D183601
2,5-二甲基吡咯
98%
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关于此项目
经验公式（希尔记法）:
C6H9N
化学文摘社编号:
分子量:
95.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-913-8
MDL number:
Assay:
98%
Form:
liquid
产品名称
2,5-二甲基吡咯, 98%
InChI key
PAPNRQCYSFBWDI-UHFFFAOYSA-N
InChI
1S/C6H9N/c1-5-3-4-6(2)7-5/h3-4,7H,1-2H3
SMILES string
Cc1ccc(C)[nH]1
assay
98%
form
liquid
refractive index
n20/D 1.505 (lit.)
bp
165 °C/740 mmHg (lit.)
density
0.935 g/mL at 25 °C (lit.)
Quality Level
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signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - 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
129.2 °F - closed cup
flash_point_c
54 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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
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
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
Xianjie Li et al.
Neurotoxicology, 78, 11-20 (2020-02-12)
n-Hexane has been reported to induce serious peripheral neuropathy in workers. Pyrrole adducts are the unique reaction products of n-hexane in organisms and have been demonstrated to be critical to n-hexane neuropathy. Our previous studies have demonstrated that pyrrole adducts
Ireneusz Nowak et al.
Organic letters, 5(18), 3345-3348 (2003-08-29)
[reaction: see text] Protection of the amino group of adenine and guanine nucleosides was effected by heating the substrates in 2,5-hexanedione. The resulting 2,5-dimethylpyrrole adducts were stable toward bases but were hydrolyzed with TFA/H(2)O to regenerate the amino function.
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