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Merck
CN

285633

4-二甲氨基苄胺 二盐酸盐

95%

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关于此项目

线性分子式:
(CH3)2NC6H4CH2NH2 · 2HCl
化学文摘社编号:
分子量:
223.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
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Quality Level

assay

95%

mp

220-224 °C (dec.) (lit.)

solubility

H2O: soluble 50 mg/mL, clear, faintly yellow to yellow

functional group

amine

SMILES string

Cl.Cl.CN(C)c1ccc(CN)cc1

InChI

1S/C9H14N2.2ClH/c1-11(2)9-5-3-8(7-10)4-6-9;;/h3-6H,7,10H2,1-2H3;2*1H

InChI key

NRZQHDOWSPJUQW-UHFFFAOYSA-N



pictograms

Exclamation mark

signalword

Warning

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

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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D E Edmondson et al.
Biochemistry, 32(19), 5196-5202 (1993-05-18)
The oxidative deamination of p-(N,N-dimethylamino)benzylamine and N-methyl-p-(N,N-dimethylamino)benzylamine by bovine liver monoamine oxidase B has been investigated by absorption spectral, steady-state, and stopped-flow kinetic studies. An absorbing intermediate with a maximum at 390 nm is observed with either analogue in turnover
Anna Mura et al.
FEBS letters, 580(18), 4317-4324 (2006-07-18)
Copper removal from pig kidney amine oxidase containing Cu/topaquinone (TPQ) has been obtained using CN(-) in the presence of the poor substrate p-(dimethylamino)benzylamine. Upon removal of copper, the enzyme loses its activity while the TPQ cofactor remains in its oxidized
A S Kimes et al.
Biochemical pharmacology, 31(16), 2639-2642 (1982-08-15)
Nitrobenzoid, nitroheterocyclic and cyanobenzoid compounds inhibit type B monoamine oxidase. A partially purified enzyme preparation from rabbit liver mitochondria, oxidizing rho-dimethyl-aminobenzylamine as the substrate, was competitively inhibited by nitrobenzoid compounds with K1 values in the range of 0.28 muM for



全球贸易项目编号

货号GTIN
285633-1G04061825770802
285633-5G04061832099293