4'-aminoacetophenone
ethanone, 1-(4-aminophenyl)-
 
Notes:
None found
  • BOC Sciences
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      Product(s):
      99-92-3 Clenbuterol Impurity D > 95%
      4-Aminoacetophenone is a novel utilization of aminophenone derivative in toxicology, for treating intoxications with cyanogenic toxic substances.
       
       
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    • Penta International Corporation
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      Product(s):
      01-24200 p-AMINOACETOPHENONE
       
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      Product(s):
      A0251 4'-Aminoacetophenone >98.0%(T)
       
Synonyms   Articles   Notes   Search
CAS Number: 99-92-3Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 202-801-2
FDA UNII: 1S58KH902I
Nikkaji Web: J3.228J
Beilstein Number: 0471493
MDL: MFCD00007896
XlogP3: 0.80 (est)
Molecular Weight: 135.16593000
Formula: C8 H9 N O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: herbicides / pesticides
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 106.00 to  107.00 °C. @ 760.00 mm Hg
Boiling Point: 294.00 to  295.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.002000 mmHg @ 25.00 °C. (est)
Flash Point: 270.00 °F. TCC ( 132.10 °C. ) (est)
logP (o/w): 0.830
Soluble in:
 alcohol
 water, 3350 mg/L @ 37 °C (exp)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
Clenbuterol Impurity D > 95%
Odor: characteristic
Use: 4-Aminoacetophenone is a novel utilization of aminophenone derivative in toxicology, for treating intoxications with cyanogenic toxic substances.
Carbosynth
For experimental / research use only.
4'-Aminoacetophenone
Penta International
p-AMINOACETOPHENONE
Santa Cruz Biotechnology
For experimental / research use only.
4'-Aminoacetophenone
Sigma-Aldrich: Aldrich
For experimental / research use only.
4'-Aminoacetophenone 99%
TCI AMERICA
For experimental / research use only.
4'-Aminoacetophenone >98.0%(T)
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50  381 mg/kg
General Pharmacology. Vol. 14, Pg. 465, 1983.

intraperitoneal-rat LD50  260 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 80, Pg. 31, 1944.

oral-mouse LD50  596 mg/kg
General Pharmacology. Vol. 14, Pg. 465, 1983.

intraperitoneal-mouse LD50  300 mg/kg
National Technical Information Service. Vol. AD277-689

oral-bird - wild LD50  133 mg/kg
Archives of Environmental Contamination and Toxicology. Vol. 12, Pg. 355, 1983.

oral-dog LD  > 70 mg/kg
BLOOD: METHEMOGLOBINEMIA-CARBOXYHEMOGLOBIN
Journal of Pharmacology and Experimental Therapeutics. Vol. 80, Pg. 31, 1944.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: herbicides / pesticides
Recommendation for 4'-aminoacetophenone usage levels up to:
 not for fragrance use.
 
Recommendation for 4'-aminoacetophenone flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 99-92-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 7468
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 1-(4-aminophenyl)ethanone
Chemidplus: 0000099923
RTECS: AM5500000 for cas# 99-92-3
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References:
 1-(4-aminophenyl)ethanone
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 99-92-3
Pubchem (cid): 7468
Pubchem (sid): 134972215
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEMBL: View
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2922.39.4500
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 found in nature
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Synonyms:
 acetophenone, 4'-amino-
4-acetyl aniline
1-acetyl-4-aminobenzene
4-acetylaniline
p-acetylaniline
4-amino acetophenone
1-(4-amino-phenyl)-ethanone
4-aminoacetophenone
p-aminoacetophenone
para-aminoacetophenone
1-(4-aminophenyl) ethanone
1-(4-aminophenyl)-ethanone
1-(4-aminophenyl)ethanone
 ethanone, 1-(4-aminophenyl)-
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Articles:
PubMed: Phenylazoindole dyes--part I: the syntheses, characterizations, crystal structures, quantum chemical calculations and antimicrobial properties.
PubMed: Synthesis and evaluation of changes induced by solvent and substituent in electronic absorption spectra of some azo disperse dyes.
PubMed: A study of anti-inflammatory and analgesic activity of new 2,4,6-trisubstituted pyrimidines.
PubMed: Synthesis and immunomodulatory activites of new 5-hydrazino-3-methyl-4-isothiazolecarboxylic acid ethyl esters.
PubMed: Hydrogen bonding in the bromide salts of 4-aminobenzoic acid and 4-aminoacetophenone.
PubMed: Spectroscopic and biological studies on newly synthesized nickel(II) complexes of semicarbazones and thiosemicarbazones.
PubMed: Spectroscopic evaluation of manganese(II) complexes derived from semicarbazones and thiosemicarbazones.
PubMed: Involvement of proton transfer in the reductive repair of DNA guanyl radicals by aniline derivatives.
PubMed: Schiff bases of gossypol: an NMR and DFT study.
PubMed: EPR, mass, IR, electronic, and magnetic studies on copper(II) complexes of semicarbazones and thiosemicarbazones.
PubMed: Determination of thiopurine methyltransferase phenotype in isolated human erythrocytes using a new simple nonradioactive HPLC method.
PubMed: Analgesic activity of thioureido derivatives of arylsemicarbazones.
PubMed: Synthesis of aryl semicarbazone of 4-aminoacetophenone and their anti-HIV activity.
PubMed: Formation of 4,4-dialkoxycyclohexa-2,5-dienone N-(thiol-S-yl)imine during reaction of 4-alkoxynitrosobenzenes with thiols in alcoholic solvents.
PubMed: Determination of mitomycin C in human aqueous humor and serum by high-performance liquid chromatography.
PubMed: Identification of aromatic moieties and mycosamine in antifungal heptaenes with high-performance liquid chromatography, high-performance liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry.
PubMed: Comparison of metabolism and activity of an aryldimethyltriazene and an aryldiethyltriazene.
PubMed: Spectrophotometric methods for the determination of o-dihydroxybenzene derivatives.
PubMed: Further application of the diazotizationcoupling spectrophotometric technique to the determination of aromatic amines with 8-amino-1 -hydroxynaphthalene-3,6-disulphonic acid and N-(1-naphthyl)-ethylenediamine as coupling agents.
PubMed: Metabolism of the anticancer agent 1-(4-acetylphenyl)-3,3-dimethyltriazene.
PubMed: Studies of the mode of action of antitumour triazenes and triazines--IV. The metabolism of 1-(4-acetylphenyl)-3,3-dimethyltriazene.
PubMed: [Role of p-aminobenzoic acid in levorin biosynthesis].
PubMed: [Determination of p-aminoacetophenone and changes in its levels in a levorin producer depending on culture conditions].
PubMed: Location and analysis of 2-deoxy sugars on chromatograms and pherograms by fluorescence.
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