D-Glucosamine 6-phosphate

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Names

[ CAS No. ]:
3616-42-0

[ Name ]:
D-Glucosamine 6-phosphate

[Synonym ]:
D-glucosamine-6-phosphate
D-Glucosamine 6-Phosphate Hydrate
2-Amino-2-deoxy-D-glucose 6-phosphoric acid
O6-Phosphono-D-glucosamin
2-amino-2-deoxy-D-glucose-6-phosphate
(5-amino-2,3,4-trihydroxy-6-oxo-hexoxy)phosphonic acid
GlcN-6-P
2-Amino-O6-phosphono-2-desoxy-D-glucose
D-glucosamine 6-phosphate free acid
2-amino-O6-phosphono-2-deoxy-D-glucose
2-AMino-2-deoxy-D-glucose 6-(Dihydrogen Phosphate)
GLUCOSAMINE-6-PHOSPHATE
D-GLUCOSAMINE 6-PHOSPHATE

Chemical & Physical Properties

[ Density]:
1.817g/cm3

[ Boiling Point ]:
599.3ºC at 760mmHg

[ Molecular Formula ]:
C6H14NO8P

[ Molecular Weight ]:
259.15

[ Flash Point ]:
316.2ºC

[ Exact Mass ]:
259.04600

[ PSA ]:
172.51000

[ Index of Refraction ]:
1.585

[ Storage condition ]:
-20°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2922509090

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Studies on the Formation of Maillard and Caramelization Products from Glucosamine Incubated at 37 °C.

J. Agric. Food Chem. 63 , 6249-61, (2015)

This experiment compared the in vitro degradation of glucosamine (GlcN), N-acetylglucosamine, and glucose in the presence of NH3 incubated at 37 °C in phosphate buffer from 0.5 to 12 days. The reactio...

Design and synthesis of novel cell wall inhibitors of Mycobacterium tuberculosis GlmM and GlmU.

Carbohydr. Res. 346(13) , 1714-20, (2011)

GlmM and GlmU are key enzymes in the biosynthesis of UDP-N-acetyl-d-glucosamine (UDP-GlcNAc), an essential precursor of peptidoglycan and the rhamnose-GlcNAc linker region in the mycobacterial cell wa...

Evidence that adrenal hexose-6-phosphate dehydrogenase can effect microsomal P450 cytochrome steroidogenic enzymes.

Biochim. Biophys. Acta 1833(9) , 2039-44, (2013)

The role of adrenal hexose-6-phosphate dehydrogenase in providing reducing equivalents to P450 cytochrome steroidogenic enzymes in the endoplasmic reticulum is uncertain. Hexose-6-phosphate dehydrogen...


More Articles


Related Compounds

  • Borate(1-), trifluoro-3-pyridinyl-, (T-4)-
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  • Diethyl 2-nitrosomalonate
  • 2-(2-bromo-4-chlorophenoxy)Benzenamine
  • Ethyl 1-butylindole-2-carboxylate
  • methyl 2-((1-(4-fluorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)thio)propanoate
  • 4-amino-3-nitro-1-phenyl-1,8-naphthyridin-2(1H)-one
  • (2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S,19S)-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol
  • 4,4-Dimethyl-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid
  • 1-(4-Chlorophenyl)-3-hydroxy-3-(thiophen-2-yl)-2,3,5,6,7,8-hexahydroimidazo[1,2-a]pyridin-1-ium bromide
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