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N-Acetylglucosamine

N-Acetylglucosamine Suppliers list
Company Name: airuikechemical co., ltd.
Tel: +undefined86-15315557071
Email: sales02@airuikechemical.com
Products Intro: Cas:7512-17-6
ProductName:acetylglucosamine
Purity: 99.9%|Package: 1Kg;0.00;USD|5Kg;0.00;USD|25Kg;0.00;USD
Company Name: Chengdu Peter-like Biotechnology Co., Ltd.  
Tel: 028-81700200 18108052721
Email: 2850505130@qq.com
Products Intro: Cas:7512-17-6
ProductName:N-Acetylglucosamine
Purity: HPLC>=98% | Package: 20mg mg/
Company Name: Huzhou Chenxi Environmental Protection Technology Co. , Ltd.
Tel: +8616762203950
Email: 1034385273@qq.com
Products Intro: Cas:7512-17-6
ProductName:N-Acetyl glucoasamine
Purity: 99% | Package: 25KG
Company Name: Shanghai Hao Zhun Biological Technology Co., Ltd.  
Tel: 15800340161 15800340161
Email: info@zzsrm.com
Products Intro: Cas:7512-17-6
ProductName:N-Acetylglucosamine (200 mg)
Purity: 98.0%
Company Name: Riedel-de Haen AG
Tel: 800 558-9160
Email:
Products Intro: Cas:7512-17-6
ProductName:N-Acetylglucosamine
Brand: Sigma-Aldrich | Product Number: PHR1432 | Purity: Pharmaceutical Secondary Standard; Certified Reference Material

N-Acetylglucosamine manufacturers

  • acetylglucosamine
  • acetylglucosamine pictures
  • $0.00 / 1Kg
  • 2024-10-15
  • CAS:7512-17-6
  • Min. Order: 1Kg
  • Purity: 99.9%
  • Supply Ability: 200tons

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N-Acetylglucosamine Basic information
Product Name:N-Acetylglucosamine
Synonyms: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
CAS:7512-17-6
MF:C8H15NO6
MW:221.21
EINECS:231-368-2
Product Categories:Dextrins、Sugar & Carbohydrates;Biochemistry;Glucose;Sugars;13C & 2H Sugars;Biological and chemical;Carbohydrate Matrices;Affinity Chromatography;Protein Chromatography;aldehydes;Carbohydrates & Derivatives;Aminosugars;amino;bc0001;Glycon Biochem;7512-17-6
Mol File:7512-17-6.mol
N-Acetylglucosamine Structure
N-Acetylglucosamine Chemical 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
pKa13.04±0.20(Predicted)
color white to off-white
optical activityAlpha 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.
InChIKeyOVRNDRQMDRJTHS-ROGOILFBSA-N
LogP-2.2 at 23.7℃
CAS DataBase Reference7512-17-6(CAS DataBase Reference)
EPA Substance Registry SystemN-Acetylglucosamine (7512-17-6)
Safety Information
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
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
N-Acetylglucosamine Usage And Synthesis
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).

N-Acetylglucosamine Preparation Products And Raw materials
Preparation ProductsBENZYL 2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE-->D(+)-Glucose
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