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线性分子式:
(CH3)3N(Br)C6H5
化学文摘社编号:
分子量:
216.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
240-202-8
MDL number:
Beilstein/REAXYS Number:
3917006
产品名称
苯基三甲基溴化铵, 98%
InChI key
GNMJFQWRASXXMS-UHFFFAOYSA-M
InChI
1S/C9H14N.BrH/c1-10(2,3)9-7-5-4-6-8-9;/h4-8H,1-3H3;1H/q+1;/p-1
SMILES string
[Br-].C[N+](C)(C)c1ccccc1
assay
98%
technique(s)
titration: suitable
mp
215 °C (dec.) (lit.)
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Journal of photochemistry and photobiology. B, Biology, 100(2), 100-111 (2010-06-19)
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A Ranz et al.
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Cobalamin-dependent methionine synthase (MetH) catalyzes the transfer of methyl groups between methyltetrahydrofolate (CH(3)-H(4)folate) and homocysteine, with the enzyme-bound cobalamin serving as an intermediary in the methyl transfers. An MetH fragment comprising residues 2-649 contains modules that bind and activate CH(3)-H(4)folate
R W Gullick et al.
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A method has been established for the determination of four pharmaceutically active compounds (ibuprofen, ketoprofen, naproxen and clofibric acid) in water samples using dynamic hollow fiber liquid-phase microextraction (HF/LPME) followed by gas chromatography (GC) injection port derivatization and GC-mass spectrometric
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