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G9753

Sigma-Aldrich

α-D-Glucosamine 1-phosphate

Synonym(s):

2-Amino-2-deoxy-α-D-glucopyranosyl phosphate

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5 MG
€295.00
25 MG
€928.00
100 MG
€2,970.00

€295.00

Available to ship on04 April 2025Details

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5 MG
€295.00
25 MG
€928.00
100 MG
€2,970.00

About This Item

Empirical Formula (Hill Notation):
C6H14NO8P
CAS Number:
2152-75-2
Molecular Weight:
259.15
MDL number:
MFCD00070181
UNSPSC Code:
12352201
PubChem Substance ID:
24895380
NACRES:
NA.25

€295.00

Available to ship on04 April 2025Details

Request a Bulk Order

biological source

natural (inorganic)

Quality Level

300

Assay

≥97% (TLC)

form

powder

impurities

<8.5% water (Karl Fischer)

color

white

solubility

water: 100 mg/mL, clear, colorless

storage temp.

−20°C

SMILES string

NC1C(O)C(O)C(CO)OC1OP(O)(O)=O

InChI

1S/C6H14NO8P/c7-3-5(10)4(9)2(1-8)14-6(3)15-16(11,12)13/h2-6,8-10H,1,7H2,(H2,11,12,13)

InChI key

YMJBYRVFGYXULK-UHFFFAOYSA-N

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Show Differences

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This Item
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&#945;-D-Glucosamine 1-phosphate

G9753

α-D-Glucosamine 1-phosphate

D-Glucosamine 6-phosphate &#8805;98% (TLC)

G5509

D-Glucosamine 6-phosphate

N,N&#8242;,N&#8242;&#8242;-Triacetylchitotriose &#8805;93% (HPLC)

T2144

N,N′,N′′-Triacetylchitotriose

2-Acetamido-2-deoxy-&#946;-D-glucopyranose 1,3,4,6-tetraacetate 98%

859990

2-Acetamido-2-deoxy-β-D-glucopyranose 1,3,4,6-tetraacetate

biological source

natural (inorganic)

biological source

natural (inorganic)

biological source

-

biological source

-

Quality Level

300

Quality Level

300

Quality Level

200

Quality Level

100

solubility

water: 100 mg/mL, clear, colorless

solubility

water: 50 mg/mL, clear to hazy, colorless to almost colorless

solubility

water: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow

solubility

-

form

powder

form

powder

form

powder

form

solid

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Application


  • Cellodextrin phosphorylase from Ruminiclostridium thermocellum: X-ray crystal structure and substrate specificity analysis. This study presents the enzymatic synthesis and analysis of alpha-ᴅ-Glucosamine 1-phosphate based polysaccharides using cellodextrin phosphorylase, showcasing potential for novel biomaterial development. Field et al., 2017

  • Glucose-1-phosphate uridylyltransferase from Erwinia amylovora: Activity, structure and substrate specificity. This paper explores the biochemical pathway involving alpha-ᴅ-Glucosamine 1-phosphate in the context of bacterial metabolism, providing insights into microbial biochemistry and potential targets for antibacterial therapy. Field et al., 2017

Other Notes

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000405319
0000340162
0000340214
0000340214
0000340162

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K Takayama et al.
The Journal of biological chemistry, 258(12), 7379-7385 (1983-06-25)
We have determined the complete structure of a glycolipid (designated lipid X) previously found to accumulate in certain Escherichia coli mutants defective in phosphatidylglycerol synthesis (Nishijima, M., and Raetz, C.R.H. (1979) J. Biol. Chem. 254, 7837-7844). Based on fast atom
F Hatzack et al.
Journal of chromatography. B, Biomedical sciences and applications, 736(1-2), 221-229 (2000-02-17)
A simple and inexpensive high-performance thin-layer chromatography (HPTLC) method for the analysis of inositol mono- to hexakisphosphates on cellulose precoated plates is described. Plates were developed in 1-propanol-25% ammonia solution-water (5:4:1) and substance quantities as low as 100-200 pmol were
D Mengin-Lecreulx et al.
The Journal of biological chemistry, 271(1), 32-39 (1996-01-05)
Two different approaches to identify the gene encoding the phosphoglucosamine mutase in Escherichia coli were used: (i) the purification to near homogeneity of this enzyme from a wild type strain and the determination of its N-terminal amino acid sequence; (ii)
Fumitaka Kudo et al.
Journal of the American Chemical Society, 127(6), 1711-1718 (2005-02-11)
Aminoglycoside antibiotics are composed of aminosugars and a unique aminocyclitol aglycon including 2-deoxystreptamine (DOS), streptidine, actinamine, etc., and nucleotidylyltransferases, sugar modifying enzymes, and glycosyltransferases appear to be essential for their biosynthesis. However, the genes encoding those enzymes were unable to
E V Vorob'eva et al.
Bioorganicheskaia khimiia, 32(5), 538-545 (2006-10-18)
The hydrolysis of defatted cells of the marine bacterium Chryseobacterium scophtalmum CIP 104199T with 10% acetic acid (3 h, 100 degrees C) led to an unusual lipid A (LA) (yield 0.6%), obtained for the first time. Using chemical analysis, FAB
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