177350
1,2,3,4-Tetrahydro-1-naphthylamine hydrochloride
98%
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About This Item
Empirical Formula (Hill Notation):
C10H13N · HCl
CAS Number:
Molecular Weight:
183.68
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Assay:
98%
Form:
solid
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
SMILES string
Cl.NC1CCCc2ccccc12
InChI key
DETWFIUAXSWCIK-UHFFFAOYSA-N
assay
98%
form
solid
mp
185-187 °C (lit.)
density
0.974 g/mL at 25 °C (lit.)
Application
1,2,3,4-Tetrahydro-1-naphthylamine hydrochloride was used in enantiomeric separation using β-cyclodextrin-bonded negatively charged polyacrylamide gel-filled capillaries.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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
Effects of isomers of apomorphines on dopamine receptors in striatal and limbic tissue of rat brain.
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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