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308528

Sigma-Aldrich

Isovaleronitrile

98%

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About This Item

Linear Formula:
(CH3)2CHCH2CN
CAS Number:
625-28-5
Molecular Weight:
83.13
EC Number:
210-884-1
MDL number:
MFCD00001944
UNSPSC Code:
12352100
PubChem Substance ID:
24858675
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.393 (lit.)

bp

128-130 °C/730 mmHg (lit.)

density

0.795 g/mL at 25 °C (lit.)

SMILES string

CC(C)CC#N

InChI

1S/C5H9N/c1-5(2)3-4-6/h5H,3H2,1-2H3

InChI key

QHDRKFYEGYYIIK-UHFFFAOYSA-N

General description

Isovaleronitrile induced Rhodococcus ATCC 39484 produced a nitrilase.

Application

Isovaleronitrile was used in the synthesis of a new type of nitrilase, arylacetonitrilase by Alcaligenes faecalis JM3 cells.

Pictograms

FlameSkull and crossbones
GHS02,GHS06

Signal Word

Danger

Hazard Statements

H226,H301,H315,H319,H335

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

82.4 °F - closed cup

Flash Point(C)

28 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sigma-Aldrich

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D E Stevenson et al.
Biotechnology and applied biochemistry, 15(3), 283-302 (1992-06-01)
Rhodococcus ATCC 39484 produced a nitrilase when induced with isovaleronitrile. The enzyme was obtainable pure in milligram amounts, had a subunit Mr of 40 kDa, and demonstrated a substrate-induced activation related to aggregation of subunits to form a 560-kDa complex.
Luyang Cai et al.
Water research, 177, 115803-115803 (2020-04-18)
Previous studies have focused on investigating the formation of odorous by-products during the chlorination of free amino acids (AAs). However, studies on the formation of odorous by-products during the chlorination of combined AAs, which are much more abundant in natural
Ji-Dong Shen et al.
Critical reviews in biotechnology, 41(1), 72-93 (2020-10-14)
Nitrilases are widely distributed in nature and are able to hydrolyze nitriles into their corresponding carboxylic acids and ammonia. In industry, nitrilases have been used as green biocatalysts for the production of high value-added products. To date, biocatalysts are considered
T Nagasawa et al.
European journal of biochemistry, 194(3), 765-772 (1990-12-27)
A new type of nitrilase, arylacetonitrilase, has been purified from isovaleronitrile-induced cells of Alcaligenes faecalis JM3 in four steps. The purity of the enzyme was confirmed by SDS/polyacrylamide gel electrophoresis, ampholyte electrofocusing and double immunodiffusion in agarose. The enzyme has

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