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A59506

Sigma-Aldrich

1-Aminoindan

98%

Synonym(e):

1-Indanamin

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About This Item

Empirische Formel (Hill-System):
C9H11N
CAS-Nummer:
34698-41-4
Molekulargewicht:
133.19
Beilstein:
3196205
EG-Nummer:
252-158-7
MDL-Nummer:
MFCD00003799
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24891038
NACRES:
NA.22

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.561 (lit.)

bp

96-97 °C/8 mmHg (lit.)

mp (Schmelzpunkt)

15 °C (lit.)

Dichte

1.038 g/mL at 25 °C (lit.)

Lagertemp.

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

InChIKey

XJEVHMGJSYVQBQ-UHFFFAOYSA-N

Verwandte Kategorien

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

201.2 °F - closed cup

Flammpunkt (°C)

94 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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Rasagiline mesylate ≥98% (HPLC)

Sigma-Aldrich

SML0124

Rasagiline mesylate

Ribonuklease A aus Rinderpankreas Type III-A, ≥85% RNase A basis (SDS-PAGE), 85-140 Kunitz units/mg protein

Sigma-Aldrich

R5125

Ribonuklease A aus Rinderpankreas

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
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
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
Tasuku Isozaki et al.
The Journal of chemical physics, 126(21), 214304-214304 (2007-06-15)
The UV-UV hole-burning spectra of the jet-cooled 1-aminoindan were measured for the first time. Complicated spectral features observed in the laser-induced fluorescence excitation spectrum due to two conformers, R and B, were firmly separated. On the basis of fluorescence measurements
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