285633
4-(Dimethylamino)benzylamine dihydrochloride
95%
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Fórmula lineal:
(CH3)2NC6H4CH2NH2 · 2HCl
Número CAS:
Peso molecular:
223.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
Servicio técnico
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Permítanos ayudarleQuality 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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Clase de almacenamiento
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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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