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质量水平
方案
98%
表单
liquid
折射率
n20/D 1.505 (lit.)
沸点
165 °C/740 mmHg (lit.)
密度
0.935 g/mL at 25 °C (lit.)
SMILES字符串
Cc1ccc(C)[nH]1
InChI
1S/C6H9N/c1-5-3-4-6(2)7-5/h3-4,7H,1-2H3
InChI key
PAPNRQCYSFBWDI-UHFFFAOYSA-N
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警示用语：
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
129.2 °F - closed cup
闪点(°C)
54 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Yoshiteru Matsumoto et al.
Physical chemistry chemical physics : PCCP, 13(31), 13962-13971 (2011-06-16)
N-H···π hydrogen-bonded (H-bonded) structures were studied by applying vibrational spectroscopy to self-aggregate clusters of 2,5-dimethylpyrrole (DMPy) and its binary clusters with pyrrole (Py). The NH stretching vibrations of jet-cooled clusters were observed by IR cavity ringdown spectroscopy. A combination of
M Zhu et al.
Journal of chromatography, 628(1), 37-47 (1993-01-01)
A method employing high-performance liquid chromatography with thermospray mass spectrometry (TSP-MS) and photodiode-array detection was developed and applied to the analysis of autoxidation products of 2,5-dimethyl-N-alkylpyrroles in aqueous solution under air or 18O2. Numerous oxidation products were separated, characterized and
Hongyin Yin et al.
PloS one, 8(9), e76011-e76011 (2013-10-08)
The formation of pyrrole adducts might be responsible for peripheral nerve injury caused by n-hexane. The internal dose of pyrrole adducts would supply more information for the neurotoxicity of n-hexane. The current study was designed to investigate the tissue distributions
Xianjie Li et al.
PloS one, 13(12), e0209939-e0209939 (2019-01-01)
Pyrrole adducts are specific reaction products of 2,5-hexadione (2,5-HD) in vivo and are considered highly relevant to the pathogenesis of peripheral nerve impairments after exposure to n-hexane, though the exact mechanism remains unclear. In this study, 40 male Wistar rats
Joseph M Beames et al.
The Journal of chemical physics, 131(17), 174305-174305 (2009-11-10)
The photophysical properties of porphyrins have relevance for their use as light-activated drugs in cancer treatment and sensitizers in solid-state solar cells. However, the appearance of their UV-visible spectra is usually explained inadequately by qualitative molecular-orbital theories. We intend to
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