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N-Acetylbenzoquinoneimine_Molecular_structure_CAS_50700-49-7)
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N-Acetylbenzoquinoneimine

Catalog No. A7300 Name Sigma Aldrich
CAS Number 50700-49-7 Website http://www.sigmaaldrich.com
M. F. C8H7NO2 Telephone 1-800-521-8956
M. W. 149.14668 Fax
Purity Email
Storage Chembase ID: 91335

SYNONYMS

Title
N-乙酰苯醌亚胺
IUPAC name
N-(4-oxocyclohexa-2,5-dien-1-ylidene)acetamide
IUPAC Traditional name
N-acetyl-p-benzoquinone
Synonyms
N-乙酰基对苯醌亚胺
N-(4-Oxo-1-cyclohexa-2,5-dienylidene)acetamide
NAPQI
N-Acetyl-p-benzo-quinoneimine

DATABASE IDS

MDL Number MFCD00078909
CAS Number 50700-49-7
PubChem SID 24891199

PROPERTIES

Empirical Formula (Hill Notation) C8H7NO2
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
RTECS AC6960000
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Other Notes
Acetaminophen metabolite that reacts with serum proteins.
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. A7300.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Packaging
1, 5 mg in serum btl
Application
Reactant involved in:
• Redox reactions1
• Hydrohalogenation2
• pH dependent reactions: in acidic media it is hydrolyzed, hydroxylated in alkaline media, and dimerized at intermediate pHs3
• Mediation of acetaminophen hepatotoxicity4
• Studies to identify the utility of acetaminophen for treating autoimmune disorders5
Description (简体中文)
Other Notes
对乙酰氨基酚代谢物,可与血清蛋白发生反应。
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. A7300.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
包装
1, 5 mg in serum btl
Application
Reactant involved in:
• Redox reactions1
• Hydrohalogenation2
• pH dependent reactions: in acidic media it is hydrolyzed, hydroxylated in alkaline media, and dimerized at intermediate pHs3
• Mediation of acetaminophen hepatotoxicity4
• Studies to identify the utility of acetaminophen for treating autoimmune disorders5

REFERENCES