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L-Alaninol

L-Alaninol structure

L-Alaninol 

structure
  • CAS No:

    2749-11-3

  • Formula:

    C3H9NO

  • Chemical Name:

    L-Alaninol

  • Synonyms:

    H-L-ALA-OL;H-ALANINOL;H-ALA-OL;H-ALA-OL S-(+)-2 AMINO-PROPANOL;L-(+)-ALANINOL;L-ALANINOL;L-ALANILOL;L-(+)-2-AMINO PROPANOL

  • Categories:

    Biochemical Engineering  >  Amino Acids and Derivatives

Description

Colorless liquid


(S)-2-aminopropan-1-ol is an amino alcohol that is L-alanine in which the carboxy group has been reduced to the corresponding alcohol. It is an amino alcohol, a primary alcohol and a primary amino compound. It is a conjugate base of a (S)-2-aminopropan-1-ol(1+).


Purify it as for S-2-amino-3-methylbutan-1-ol below. [Beilstein 4 IV 1615.]

L-Alaninol Basic Attributes

75.11

75.11

1718865

220-388-7

V403GH89L1

Clear colorless to yellow

29221990

Characteristics

46.25000

-1

clear to pale yellow liquid

0.965 g/mL at 25 °C(lit.)

-2°C

72-73 °C11 mm Hg(lit.)

62ºC

n20/D1.450

Completely miscible in water

2-8ºC

0.373mmHg at 25°C

12.88±0.10(Predicted)

Keep in dark place,Inert atmosphere,2-8°C

Safety Information

III

8

UN 2735

3

C,Xi

26-36/37/39-45-36

C

P280-P305 + P351 + P338-P310

34-36/37/38

UN 2735 8/PG 2

|Danger|H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501|Aggregated GHS information provided by 97 companies from 4 notifications to the ECHA C&L Inventory.

Drug Information

2-aminopropanol|(S)-2-amino-1-propanol

L-Alaninol Use and Manufacturing

S-(+)-2-Amino-1-propanol is an aliphatic amino alcohol shown to induce an antiproliferative effect in B16 melanoma cells. S-(+)-2-Amino-1-propanol is used in the preparation of oxazolines which are often used as ligands in homogeneous catalysis.


(S)-(+)-2-Amino-1-propanol (L-Alaninol) may be used in the preparation of unsymmetrical tridentate Schiff base ligands via condensation with carbonyl compounds. It may also be used as a chiral auxillary for the preparation oftert-butyl 4-N-[(2-hydroxy-1-(S)-methyl)ethylamino]-2-methylene-4-(S)-phenyl-butyrate.

Computed Properties

Molecular Weight:75.11
XLogP3:-1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:75.068413911
Monoisotopic Mass:75.068413911
Topological Polar Surface Area:46.2
Heavy Atom Count:5
Complexity:22.9
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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