推荐产品
化驗
98%
光學活性
[α]20/D −28±1°, c = 4 in 5 M HCl
雜質
<0.5 mol
折射率
n20/D 1.483 (lit.)
bp
117-119 °C/0.4 mmHg (lit.)
密度
1.175 g/mL at 25 °C (lit.)
SMILES 字串
NC[C@H](O)CO
InChI
1S/C3H9NO2/c4-1-3(6)2-5/h3,5-6H,1-2,4H2/t3-/m0/s1
InChI 密鑰
KQIGMPWTAHJUMN-VKHMYHEASA-N
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應用
(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).
訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
235.4 °F - closed cup
閃點(°C)
113 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
其他客户在看
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.
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.
Electrophoresis, 27(23), 4730-4734 (2006)
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