质量水平
方案
98%
折射率
n20/D 1.549 (lit.)
沸点
78-81 °C/10 mmHg (lit.)
密度
1.141 g/mL at 20 °C (lit.)
储存温度
2-8°C
SMILES字符串
[H]C(=O)c1cccnc1
InChI
1S/C6H5NO/c8-5-6-2-1-3-7-4-6/h1-5H
InChI key
QJZUKDFHGGYHMC-UHFFFAOYSA-N
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Warning
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
95.0 °F - closed cup
闪点(°C)
35 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
C C Shone et al.
Biochemistry, 20(26), 7494-7501 (1981-12-22)
Coenzyme A linked aldehyde dehydrogenase from Escherichia coli strain B has been purified to a specific activity of 14 units/mg of protein, and initial rate and substrate analogue inhibition experiments have been performed. On the basis of these steady-state measurements
P Narender et al.
Bioorganic & medicinal chemistry, 14(13), 4600-4609 (2006-03-03)
Baylis-Hillman acetates were synthesized from substituted 2-chloronicotinaldehydes and were conveniently transformed into multisubstituted quinolines and cyclopenta[g]quinolines on reaction with nitroethane or ethyl cyanoacetate via a successive S(N)2'-S(N)Ar elimination strategy. Thus, synthesized quinolines were evaluated for antimicrobial activity and found having
Hugo Destaillats et al.
Environmental science & technology, 40(6), 1799-1805 (2006-03-31)
Assessment of secondhand tobacco smoke exposure using nicotine as a tracer or biomarker is affected by sorption of the alkaloid to indoor surfaces and by its long-term re-emission into the gas phase. However, surface chemical interactions of nicotine have not
Sujin P Jose et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 64(1), 205-209 (2006-03-18)
The Fourier transform Raman and infrared spectra of nicotinaldehyde were recorded and the observed frequencies were assigned to various modes of vibration in terms of fundamentals by assuming Cs point group symmetry. A normal coordinate analysis was also carried out
K S De Jongh et al.
The Biochemical journal, 242(1), 143-150 (1987-02-15)
The kinetic mechanism of the major sheep liver aldehyde reductase (ALR1) was studied with three aldehyde substrates: p-nitrobenzaldehyde, pyridine-3-aldehyde and D-glucuronate. In each case the enzyme mechanism was sequential and product-inhibition studies were consistent with an ordered Bi Bi mechanism
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