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A59506

Sigma-Aldrich

1-Aminoindan

98%

Sinónimos:

1-Indanamine

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About This Item

Fórmula empírica (notación de Hill):
C9H11N
Número de CAS:
34698-41-4
Peso molecular:
133.19
Beilstein/REAXYS Number:
3196205
EC Number:
252-158-7
MDL number:
MFCD00003799
UNSPSC Code:
12352100
PubChem Substance ID:
24891038
NACRES:
NA.22

assay

98%

form

liquid

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

Categorías relacionadas

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

201.2 °F - closed cup

flash_point_c

94 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Chen Zhang et al.
Journal of chromatography. A, 1217(30), 4965-4970 (2010-06-18)
Separation of chiral primary amino compounds was efficiently achieved under reversed-phase high performance liquid chromatography (RP-HPLC) conditions using a mixture of non-chiral crown ether (18-crown-6) and dimethyl-beta-cyclodextrin (DM-beta-CD) in the mobile phase. Under these conditions, the amino group of the
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
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
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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