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About This Item
經驗公式（希爾表示法）:
C6H13NO5
CAS號碼:
分子量：:
179.17
MDL號碼:
分類程式碼代碼:
12352201
PubChem物質ID:
NACRES:
NA.25
暫時無法取得訂價和供貨情況
推薦產品
化驗
≥98% (TLC)
品質等級
形狀
powder
光學活性
[α]/D 60.00 to 64.00°, c = 18.00-22.00 mg/mL in water
技術
thin layer chromatography (TLC): suitable
儲存溫度
2-8°C
SMILES 字串
NC1OC(CO)C(O)C(O)C1O
InChI
1S/C6H13NO5/c7-6-5(11)4(10)3(9)2(1-8)12-6/h2-6,8-11H,1,7H2
InChI 密鑰
WCWOEQFAYSXBRK-UHFFFAOYSA-N
應用
β-D-Galactosylamine, a galactose analogue, is used as a competitive inhibitor to help isolate, purify, identify, differentiate and characterize β-D-galactosidase(s) and galactose oxidase(s).
其他說明
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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R A DiCioccio et al.
Carbohydrate research, 127(1), 109-120 (1984-04-02)
A beta-D-galactosidase from bovine liver was purified to apparent homogeneity. The major purification step was affinity chromatography on a column of D-galactose attached to a Sepharose support activated with divinyl sulfone. Affinity media prepared by binding ligands to Sepharose activated
C F Mazitsos et al.
Journal of chromatography. A, 954(1-2), 137-150 (2002-06-13)
Two anthraquinone galactosyl-biomimetic dye-ligands comprising, as terminal biomimetic moiety, galactose analogues (1-amino-1-deoxy-beta-D-galactose and D(+)-galactosamine) were designed for the enzyme galactose oxidase (GAO), using molecular modelling, synthesized and characterized. The biomimetic ligands were immobilized on agarose beads and the affinity adsorbents
N Monji et al.
Research communications in chemical pathology and pharmacology, 26(1), 187-196 (1979-10-01)
We have developed a new method for separation of antibody bound and unbound enzyme conjugates. The technique as applied to the assay of choriomammotropin involves the use of beta-D-galactosylamine bound to agarose to separate the unbound choriomammotropin-beta-galactosidase conjugates for antibody
Bo-Yu Li et al.
Carbohydrate research, 345(12), 1708-1712 (2010-06-30)
The highly diastereoselective InCl(3)-catalyzed aza-Friedel-Crafts reaction of substituted indoles with aldimines generated from Kunz's amine was studied. The reaction afforded the desired product in good to high yields with up to >19:1 diastereoselective ratios. The O-pivaloylated beta-D-galactosyl moiety could not
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