Decyl glucoside (APG) - Moligand™, 60% in H2O , CAS No.68515-73-1

CAS: 68515-73-1 Cat. No.: T476404 Molecular Weight: 320.22 EC Number: 500-220-1

GRADE & PURITY Moligand™, 60% in H2O

Synonyms

C16H32O6 | A867031 | W-203522 | (3R,4S,5S,6R)-2-(Decyloxy)-6-(hydroxymethyl)-tetrahydro-2H-Pyran-3,4,5-triol | (3R,4S,5S,6R)-2-(Decyloxy)-6-(hydroxymethyl)tetrahydro-2H-Pyran-3,4,5-triol | D-Glucopyranoside, decyl | decyl glucopyranoside | DS-3841 | (3R,4

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

APG 0810 is a mixture of 58.0-62.0% D-glucopyranose, oligomeric, decyl octyl glycoside and 38.0-42.0% water. Contains less than 2% decanol and less than 1.0% octanol.

Specifications

Synonyms

C16H32O6 | A867031 | W-203522 | (3R, 4S, 5S, 6R)-2-(Decyloxy)-6-(hydroxymethyl)-tetrahydro-2H-Pyran-3, 4, 5-triol | (3R, 4S, 5S, 6R)-2-(Decyloxy)-6-(hydroxymethyl)tetrahydro-2H-Pyran-3, 4, 5-triol | D-Glucopyranoside, decyl | decyl glucopyranoside | DS-3841 | (3R, 4

Specifications & Purity

Moligand™, 60% in H2O

Storage

Room temperature, Argon charged

Shipped In

Normal

Grade

Moligand™

Names and Identifiers

• Canonical Smiles: CCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
• IUPAC Name: (3R,4S,5S,6R)-2-decoxy-6-(hydroxymethyl)oxane-3,4,5-triol
• InChIKey: JDRSMPFHFNXQRB-IWQYDBTJSA-N
• INCHI: 1S/C16H32O6/c1-2-3-4-5-6-7-8-9-10-21-16-15(20)14(19)13(18)12(11-17)22-16/h12-20H,2-11H2,1H3/t12-,13-,14+,15-,16?/m1/s1
• Isomeric SMILES: CCCCCCCCCCOC1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
• Molecular Weight: 320.22
• Reaxy-Rn: 35664303
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=35664303&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Fatty Acyls
      • Subclass Fatty acyl glycosides

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Fatty Acyls
• Subclass: Fatty acyl glycosides
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty acyl glycosides of mono- and disaccharides
• Alternative Parents: Hexoses Alkyl glycosides O-glycosyl compounds Oxanes Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Monosaccharide - Oxane - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. These are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.
• External Descriptors: Not available

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

Chemical and Physical Properties

• Solubility: water: freely soluble at20°C (visual)
• Molecular Weight: 320.420 g/mol
• XLogP3: 2.400
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 11
• Exact Mass: 320.22 Da
• Monoisotopic Mass: 320.22 Da
• Topological Polar Surface Area: 99.400 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 275.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• Undefined Atom Stereocenter Count: 1
• 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. Zhongjie He, Weirui Zhang, Jing Zhang, Jinliang Xie, Fangfang Su, Yuchen Li, Dongdong Yao, Yudeng Wang, Yaping Zheng.  (2024)  Enhancing the electromagnetic interference shielding of epoxy resin composites with hierarchically structured MXene/graphene aerogel.  COMPOSITES PART B-ENGINEERING,      [PMID:] [10.1016/j.compositesb.2024.111230]

2. Liangliang Ren, Lixia Zhang, Tie Geng, Jiayu Sun, Xuejian Liu, Botao Xu, Huaike Li, Lei Guo, Zhenyuan Yin.  (2025)  Impacts of Stirring Rate on CO2-in-H2O Emulsion Synthesis and Stability for Enhanced CO2 Hydrate Formation Kinetics.  ENERGY & FUELS,      [PMID:] [10.1021/acs.energyfuels.5c04813]

3. Jihao Kang, Pengyue Yu, Zhi Huang, Zhenglong Tong, Ruimin Chang, Zhiyan Xie, Shiyu Gui, Ying Huang.  (2025)  Synergistic Toxicity Reduction of Cadmium in Rice Grains by Foliar Co-Application of Nano-Silica and Surfactants.  Toxics,  13  (12): (1047).  [PMID:41441268] [10.3390/toxics13121047]

4. Liangliang Ren, Lixia Zhang, Tie Geng, Xuejian Liu, Jiayu Sun, Dnyaneshwar R. Bhawangirkar, Botao Xu, Huaike Li, Lei Guo, Zhenyuan Yin.  (2025)  Formulating liquid CO2-in-water emulsion using non-ionic surfactant alkyl polyglucoside for ultra-rapid CO2 hydrate formation.  FUEL,      [PMID:] [10.1016/j.fuel.2025.137597]