Substance

ID:350177

Names and Identifiers
IUPAC name
3-({[(methoxycarbonyl)amino]imino}methyl)quinoxaline-1,4-diium-1,4-bis(olate)
IUPAC Traditional name
3-({[(methoxycarbonyl)amino]imino}methyl)quinoxaline-1,4-diium-1,4-bis(olate)
Synonyms
Carbadox3-(2-Quinoxalinylmethylene)carbazic acid methyl ester N,N′-dioxide
Registration numbers
EC Number
CAS Number
PubChem SID
MDL Number
Properties
Safety Information
GHS Hazard statements
H228-H302-H350
UN Number
1325
RID/ADR
UN 1325 4.1/PG 2
GHS Pictograms
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS08
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
GHS02
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
GHS Signal Word
Danger
MSDS Link
Storage Temperature
2-8°C
European Hazard Symbols
Flammable Flammable (F)
Toxic Toxic (T)
Safety Statements
53-45
Risk Statements
45-11-22
Hazard Class
4.1
Packing Group
2
German water hazard class
3
GHS Precautionary statements
P201-P210-P308+P313
Product Information
Suitability
suitable for 1694 per US EPA
Empirical Formula (Hill Notation)
C11H10N4O4
Physical Property
Flash Point
18 °C
64.4 °F
Molecule Details
Application
Carbadox has been used to suppress aldosterone production, to study the spread of shiga toxin-producing Escherichia coli (STEC) strains 1, and to compare different antimicrobial activities 2.
Carbadox is used to suppress aldosterone production.
Molecular Spectra
No Data Available
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References
No Data Available
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