76671
丙腈
analytical standard
别名:
乙基氰
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关于此项目
线性分子式:
CH3CH2CN
化学文摘社编号:
分子量:
55.08
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
203-464-4
Beilstein/REAXYS Number:
773680
MDL number:
InChI key
FVSKHRXBFJPNKK-UHFFFAOYSA-N
InChI
1S/C3H5N/c1-2-3-4/h2H2,1H3
SMILES string
CCC#N
grade
analytical standard
assay
≥99.5% (GC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
Quality Level
bp
97 °C (lit.)
mp
−93 °C (lit.)
density
0.772 g/mL at 25 °C (lit.)
application(s)
environmental
format
neat
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Application
Propionitrile may be used as a mobile phase for the separation and elution of triglycerides in cocoa butter samples using reversed-phase high-performance liquid chromatography with refractive index detector and temperature programming.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
signalword
Danger
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
42.8 °F - closed cup
flash_point_c
6 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
监管及禁止进口产品
此项目有
Improved HPLC of triglycerides by special tempering procedures
Frede E
Chromatographia, 21(1), 29-36 (1986)
M Cantarella et al.
Journal of industrial microbiology & biotechnology, 33(3), 208-214 (2005-03-02)
The biohydration of acrylonitrile, propionitrile and benzonitrile catalysed by the NHase activity contained in resting cells of Microbacterium imperiale CBS 498-74 was operated at 5, 10 and 20 degrees C in laboratory-scale batch and membrane bioreactors. The bioreactions were conducted
D Somjen et al.
Journal of cellular biochemistry, 112(2), 625-632 (2011-01-27)
In cultured human osteoblasts estradiol-17β (E2) modulated DNA synthesis, the specific activity of creatine kinase BB (CK), 12 and 15 lipoxygenase (LO) mRNA expression and formation of 12- and 15-hydroxyeicosatetraenoic acid (HETE). We now investigate the response of human bone
Hayley J Andreazza et al.
Organic & biomolecular chemistry, 4(12), 2466-2472 (2006-06-10)
Franck-Condon one-electron oxidation of the stable anions -CH2CN, CH3-CHCN and -CH2CH2CN (in the collision cell of a reverse-sector mass spectrometer) produce the radicals .CH2CN, CH3.CHCN and .CH2CH2CN, which neither rearrange nor decompose during the microsecond duration of the neutralisation-reionisation experiment.
H V O Carswell et al.
American journal of physiology. Heart and circulatory physiology, 287(4), H1501-H1504 (2004-05-25)
The present study employs selective estrogen receptor (ER) agonists to determine whether 17beta-estradiol-induced neuroprotection in global ischemia is receptor mediated and, if so, which subtype of receptor (ERalpha or ERbeta) is predominantly responsible. Halothane-anesthetized female C57Bl/6J mice were ovariectomized, and
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