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177350

Sigma-Aldrich

1,2,3,4-Tetrahydro-1-naphthylamine hydrochloride

98%

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Empirical Formula (Hill Notation):
C10H13N · HCl
CAS Number:
49800-23-9
Molecular Weight:
183.68
MDL number:
MFCD00051984
UNSPSC Code:
12352100
PubChem Substance ID:
24850630

Assay

98%

form

solid

mp

185-187 °C (lit.)

density

0.974 g/mL at 25 °C (lit.)

SMILES string

Cl.NC1CCCc2ccccc12

InChI

1S/C10H13N.ClH/c11-10-7-3-5-8-4-1-2-6-9(8)10;/h1-2,4,6,10H,3,5,7,11H2;1H

InChI key

DETWFIUAXSWCIK-UHFFFAOYSA-N

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Application

1,2,3,4-Tetrahydro-1-naphthylamine hydrochloride was used in enantiomeric separation using β-cyclodextrin-bonded negatively charged polyacrylamide gel-filled capillaries.

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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T Koide et al.
Journal of chromatography. A, 893(1), 177-187 (2000-10-24)
Enantiomeric separation by capillary electrochromatography with beta-cyclodextrin-bonded negatively charged polyacrylamide gels was examined. The columns used are capillaries filled with a negatively charged polyacrylamide gel, a so-called monolithic stationary phase, to which allyl carbamoylated beta-CD (AC-beta-CD) derivatives covalently bind. The
J S Shin et al.
Biotechnology and bioengineering, 73(3), 179-187 (2001-03-21)
A kinetic resolution process for the production of chiral amines was developed using an enzyme-membrane reactor (EMR) and a hollow-fiber membrane contactor with (S)-specific omega-transaminases (omega-TA) from Vibrio fluvialis JS17 and Bacillus thuringiensis JS64. The substrate solution containing racemic amine
N S Kula et al.
Life sciences, 37(11), 1051-1057 (1985-09-16)
The optical isomers of apomorphine (APO) and N-propylnorapomorphine (NPA) were interacted with three biochemical indices of dopamine (DA) receptors in extrapyramidal and limbic preparations of rat brain tissue. There were consistent isomeric preferences for the R(-) configuration of both DA
Oxygen-18 studies on the oxidative deamination mechanism of alicyclic primary amines in rabbit liver microsomes.
H Kurebayashi et al.
Archives of biochemistry and biophysics, 215(2), 433-443 (1982-05-01)

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