Basic information Safety Supplier Related

(S)-(+)-1-Aminoindan

Basic information Safety Supplier Related

(S)-(+)-1-Aminoindan Basic information

Product Name:
(S)-(+)-1-Aminoindan
Synonyms:
  • (S)-(+)-1-Aminoindan,ChiPros?99+%,ee99+%
  • (S)-(+)-1-Aminoindane, ChiPros 99+%, ee 99+%
  • (1S)-1-Aminoindan
  • (1S)-1-Indanamine
  • (S)-Indan-1-amine
  • [(S)-1-Indanyl]amine
  • (S)-2,3-dihydro-1H-inden-1-amine hydrochloride
  • (S)-(+)-1-AMINOINDAN: CHIPROS 99%, EE 99%
CAS:
61341-86-4
MF:
C9H11N
MW:
133.19
Product Categories:
  • Intermediates & Fine Chemicals
  • Metabolites & Impurities
  • Chiral
  • Amines
  • Aromatics
  • Pharmaceuticals
  • Chiral Reagents
Mol File:
61341-86-4.mol
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(S)-(+)-1-Aminoindan Chemical Properties

Melting point:
15 °C
alpha 
20 º (c=1.5, CH3OH)
Boiling point:
96-97 °C8 mm Hg(lit.)
Density 
1.038 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.562(lit.)
Flash point:
202 °F
storage temp. 
Keep in dark place,Sealed in dry,2-8°C
solubility 
soluble in DMSO, Methanol
form 
Liquid
pka
9.44±0.20(Predicted)
color 
Clear yellow
optical activity
[α]20/D +16.5°, c = 1.5 in methanol
Water Solubility 
insoluble
Sensitive 
Air Sensitive
BRN 
2206708
Stability:
Hygroscopic
InChI
1S/C9H11N/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9H,5-6,10H2/t9-/m0/s1
InChIKey
XJEVHMGJSYVQBQ-VIFPVBQESA-N
SMILES
N[C@H]1CCc2ccccc12
CAS DataBase Reference
61341-86-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-52/53
Safety Statements 
26-36-37/39-61
RIDADR 
UN 3082 9 / PGIII
WGK Germany 
3
10-34
HS Code 
29214990
Storage Class
10 - Combustible liquids
Hazard Classifications
Aquatic Chronic 3
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

MSDS

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(S)-(+)-1-Aminoindan Usage And Synthesis

Chemical Properties

clear yellow liquid

Uses

(S)-1-Aminoindane is the S-enantiomer of 1-Aminoindane; the metabolite of the monoamine oxidase-B inhibitor Rasagiline (R126000).

Synthesis

Add 1.00 g (4.80 mmol) of di-(S-(+)-1-aminoindan)- D-tartrate to a 250 mL flask, 40 mL of water, heated with stirring to dissolve completely, cooled to room temperature, added 20% NaOH solution dropwise, adjusted the PH to 10, and extracted with 40 mL each time. Trichloromethane was extracted three times, the organic phases were combined, dried with anhydrous magnesium sulfate for 20 min, filtered and concentrated to obtain 0.97 g of light yellow liquid (S)-(+) . -1-aminoindan, ee value (HPLC method) was 79.6%, the yield was 97.0%.

(S)-(+)-1-AminoindanSupplier

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