene 1-(Phenylcarbamoyl)-2-propanone 2-acetyl-acetanilid 3-oxo-,amide,n-phenyl-butanoicaci 3-oxo-n-phenyl-butanamid a-Acetylactanilide Acetanilide, 2-acetyl- Acetoacetamidobenzene Acetoacetonilide Acetoacetylaniline Acetylacetanilide alpha-Acetylacetanilide alpha-Acetyl-N-phenylacetamide Anilid kyseliny acetoctove anilidkyselinyacetoctove beta-Ketobutyranilide -Keto-butyranilide N-Acetoacetanilide USAF ek-1239 usafek-1239 B-KETOBUTYRANILIDE 2-acetyl-acetanilide N-Acetoacetylaniline Acetoacetanilide (flakes) Linazol N-Phenlyacetoacetamide TIMTEC-BB SBB003774 n-(acetylacetyl)aniline N-Phenyl-3-oxobutanamide 1-ACETYLACETANILIDE 3-OXO-N-PHENYLBUTYRAMIDE ACETOACETIC ANILIDE ACETOACETIC ACID ANILIDE ACETOACETANILIDE ((acetoacetyl)amino)benzene 4-(Phenylamino)-2,4-butanedione 4H-1-Benzopyran-4-one, 7-[[2-O-(6-deoxy-a-L-mannopyranosyl)-b-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (2S)- 7-[(2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chroman-4-one Coupler 633 AAA, Acetoacetanilid Acetoacetanilide 102-01-2 102-01-2 Acetoacetanilide Acetoacetanilide > AAN Acetoacetanilid