N-N-BUTYL-N-BUTAN-4-OL-NITROSAMINE
N-N-BUTYL-N-BUTAN-4-OL-NITROSAMINE Basic information
- Product Name:
- N-N-BUTYL-N-BUTAN-4-OL-NITROSAMINE
- Synonyms:
-
- N-BUTYL-N-(4-HYDROXYBUTYL)NITROSAMIN
- N-N-BUTYL-N-BUTAN-4-OL-NITROSAMINE
- N-BUTYL-N-(4-HYDROXYBUTYL)NITROSAMINE
- N-BUTYL-N-NITROSO-4-AMINOBUTANOL
- N-BUTYL-N-BUTAN-4-OL-NITROSAMINE
- N-BUTYL-N-BUTANOLNITROSAMINE
- 1-Butanol, 4-(butylnitrosamino)-
- 4-(1-Butyl-2-oxohydrazino)-1-butanol
- CAS:
- 3817-11-6
- MF:
- C8H18N2O2
- MW:
- 174.24
- EINECS:
- 625-015-5
- Mol File:
- 3817-11-6.mol
N-N-BUTYL-N-BUTAN-4-OL-NITROSAMINE Chemical Properties
- Boiling point:
- 167 °C / 5mmHg
- Density
- 1.01
- refractive index
- 1.4700-1.4740
- Flash point:
- 147 °C
- storage temp.
- 2-8°C
- form
- clear liquid
- pka
- 15.03±0.10(Predicted)
- color
- Light yellow to Amber to Dark green
- Stability:
- Stability
- EPA Substance Registry System
- 4-(Butylnitrosoamino)butanol (3817-11-6)
N-N-BUTYL-N-BUTAN-4-OL-NITROSAMINE Usage And Synthesis
Chemical Properties
red liquid
Uses
N-Butyl-N-(4-hydroxybutyl)nitrosamine (BBN), a carcinogen, is used to induce histiologically relevant aggressive urinary bladder cancer in animal models.
Definition
ChEBI: A nitrosamine that has butyl and 4-hydroxybutyl substituents. In mice, it causes high-grade, invasive cancers in the urinary bladder, but not in any other tissues.
General Description
Dark red liquid.
Air & Water Reactions
Water soluble.
Reactivity Profile
A hydroxylated and nitrated amine. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.
Biochem/physiol Actions
Carcinogen used to induce urinary bladder cancer in animal models. The result of exposure is histologically comparable to human urinary bladder tumorigenesis. Used in chemopreventative studies.
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