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Merck
CN

366471

环戊腈

98%

别名:

氰基环戊烷, 环戊烷甲腈

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线性分子式:
C5H9CN
化学文摘社编号:
分子量:
95.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-229-2
Beilstein/REAXYS Number:
1098717
MDL number:
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产品名称

环戊腈, 98%

InChI key

SVPZJHKVRMRREG-UHFFFAOYSA-N

InChI

1S/C6H9N/c7-5-6-3-1-2-4-6/h6H,1-4H2

SMILES string

N#CC1CCCC1

assay

98%

form

liquid

refractive index

n20/D 1.441 (lit.)

bp

67-68 °C/10 mmHg (lit.)

mp

−76 °C (lit.)

density

0.912 g/mL at 25 °C (lit.)

functional group

nitrile

Quality Level

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Application

Cyclopentanecarbonitrile is suitable for use as substrate to investigate the specific activity of nitrile- and amide- hydrolyzing enzymes isolated from Candida guilliermondii UFMG-Y65 cells. It is suitable for use as reagent to investigate the nitrile degradation by Candida guilliermondii CCT 7207 using free and immobilized cell systems.

General description

Cyclopentanecarbonitrile is an alicyclic nitrile.

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

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

132.8 °F - closed cup

flash_point_c

56 °C - closed cup

ppe

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

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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J C Dias et al.
Canadian journal of microbiology, 46(6), 525-531 (2000-07-29)
Candida guilliermondii UFMG-Y65, isolated from a gold mine, was able to utilize different nitriles and the corresponding amides as sole source of nitrogen, at concentrations up to 2 M. Resting cells cultivated on YCB-acetonitrile medium showed nitrile hydrolyzing enzyme activities
J C Dias et al.
Applied microbiology and biotechnology, 56(5-6), 757-761 (2001-10-17)
Nitrile degradation by Candida guilliermondii CCT 7207 using free and immobilized cell systems was compared. Different specific growth rates were observed for immobilized (mumax=0.021 h(-1)) and the free cells (mumax=0.029 h(-1)). The maximum specific rate of acetic acid formation was

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