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N-Acetylglucosamine

CAS No.
7512-17-6
Chemical Name:
N-Acetylglucosamine
Synonyms
N-ACETYLGLUCOSAMINE;D-GLCNAC;acetylglucosamine;2-Acetamido-2-deoxy-D-glucopyranose;Acetyl chitin;N-Acetyl-D-glucosamin;N-ACETYL-D-GLUCOSAMINIDE;N-Acetyl-beta-D-glucosamine;2-ACETAMIDO-2-DEOXY-D-GLUCOSE;NADG
CBNumber:
CB00125841
Molecular Formula:
C8H15NO6
Molecular Weight:
221.21
MDL Number:
MFCD00136044
MOL File:
7512-17-6.mol
MSDS File:
SDS
Last updated:2024-12-18 13:37:16

N-Acetylglucosamine Properties

Melting point 211 °C (dec.) (lit.)
alpha 42 º (c=2,water,2 hrs)
vapor pressure 8Pa at 20℃
refractive index +39.0 to +42.0 ° (C=1, H2O)
storage temp. -20°C
solubility Soluble in concentrated hydrochloric acid, sulfuric acid, phosphoric acid and formic acid. Insoluble in water, dilute acids, dilute alkalis, concentrated alkalis and organic solvents.
form saline suspension
Boiling point 636.4±55.0 °C(Predicted)
Density 1.54 g/cm3
pka 13.04±0.20(Predicted)
color white to off-white
optical activity Alpha type +75 → +41 Beta type -22 → +41.3
Water Solubility H2O: 50 mg/mL colorless to faint yellow solution, clear to very slightly hazy
Sensitive Hygroscopic
Merck 14,4458
BRN 1727589
Stability Stable. Incompatible with strong oxidizing agents.
InChIKey OVRNDRQMDRJTHS-ROGOILFBSA-N
LogP -2.2 at 23.7℃
CAS DataBase Reference 7512-17-6(CAS DataBase Reference)
FDA UNII V956696549
EPA Substance Registry System N-Acetylglucosamine (7512-17-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P280-P305+P351+P338-P310
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  24/25-36-26-22
WGK Germany  3
RTECS  LZ6651000
3-10
Hazard Note  Irritant
TSCA  Yes
HS Code  29329985
NFPA 704
1
0 0

N-Acetylglucosamine price More Price(79)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich A3286 N-Acetyl-D-glucosamine suitable for cell culture, BioReagent 7512-17-6 5g $36.1 2024-03-01 Buy
Sigma-Aldrich 1010022 N-Acetyl-D-glucosamine United States Pharmacopeia (USP) Reference Standard 7512-17-6 200mg $383 2024-03-01 Buy
TCI Chemical A0092 N-Acetyl-D-glucosamine >98.0%(HPLC)(N) 7512-17-6 25g $37 2024-03-01 Buy
TCI Chemical A0092 N-Acetyl-D-glucosamine >98.0%(HPLC)(N) 7512-17-6 100g $106 2024-03-01 Buy
Alfa Aesar A13047 N-Acetyl-D-glucosamine, 98+% 7512-17-6 10g $28.8 2023-06-20 Buy
Product number Packaging Price Buy
A3286 5g $36.1 Buy
1010022 200mg $383 Buy
A0092 25g $37 Buy
A0092 100g $106 Buy
A13047 10g $28.8 Buy

N-Acetylglucosamine Chemical Properties,Uses,Production

Cell Structure Components

N-Acetylglucosamine (GlcNAc) is a key component of bacterial cell wall peptidoglycan, fungal cell wall chitin, and animal cell extracellular matrix, and plays an important structural role on the cell surface. It has been shown that GlcNAc has a novel role in cell signalling that stimulates morphological changes and virulence gene expression in the human fungal pathogen Candida albicans. Pathogenic Escherichia coli responds to GlcNAc by altering the expression of cilia and CURLI fibres that promote biofilm formation. Studies in animal cells have shown that GlcNAc affects cell signalling by post-translational modification of proteins through glycosylation.The O-bonding of GlcNAc to Ser and Thr residues regulates a wide range of intracellular proteins, including transcription factors such as NFκB, c-myc and p53. In addition, the specificity of the Notch family of receptors for different ligands is altered by GlcNAc attachment to fucose residues in the extracellular structural domain.GlcNAc also affects cell surface signalling proteins by altering the degree of branching of N-linked glycans that influence signal transduction.
N-Acetylglucosamine.png

Uses

N-Acetylglucosamine (GlcNAc) is widely used as a nutritional supplement to aid joint health and treat osteoarthritis. In addition, GlcNAc also plays a key role in cell signalling, similar to other common types of messenger molecules, including ions, nucleotides and amino acids. Studies have shown GlcNAc to have beneficial therapeutic effects in patients with inflammatory bowel disease.

Mechanism of action

The mechanism of action in relieving arthritic pain and in repair of cartilage is a matter of speculation. Biochemically, glucosamine is involved in glycoprotein metabolism. Glycoproteins, known as proteoglycans, form the ground substance in the extra-cellular matrix of connective tissue. Proteoglycans are polyanionic substances of high-molecular weight and contain many different types of heteropolysaccharide side-chains covalently linked to a polypeptide-chain backbone. These polysaccharides make up to 95% of the proteoglycan structure. In fact, chemically, proteoglycans resemble polysaccharides more than they do proteins. The polysaccharide groups in proteoglycans are called glycosaminoglycans (GAGs). GAGs include hyaluronic acid, chondroitin sulfate, dermatan sulfate, keratan sulfate, heparin and heparan sulfate. All of the GAGs contain derivatives of glucosamine or galactosamine. Glucosamine derivatives are found in hyaluronic acid, keratan sulfate and heparan sulfate. Chondroitin sulfate contains derivatives of galactosamine. The glucosamine-containing glycosaminoglycan hyaluronic acid is vital for the function of articular cartilage. GAG chains are fundamental components of aggrecan found in articular cartilage. Aggrecan confers upon articular cartilage shock-absorbing properties. It does this by providing cartilage with a swelling pressure that is restrained by the tensile forces of collagen fibers. This balance confers upon articular cartilage the deformable resilience vital to its function. In the early stages of degenerative joint disease, aggrecan biosynthesis is increased. However, in later stages, aggrecan synthesis is decreased, leading eventually to the loss of cartilage resiliency and to most of the symptoms that accompany osteoarthritis. During the progression of osteoarthritis, exogenous glucosamine may have a beneficial role. It is known that, in vitro, chondrocytes do synthesize more aggregan when the culture medium is supplemented with glucosamine. N-acetylglucosamine is found to be less effective in these in vitro studies. Glucosamine has also been found to have antioxidant activity and to be beneficial in animal models of experimental arthritis. The counter anion of the glucosamine salt (i.e. chloride or sulfate) is unlikely to play any role in the action or pharmacokinetics of glucosamine. Further, the sulfate in glucosamine sulfate supplements should not be confused with the glucosamine sulfate found in such GAGs as keratan sulfate and heparan sulfate. In the case of the supplement, sulfate is the anion of the salt. In the case of the above GAGs, sulfate is present as an ester. Also, there is no glucosamine sulfate in chondroitin sulfate (source: PDRhealth).

108-24-7
66-84-2
7512-17-6
Synthesis of N-Acetylglucosamine from Acetic anhydride and D-Glucosamine hydrochloride

N-Acetylglucosamine Preparation Products And Raw materials

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View Lastest Price from N-Acetylglucosamine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
acetylglucosamine pictures 2024-12-24 acetylglucosamine
7512-17-6
US $0.00-0.00 / Kg 1Kg 99.9% 200tons airuikechemical co., ltd.
N-acetylgalactosaminyl-1-4-N-acetylglucosamine pictures 2024-12-13 N-acetylgalactosaminyl-1-4-N-acetylglucosamine
136198-41-9
US $0.00 / G 10G 98%min 30kg/month WUHAN FORTUNA CHEMICAL CO., LTD
N-Acetyl-D-Glucosamine;N-Acetylglucosamine pictures 2024-05-09 N-Acetyl-D-Glucosamine;N-Acetylglucosamine
7512-17-6
US $0.00 / kg 1kg 99% 10000kg Shaanxi TNJONE Pharmaceutical Co., Ltd
N-Acetyl-D-glucosaMine, 98.0%(LC&N N-qcetyl-D-glucosamine 2-Acetamido-2-deoxy-alpga-D-glucopyranose ACETYL-D-GLUCOSAMINE, N- N-ACETYL-DELTA-GLUCOSAMINE 2-ACETAMIDO-2-DESOXY-D-GLUCOPYRANOSE, N-ACETYL-D-GLUCOSAMINE 2-AcetaMido-2-deoxy-D-glucopyranose, 98% 10GR N-ACETYL-D-GLUCOSAMINE 80 MESH N-ACETYL-D-GLUCOSAMINE CELL CULTURETESTE D N-Acetyl-D-Glucosamine97.5-102.5% N-Acetylglucosamine,USP28:97,5-102,5%HPLC NSC 52434 D-Glucose, 2-(acetylamino)-2-deoxy- N-[(3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide N-ACETYL-D-GLUCOSAMINE COSMETIC GRADE 2-Acetamido-2-deoxy-D-glucopyranose, N-Acetyl-D-glucosamine N-((1R,2R,3S,4R)-1-FORMYL-2,3,4,5-TETRAHYDROXY-PENTYL)-ACETAMIDE N-ACETYL-D-GLUCOSAMINE, IMMOBILIZED ON DIVINYLSULFONE-ACTIVATED AGAROSE 6B 2-(acetylamino)-2-deoxy-d-glucos N-Acety-D-GlucosaMine N-ACETYLGLUCOSAMINE (13C6, 99%) N-Acetylglucosamine (200 mg) N-Acetyl-D-glucosamine (NADG) N- acetyl -D- glucosamine (N- acetylglucosamine) 2-Acetamido-2-deoxy-D-glucose 2-Acetamido-2-deoxy-D-glucopyranose N-Acetyl-D-glucosamine N-[2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl]acetamide D-GlcNAc 2-Acetanido-2-deoxy-α-D-glucopyranose N-Acetamideo-2-deoxy-D-glucose N-acetyl-D-glucosamine;2-Acetanido-2-deoxy-α-D-glucopyranose;N-Acetamideo-2-deoxy-D-glucose;D-GlcNAc 2-Acetamido-2-deoxy-D-glucoseN-Acetyl-beta-D-glucosamine N-Acetyl-D-glucosamine, N-[(1R,2R,3S,4R)-1-Formyl-2,3,4,5-tetrahydroxypentyl]acetamide NSC 524344 N-Acetyl-D-glucosamine, 98+% 2-Acetamido-2-deoxy-alpha-glucopyranose N-ACETYL-D-GLUCOSAMINE extrapure AR for biochemistry 2-Acetamido-2-deoxy-D-glucose, D-GlcNAc 2-Acetamido-2-deoxyglucose 2-Acetamido-D-glucose D-N-Acetylglucosamine 2-(acetylamino)-2-deoxy-D-Glucose 2-Acetamido-2-deoxy-D-glucopyranose,98% N-Acetyl-D-glucosamine ACETYL-DL-GLUCOSAMINE, N-(P) N-Acetyl-D-glucosamine,2-Acetamido-2-deoxy-D-glucose, D-GlcNAc N-Acetyl-D-glucosami NADG ACEN-001 N-Acetyl-D-glucosamine - plant source Glucosamine Impurity A 2-Acetamido-2-deoxy-D-glucose 95% N-Acetyl-D-glucosamine - CAS 7512-17-6 - Calbiochem Gastrodin Impurity 9 N-((1S,2R,3R,4R)-2,3,6-trihydroxy N-Acetyl-D-glucosamine > Marine Sweet N-Acetyl-2-amino-2-deoxy-D-glucose N-Acetyl-2-amino-2-deoxyglucose N-Acetyl-D-Glucosamine USP/EP/BP N-acetyl-α-D-glucosamine