DL-ALANINOL HYDROCHLORIDE

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Names

[ CAS No. ]:
17016-92-1

[ Name ]:
DL-ALANINOL HYDROCHLORIDE

[Synonym ]:
DL-Alaninol hydrochloride
DL-ALANINOL HCL
2-aminopropanol hydrochloride
2-Aminopropan-1-ol hydrochloride
1-Propanol,2-amino-,hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
174.5ºC at 760mmHg

[ Molecular Formula ]:
C3H10ClNO

[ Molecular Weight ]:
111.57100

[ Flash Point ]:
83.9ºC

[ Exact Mass ]:
111.04500

[ PSA ]:
46.25000

[ LogP ]:
0.82820

[ Vapour Pressure ]:
0.0766mmHg at 25°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

Articles

Conformational effects in photoelectron circular dichroism of alaninol.

ChemPhysChem 10 , 1839-1846, (2009)

A photoelectron circular dichroism (CD) study of the valence states of 2-amino-1-propanol (alaninol) in the gas phase is presented. The aim of the investigation is to reveal conformer population effec...

Chirality transfer from a single chiral molecule to 2D superstructures in alaninol on the Cu(100) surface.

Langmuir 27 , 7410-7418, (2011)

The formation of 2D chiral monolayers obtained by self-assembly of chiral molecules on surfaces has been widely reported in the literature. Control of chirality transfer from a single molecule to surf...

Probing enantioselectivity on chirally modified Cu(110), Cu(100), and Cu(111) surfaces.

Langmuir 26 , 16412-16423, (2010)

Temperature programmed desorption methods have been used to probe the enantioselectivity of achiral Cu(100), Cu(110), and Cu(111) single crystal surfaces modified by chiral organic molecules including...


More Articles

Related Compounds

  • DL-Alaninol
  • DL-3-(2-CHLOROPHENYL)-BETA-ALANINOL HCL
  • N-tert-Butyloxycarbonyl DL-Alaninol Methyl Ether
  • (S)-beta-(4-bromophenyl)alaninol hydrochloride
  • 2-(methylamino)propan-1-ol
  • Benzamide, N-(2-hydroxy-1-methylethyl)-
  • N1-(3-(2-chlorophenyl)-5-methyl-2-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-7-yl)-N2,N2-diethylethane-1,2-diamine
  • 1-[3-(2-chlorophenyl)-5-methyl-2-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-7-yl]-3,5-dimethyl-1H-pyrazole
  • ethyl 5-amino-1-[3-(2-chlorophenyl)-5-methyl-2-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-7-yl]-1H-pyrazole-4-carboxylate
  • 4-Chloro-2-isobutylpyridine
  • 3-(2-chlorophenyl)-5-methyl-N-(2-morpholinoethyl)-2-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-7-amine
  • 3-(2-Chlorophenyl)-5-methyl-7-(pyrrolidin-1-yl)-2-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine
  • 3-(2-chlorophenyl)-5-methyl-N-(pyridin-3-ylmethyl)-2-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-7-amine
  • 3-(2-chlorophenyl)-5-methyl-N-(pyridin-2-ylmethyl)-2-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-7-amine
  • 3-(2-chlorophenyl)-5-methyl-N-((tetrahydrofuran-2-yl)methyl)-2-(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-7-amine
  • 4-butoxy-N-(3-methylisoxazol-5-yl)benzamide
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