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Sigma-Aldrich

4-(Dimethylamino)benzylamine dihydrochloride

95%

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About This Item

Linear Formula:
(CH3)2NC6H4CH2NH2 · 2HCl
CAS Number:
34403-52-6
Molecular Weight:
223.14
MDL number:
MFCD00012862
UNSPSC Code:
12352100
PubChem Substance ID:
24857222
NACRES:
NA.22

Assay

95%

mp

220-224 °C (dec.) (lit.)

solubility

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

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

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
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
J Ishida et al.
Journal of chromatography. B, Biomedical sciences and applications, 738(2), 199-206 (2000-03-16)
A selective and sensitive high-performance liquid chromatographic method with chemiluminescence detection for the determination of 5-hydroxyindoles is described, based on the reaction of 5-hydroxyindoles with 4-dimethylaminobenzylamine. Serotonin, 5-hydroxyindole-3-acetic acid, 5-hydroxytryptophol, 5-hydroxyindole-3-acetamide and N-acetyl-5-hydroxytryptamine were used as model compounds to optimize
R Medda et al.
Biochemistry, 34(50), 16375-16381 (1995-12-19)
Intermediate states in the catalytic mechanism of lentil copper amine oxidase have been investigated by ESR and optical spectroscopy. Using highly purified apo- and holoenzyme in combination with a poor substrate and a range of inhibitors, under both aerobic and
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