Methyl α-D-glucopyranoside - Moligand™, ≥98% , CAS No.97-30-3

CAS: 97-30-3 Cat. No.: M106708 Molecular Weight: 194.18 Beilstein Registry Number: 81568 EC Number: 202-571-3

GRADE & PURITY Moligand™, ≥98%

Synonyms

METHYL .ALPHA.-D-(+)-GLUCOSIDE | Methyl alpha-D-glucopyranoside, for microbiology, >=99.0% | alpha-D-methyl glucoside | .alpha.-Methyl-(d)-glucoside | 1ws4 | alpha-methyl-D-glucopyranoside (AMG) | alpha-Methyl-D-glucoside | Q27074402 | EN300-92952 | Malph

Storage

Room temperature,Argon charged,Cool

Shipped In

Normal

Specifications

Synonyms

METHYL .ALPHA.-D-(+)-GLUCOSIDE | Methyl alpha-D-glucopyranoside, for microbiology, >=99.0% | alpha-D-methyl glucoside | .alpha.-Methyl-(d)-glucoside | 1ws4 | alpha-methyl-D-glucopyranoside (AMG) | alpha-Methyl-D-glucoside | Q27074402 | EN300-92952 | Malph

Specifications & Purity

Moligand™, ≥98%

Storage

Room temperature, Argon charged, Cool

Shipped In

Normal

Grade

Moligand™

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504753933
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504753933
• Canonical Smiles: COC1C(C(C(C(O1)CO)O)O)O
• IUPAC Name: (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-methoxyoxane-3,4,5-triol
• InChIKey: HOVAGTYPODGVJG-ZFYZTMLRSA-N
• INCHI: 1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6-,7+/m1/s1
• Isomeric SMILES: CO[C@@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
• WGK Germany: 3
• Molecular Weight: 194.18
• Beilstein: 81568
• Reaxy-Rn: 1681114
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1681114&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Glycosyl compounds
          • Level6 O-glycosyl compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: O-glycosyl compounds
• Alternative Parents: Oxanes Monosaccharides Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: O-glycosyl compound - Oxane - Monosaccharide - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.
• External Descriptors: alpha-D-glucoside - methyl D-glucoside

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

PYGB Tchem Brain glycogen phosphorylase (474 Activities)

Discover Target: PYGB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

Discover Target: TP53

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HeLa (62764 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in water. Insoluble in ether
• Sensitivity: Air & Moisture Sensitive
• Specific Rotation[α]: 157.5 ° (C=10, H2O)
• Boil Point(°C): 200°C
• Melt Point(°C): 170°C
• Molecular Weight: 194.180 g/mol
• XLogP3: -2.200
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 194.079 Da
• Monoisotopic Mass: 194.079 Da
• Topological Polar Surface Area: 99.400 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 163.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Ronghua Zhang, Wenhao Zhang, Jianchun Jiang, Junming Xu, Kui Wang, Junfeng Feng, Hui Pan.  (2023)  Catalytic valorization of biomass carbohydrates into levulinic acid/ester by using bifunctional catalysts.  RENEWABLE ENERGY,      [PMID:] [10.1016/j.renene.2023.119851]

2. Zhou Lipeng, Gao Dongting, Yang Jingru, Yang Xiaomei, Su Yunlai, Lu Tianliang.  (2019)  Conversion of recalcitrant cellulose to alkyl levulinates and levulinic acid via oxidation pretreatment combined with alcoholysis over Al2(SO4)3.  CELLULOSE,  27  (3): (1451-1463).  [PMID:] [10.1007/s10570-019-02903-1]

3. Qiying Liu, Haiyong Wang, Haosheng Xin, Chenguang Wang, Long Yan, Yingxiong Wang, Qi Zhang, Xinghua Zhang, Ying Xu, George W. Huber, Longlong Ma.  (2019)  Selective Cellulose Hydrogenolysis to Ethanol Using Ni@C Combined with Phosphoric Acid Catalysts.  ChemSusChem,  12  (17): (3977-3987).  [PMID:31225696] [10.1002/cssc.201901110]

4. Xuzhao Yang, Jun Wang, Hao Song, Wenyuan Zou.  (2015)  Thermal properties and solubility of methyl α-d-glucopyranoside in methanol at different temperatures.  FLUID PHASE EQUILIBRIA,      [PMID:] [10.1016/j.fluid.2015.10.047]

5. Zhen Ma, Jingyang Zhang, Yucheng Lin, Xiuli Han, Haoran Wu, Chunbao Xu, Chun Chang.  (2025)  Alcoholysis of High-Solid xylose residue for methyl levulinate preparation and its kinetics.  BIORESOURCE TECHNOLOGY,      [PMID:39814150] [10.1016/j.biortech.2025.132063]

6. Xiangbiao Li, Hu Li, Qingmei Ge, Wenfeng Zhao, Hang Cong.  (2025)  Bimetallic synergy in tin-modified zeolites for highly efficient conversion of cellulose to methyl levulinate.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.138198]