추천 제품
Quality Level
분석
≥98% (TLC)
양식
powder
광학 활성
[α]20/D -15.0 to -14.0 °, c = 2.5% (w/v) in hydrochloric acid
기술
thin layer chromatography (TLC): suitable
색상
white to off-white
mp
235 °C
solubility
0.5 M HCl: 50 mg/mL, clear, colorless to faintly yellow
저장 온도
2-8°C
SMILES string
N[C@H]([C@@H](O)[C@H](O)[C@H](O)CO)C(O)=O
InChI
1S/C6H13NO6/c7-3(6(12)13)5(11)4(10)2(9)1-8/h2-5,8-11H,1,7H2,(H,12,13)/t2-,3-,4-,5-/m1/s1
InChI key
UFYKDFXCZBTLOO-TXICZTDVSA-N
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기타 정보
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
Bin Wu et al.
Biotechnology progress, 27(1), 32-37 (2011-02-12)
D-glucosaminic acid was produced efficiently from glucosamine by oxidative fermentation using a newly isolated strain, Pseudomonas putida GNA5. After optimization of the fermentation process, 51.5 g L(-1) D-glucosaminic acid was produced from an initial concentration of 60 g L(-1) D-glucosamine-HCl
R Iwamoto et al.
FEBS letters, 156(1), 33-36 (1983-05-30)
The proton NMR analysis of D-glucosaminate dehydratase reaction in D2O revealed the incorporation of a deuterium atom at C-3 carbon of the product, 2-keto-3-deoxy-D-gluconate. Based on the chemical shift of C-3 proton of the product and the coupling constant characteristic
Jiali Zhang et al.
Marine drugs, 8(7), 1962-1987 (2010-08-18)
Chitosan has received much attention as a functional biopolymer for diverse applications, especially in pharmaceutics and medicine. Our recent efforts focused on the chemical and biological modification of chitosan in order to increase its solubility in aqueous solutions and absorbability
Use of D-glucosaminic acid as an internal standard in single-column accelerated amino acid analysis of physiological fluids.
C Stacey-Schmidt et al.
Analytical biochemistry, 123(1), 74-77 (1982-06-01)
T Yamaguchi et al.
Biological & pharmaceutical bulletin, 19(10), 1261-1265 (1996-10-01)
The DNA strand-breaking activity of some dihydropyrazine derivatives, 2,3-dihydro-5,6-dimethylpyrazine (3), 2,3-dihydro-2,5,6-trimethylpyrazine (4), 2,3-dihydro-2,2,5,6-tetramethylpyrazine (5), trans-2,3-dimethyl-5,6,7,8,9, 10-hexahydroquinoxaline (6), its cis-compound (7) and the mixture of 6 and 7 (8) was tested by agarose gel electrophoresis using plasmid pBR322 ccc-DNA as a
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