Identification | More | [Name]
3-Methylbutanenitrile | [CAS]
625-28-5 | [Synonyms]
3-methylbutanenitrile ISOAMYL NITRILE ISOBUTYL CYANIDE Isopenmnenitrile ISOVALERONITRILE 2-Methylbutane secondary mononitrile 2-methylbutanesecondarymononitrile 3-methyl-butanenitril 3-methyl-butyronitril 3-Methylbutyronitrile 3-methyl-butyronitrile Butanenitrile,3-methyl- Butyronitrile, 2-methyl- Butyronitrile, 3-methyl- iso-C4H9CN Isopentane nitrile isopentanenitrile ISOVALERONITRILE 98+% | [EINECS(EC#)]
210-884-1 | [Molecular Formula]
C5H9N | [MDL Number]
MFCD00001944 | [Molecular Weight]
83.13 | [MOL File]
625-28-5.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R10:Flammable. R22:Harmful if swallowed. R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [RIDADR ]
UN 1992 3/PG 3
| [WGK Germany ]
3
| [RTECS ]
NY1750000
| [HazardClass ]
3.2 | [PackingGroup ]
III | [HS Code ]
29269095 |
Hazard Information | Back Directory | [Uses]
Isovaleronitrile was used in the synthesis of a new type of nitrilase, arylacetonitrilase by Alcaligenes faecalis JM3 cells. | [Definition]
ChEBI: Isovaleronitrile is an aliphatic nitrile that is 2-methylpropane substituted by a cyano group at position 1. It has a role as a plant metabolite. It is an aliphatic nitrile and a volatile organic compound. | [General Description]
Isovaleronitrile induced Rhodococcus ATCC 39484 produced a nitrilase. |
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