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化驗
99%
形狀
liquid
折射率
n20/D 1.366 (lit.)
bp
97 °C (lit.)
mp
−93 °C (lit.)
溶解度
water: soluble 11.9g/100g at 40 °C
water: soluble 29g/100g at 100 °C
DMF: miscible
alcohol: miscible
diethyl ether: miscible
密度
0.772 g/mL at 25 °C (lit.)
官能基
nitrile
SMILES 字串
CCC#N
InChI
1S/C3H5N/c1-2-3-4/h2H2,1H3
InChI 密鑰
FVSKHRXBFJPNKK-UHFFFAOYSA-N
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一般說明
丙腈是一种实验性十二指肠溃疡诱导剂,能够刺激大鼠胃酸分泌。
應用
丙腈被用于介孔石墨C3N4催化的各种腈的环三聚反应,生成三嗪衍生物。它被用于研究邻甲酚与丙腈的复合物形成的拉曼光谱。
應用
产品编号
说明
价格
訊號詞
Danger
危險分類
Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 2
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 1
閃點(°F)
42.8 °F - closed cup
閃點(°C)
6 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Pathogenesis of duodenal ulcer. Gastric hyperacidity caused by propionitrile and cysteamine in rats.
S Szabo et al.
Research communications in chemical pathology and pharmacology, 16(2), 311-323 (1977-02-01)
Cysteamine and propionitrile, experimental duodenal ulcerogens, stimulated gastric acid secretion in the rat. Gastric acid secretion was measured by two separate methods, the conventional pylorus ligation technique and a non-invasive technique based on the pH dependent liberation of azure A
A Raman spectroscopic study of complex formation between o-cresol and propionitrile.
Girling RB and Shurvell HF.
Vibrational Spectroscopy, 18(1), 77-82 (1998)
Mesoporous graphitic carbon nitride as a versatile, metal-free catalyst for the cyclisation of functional nitriles and alkynes.
Goettmann F, et al.
New. J. Chem., 31(8), 1455-1460 (2007)
Oliver Kaumanns et al.
The Journal of organic chemistry, 74(1), 75-81 (2008-11-27)
The rates of the reactions of the colored para-substituted phenylacetonitrile anions 1a-c and the phenylpropionitrile anions 2a-c with Michael acceptors (3a-u) were determined by UV-vis spectroscopy in DMSO at 20 degrees C. The reactions follow second-order kinetics, and the corresponding
Atsushi Kunishita et al.
Inorganic chemistry, 47(18), 8222-8232 (2008-08-14)
The copper(II) complexes 1(H) and 1(Ar(X)), supported by the N,N-di(2-pyridylmethyl)benzylamine tridentate ligand (L(H)) or its derivatives having m-substituted phenyl group at the 6-position of pyridine donor groups (L(Ar(X))), have been prepared, and their reactivity toward H2O2 has been examined in
Chromatograms
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