473960

Sigma-Aldrich

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

98%

Linear Formula:
H2NCH2CH(OH)CH2OH
CAS Number:
Molecular Weight:
91.11
Beilstein/REAXYS Number:
1719122
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

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.)

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

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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).

Packaging

1 g in glass bottle

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Precautionary Statements

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

UN 3259PSN1 8 / PGII

WGK Germany

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

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.
Kodama S, et al.
Electrophoresis, 28(21), 3930-3933 (2007)

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