Iden­ti­fi­ca­tion

CAS Number

7512-17-6

Name

N-Acetyl-D-glu­­cosamine

Syn­onyms

N-acetyl-α-D-glu­­cosamine
2-(acetylamino)-2-deoxy-α-D-glucopyranose
233-115-1 [EINECS]
2-Acetami­­do-2-deoxy-a-D-glu­­copy­­ra­nose
2-Acetami­­do-2-deoxy-α-D-glu­­copy­­ra­nose [ACD/IUPAC Name]
2-acetami­­do-2-deoxy-α-δ-glu­­copy­­ra­nose
2-Acetami­­do-2-des­oxy-α-D-glu­­copy­­ra­nose [Ger­man] [ACD/IUPAC Name]
2-Acé­­tami­­do-2-désoxy-α-D-glu­­copy­­ra­nose [French] [ACD/IUPAC Name]
2-ace­ty­lamino-2-deoxy-a-D-glu­­copy­­ra­nose
2-ace­ty­lamino-2-deoxy-α-D-glu­­copy­­ra­nose
7512-17-6 [RN]
Glu­cosamine, N-acetyl-
MFCD00064359 [MDL num­ber]
N-((2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide
N-acetyl D-glu­­cosamine
N-acetyl-a-D-glu­­cosamine
N-ACETYL-D-GLU­­COSAMINE
N-acetyl­glu­­cosamine
N-acetyl-δ-glu­­cosamine
T13TI5GH3D
α-D-Glc­NAc
α-D-Glu­­copy­­ra­nose, 2-(acetylamino)-2-deoxy- [ACD/​Index Name]
α-Glc­NAc
α-N-Acetyl-D-glu­­cosamine
N;-acetyl-&α
N;-acetyl-&α;-D-glucosamine
??-D-Glc­NAc
??-Glc­NAc
[10036-64-3] [RN]
[6082-04-8] [RN]
2-(acetylamino)-2-deoxy-??-D-glucopyranose
2-(ACETY­LAMINO)-2-DEOXY-A-D-GLU­COPY­RA­NOSE
2-(acetylamino)-2-deoxy-A-D-glucopyranose ; 2-(acetylamino)-2-deoxy-??-D-glucopyranose ; N-acetyl-??-D-glucosamine ; ??-D-Glc­NAc ; ??-Glc­NAc
2-(acetylamino)-2-deoxy-D-glucose
2-acetami­­do-2-deoxy-α-d-glu­­copy­­ra­nose
2-ACETAMI­­DO-2-DEOXY-α-D-GLU­­COSE
6082-04-8 [RN]
95%
Acetyl Glu­cosamine
a-D-Glucopyranose,2-(acetylamino)-2-deoxy-
-D-glu­­cosamine
EINECS 233-115-1
glu­cosamine, UDP-N-acetyl-
MAG
Methyl 2-acetami­­do-2-deoxy-a-D-glu­­copy­­ra­no­side
Methyl-N-acetyl­glu­­cosamine
MFCD00056076 [MDL num­ber]
MFCD00136044 [MDL num­ber]
N-[(2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)-3-tetrahydropyranyl]acetamide
N-[(2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
N-[(2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]ethanamide
N-[(2S,3R,4R,5S,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl]acetamide
N-[(2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl]acetamide
N-[(2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-methylol-tetrahydropyran-3-yl]acetamide
N-[(2S,5S,3R,4R,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)-2H-3,4,5,6-tetrahydropy ran-3-yl]acetamide
N-[2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl]acetamide
N-acetyl-??-D-glucosamine
N-Acetyl-D-glu­­cosamine -2-H(3)
N-Acetyl-α-D-glu­­cosamine
N-Acetyl-α-D-glu­­cosaminide
NAG
NDG
PS-11249
QA-5909
SB 01966
SR-01000634877-1
UNII :T13TI5GH3D
UNII-T13TI5GH3D
WURCS=2.0/1,1,0/[a2122h-1a1-52*NCC/3=O]/1/
α-Methyl-N-Acetyl-D-Glu­­cosamine
α-N-Acetyl-D-glu­­cosamine, N-[(2S,3R,4R,5S,6R)-6-(Hydroxymethyl)-2,4,5-trihydroxytetrahydro-2H-pyran-3-yl]acetamide, 2-(Acetylamino)-2-deoxy-α-D-glucopyranose
α-N-Acetyl-D-glu­­cosamine ; N-[(2S,3R,4R,5S,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl]acetamide

SMILES

CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@@H]1O)CO)O)O

Std­InChI

InChI=1S/C8H15NO6/c1-3(11)9-5-7(13)6(12)4(2-10)15-8(5)14/h4-8,10,12-14H,2H2,1H3,(H,9,11)/t4-,5-,6-,7-,8+/m1/s1

Std­InChIKey

OVRN­­DRQM­­DR­JTHS-PVFLNQB­WSA-N

Mol­e­c­u­lar Formula

C8H15NO6

Mol­e­c­u­lar Weight

221.208

EINECS

231-368-2

MDL Number

MFCD00061615

Prop­er­ties

Appear­ance

White pow­der

Safe­ty Data

WGK Germany

3

MSDS Download

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 

Iden­ti­fi­ca­tion Methods

Assay

98%~102%

Odour

No odor

Par­ti­cle Size

≥90% through 80 Mesh

Spe­cif­ic Rotation〔α〕d20

+39.0°~+43.0°

Ph（10mg/ml）

6~8

Chlo­ride

≤0.1%

Loss On Drying

≤0.5%

Loss On Drying

≤0.5%

Residue On Ignition

≤0.1%

Iron

≤10ppm

Lead

≤10ppm

Arsenic

≤1.0ppm

Total Plate Count

≤1000CFU/​g

Yeast & Mold

≤100CFU/​g

Escherichia Coli

Not to be detected

Sal­mo­nel­la

Not to be detected

Shelf Life

2 years

Stor­age

Stored at room tem­per­a­ture for long time ; Sealed and keep away from light.

Known Appli­ca­tion

N-Acetyl­glu­­cosamine is a ver­sa­tile ingre­di­ent wide­ly used in phar­ma­ceu­ti­cals, cos­met­ics, health sup­ple­ments, and bio­med­ical mate­ri­als. Its pri­ma­ry sources include ani­mal extrac­tion and micro­bial fermentation.

In the phar­ma­ceu­ti­cal field, it helps improve joint health, pro­motes car­ti­lage matrix syn­the­sis by chon­dro­cytes, enhances car­ti­lage repair, and alle­vi­ates joint pain. As a deriv­a­tive of glu­cosamine, it sup­ports skin health and tis­sue repair.

In cos­met­ics, it stim­u­lates the syn­the­sis of hyaluron­ic acid (HA), enhanc­ing skin hydra­tion. It also repairs the skin bar­ri­er, reduc­ing red­ness and sen­si­tiv­i­ty, while accel­er­at­ing epi­der­mal cell renew­al and pro­mot­ing wound healing.

Gen­er­al View of Documents

This prod­uct is devel­oped by our R&D com­pa­ny Ulcho Bio­chem­i­cal Lim­it­ed (http://​www​.ulcho​.com/).

























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