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473960

(S)-3-Amino-1,2-propanediol

Name: (<I>S</I>)-3-Amino-1,2-propanediol
Brand: ALDRICH

98%

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About This Item

Linear Formula:

H₂NCH₂CH(OH)CH₂OH

CAS Number:

61278-21-5

Molecular Weight:

91.11

UNSPSC Code:

12352116

NACRES:

NA.22

PubChem Substance ID:

24870946

MDL number:

MFCD00798260

Beilstein/REAXYS Number:

1719122

Assay:

98%

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Properties

assay

98%

optical activity

[α]20/D −28±1°, c = 4 in 5 M HCl

impurities

<0.5 mol

refractive index

n20/D 1.483 (lit.)

bp

117-119 °C/0.4 mmHg (lit.)

density

1.175 g/mL at 25 °C (lit.)

functional group

amine, hydroxyl

SMILES string

NC[C@H](O)CO

InChI

1S/C3H9NO2/c4-1-3(6)2-5/h3,5-6H,1-2,4H2/t3-/m0/s1

InChI key

KQIGMPWTAHJUMN-VKHMYHEASA-N

Description

Application

(S)-3-Amino-1,2-propanediol-borate system can be used for the enantioseparation of monosaccharides, derivatized with either 1-phenyl-3-methyl-5-pyrazolone (PMP) or 8-aminonaphthalene-1,3,6-trisulfonate (ANT) by chiral ligand-exchange capillary electrophoresis (CE).

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Chiral resolution of monosaccharides as 1-phenyl-3-methyl-5-pyrazolone derivatives by ligand-exchange CE using borate anion as a central ion of the chiral selector.

Kodama S, et al.

Electrophoresis, 27(23), 4730-4734 (2006)

Simultaneous chiral resolution of monosaccharides as 8-aminonaphthalene-1, 3, 6-trisulfonate derivatives by ligand-exchange CE using borate as a central ion of the chiral selector.