Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

A59506

Sigma-Aldrich

1-Aminoindan

98%

Synonym(s):

1-Indanamine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C9H11N
CAS Number:
34698-41-4
Molecular Weight:
133.19
Beilstein:
3196205
EC Number:
252-158-7
MDL number:
MFCD00003799
UNSPSC Code:
12352100
PubChem Substance ID:
24891038
NACRES:
NA.22

Quality Level

100

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

Related Categories

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

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000233356
MKCV4563
MKCV2962
MKCL8119
MKCM0666

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service