A59506
1-Aminoindan
98%
Synonym(s):
1-Indanamine
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About This Item
Empirical Formula (Hill Notation):
C9H11N
CAS Number:
Molecular Weight:
133.19
Beilstein:
3196205
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
98%
form
liquid
drug control
Új pszichoaktív anyag / New psychoactive substance (Hungary), 78/2022. (XII. 28.) BM rendelet
refractive index
n20/D 1.561 (lit.)
bp
96-97 °C/8 mmHg (lit.)
mp
15 °C (lit.)
density
1.038 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
NC1CCc2ccccc12
InChI
1S/C9H11N/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9H,5-6,10H2
InChI key
XJEVHMGJSYVQBQ-UHFFFAOYSA-N
Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
201.2 °F - closed cup
Flash Point(C)
94 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Fumihiko Kitagawa et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 21(1), 61-65 (2005-01-29)
Chiral separations of 1-aminoindan (AI) by cyclodextrin electrokinetic chromatography (CDEKC) were investigated on microfluidic quartz chips. By using a microchip electrophoresis (MCE) instrument equipped with a linear-imaging UV detector, the separation process of the enantiomeric compounds was observed. When sulfated
L Zhou et al.
Journal of capillary electrophoresis, 4(6), 279-285 (1998-11-25)
Aminoindanol poses an interesting separation problem because it contains two chiral centers and exists as four stereoisomers. The capillary electrophoretic separation of the cis- and the larger trans-diastereomers of aminoindanol is simply achieved by pH control of the tris buffer
Wilfried Dimpfel et al.
Neuropsychobiology, 62(4), 213-220 (2010-08-18)
Rasagiline and selegiline are classified as monoamine oxidase B (MAO-B) inhibitors. The present investigation deals with time-dependent electrical frequency changes (electropharmacograms) induced by these, as well as by aminoindan, the major metabolite of rasagiline. Adult rats (day-night converted, >5 months
Sofia Glezer et al.
European journal of pharmacology, 472(3), 173-177 (2003-07-23)
The selective monoamine oxidase-B inhibitor selegiline (deprenyl) causes sympathomimetic effects and is metabolised to R(-)-methamphetamine and R(-)-amphetamine. The new monoamine oxidase-B inhibitor rasagiline is devoid of sympathomimetic effects and is metabolised to R(+)-1-aminoindan. Sympathomimetic effects of methamphetamine and 1-aminoindan enantiomers
James M Graham et al.
Bioorganic & medicinal chemistry letters, 18(2), 489-493 (2007-12-28)
As part of an on-going effort to investigate the chemical space requirements for D(2)/5-HT(2A) receptor antagonists as atypical antipsychotics, new 1-aminoindanes were synthesized. The replacement of the heterocycle (oxindole) in ziprasidone with a carbocycle (indane) was well tolerated and was
Chromatograms
suitable for GC
application for HPLC
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