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· · COA & SDS available for every product · Same-day shipping on in-stock items Decyl β-D-glucopyranoside - Biochemical , CAS No.58846-77-8
GRADE & PURITY Biochemical ? Biochemical grade — purity suited to biochemistry experiments and preparations. Use for enzyme, protein, and metabolic work where biocompatibility matters. Synonyms
F14799 | PLANTACARE 2000 UP | Decyl beta-D-glucopyranoside | (2R,3R,4S,5S,6R)-2-(decyloxy)-6-(hydroxymethyl)oxane-3,4,5-triol | (2R,3R,4S,5S,6R)-2-(decyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol | D5680 | DECYL GLUCOSIDE [INCI] | UNII-Z17H97EA
Shipped In
Ice chest + Ice pads
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Why this grade Biochemical Biochemical for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
F14799 | PLANTACARE 2000 UP | Decyl beta-D-glucopyranoside | (2R, 3R, 4S, 5S, 6R)-2-(decyloxy)-6-(hydroxymethyl)oxane-3, 4, 5-triol | (2R, 3R, 4S, 5S, 6R)-2-(decyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3, 4, 5-triol | D5680 | DECYL GLUCOSIDE [INCI] | UNII-Z17H97EA
Specifications & Purity
Biochemical
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 488183554 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488183554 Canonical Smiles CCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O IUPAC Name (2R,3R,4S,5S,6R)-2-decoxy-6-(hydroxymethyl)oxane-3,4,5-triol InChIKey JDRSMPFHFNXQRB-IBEHDNSVSA-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 CCCCCCCCCCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O Molecular Weight 320.4 Reaxy-Rn 35664303 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=35664303&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification 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.
3D Structure Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity Heat Sensitive Specific Rotation[α] -28° (C=C=1,MeOH) Melt Point(°C) 75 °C 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 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
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