Skip to Content
Merck
CN

308528

Isovaleronitrile

98%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
(CH3)2CHCH2CN
CAS Number:
Molecular Weight:
83.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-884-1
MDL number:
Assay:
98%
Form:
liquid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Level

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.)

functional group

nitrile

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

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

82.4 °F - closed cup

flash_point_c

28 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



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
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.
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



Global Trade Item Number

SKUGTIN
308528-25G04061836826338
308528-5G04061826674765