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About This Item
Linear Formula:
H2NCH2CH(OH)CH2OH
CAS Number:
Molecular Weight:
91.11
Beilstein:
1719122
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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
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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).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
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