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285633

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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
Ricardo Cerón-Camacho et al.
Inorganic chemistry, 47(11), 4988-4995 (2008-05-08)
Mild electrophilic C(sp2)-H cyclometalation of 2-phenylpyridine and N,N-dimethylbenzylamine by the chloro-bridged osmium(II) dimer [OsCl(micro-Cl)(eta6-C6H6)]2 in acetonitrile affords cyclometalated pseudotetrahedral OsII complexes [Os(C approximately N)(eta6-C6H6)(NCMe)]PF6 (C approximately N=o-C6H4py-kappa C,N (2) and o-C6H4CH2NMe2-kappa C,N (5), respectively) in good to excellent yields. The
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