Methyl 3-hydroxydecanoate - ≥98% , CAS No.62675-82-5

CAS: 62675-82-5 Cat. No.: M274751 Formule: C₁₁H₂₂O₃ Poids moléculaire: 202.29

GRADE & PURITY ≥98%

Synonyms

SB50162 | Methyl ester of 3-hydroxydecanoic acid | 3-hydroxy Decanoic Acid methyl ester | FT-0669510 | r-(3)-Hydroxydecanoic acid,methyl ester | Methyl 3-hydroxydecanoate # | DL-2-HYDROXYDECANOICACIDMETHYLESTER | FT-0695823 | PD077431 | rac 3-Hydroxydecan

Storage

Store at -20°C,Argon charged,Desiccated

Shipped In

Ice chest + Ice pads

Application

Drug Delivery, Surface Modification, PEGylation of Protein, Peptide & Oligo

Specifications

Synonymes

SB50162 | Methyl ester of 3-hydroxydecanoic acid | 3-hydroxy Decanoic Acid methyl ester | FT-0669510 | r-(3)-Hydroxydecanoic acid,methyl ester | Methyl 3-hydroxydecanoate # | DL-2-HYDROXYDECANOICACIDMETHYLESTER | FT-0695823 | PD077431 | rac 3-Hydroxydecan

Spécifications et pureté

≥98%

Mécanismes biochimiques et physiologiques

3-Hydroxy fatty acid methyl ester. For use as standard and possible use in biological systems.

Conditions de stockage de stockage

Store at -20°C,Argon charged,Desiccated

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥98%

Noms et identifiants

• Sourires canoniques: CCCCCCCC(CC(=O)OC)O
• IUPAC Name: methyl 3-hydroxydecanoate
• InChIKey: UBVACUZVNTVHTE-UHFFFAOYSA-N
• INCHI: 1S/C11H22O3/c1-3-4-5-6-7-8-10(12)9-11(13)14-2/h10,12H,3-9H2,1-2H3
• Isomères SMILES: CCCCCCCC(CC(=O)OC)O
• Poids moléculaire: 202.29
• Reaxy-Rn: 1770390
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1770390&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Fatty Acyls
      • Subclass Fatty alcohols

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Fatty Acyls
• Subclass: Fatty alcohols
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty alcohols
• Alternative Parents: Fatty acid methyl esters Beta hydroxy acids and derivatives Methyl esters Secondary alcohols Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty alcohol - Beta-hydroxy acid - Fatty acid ester - Fatty acid methyl ester - Hydroxy acid - Methyl ester - Carboxylic acid ester - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
• 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

Propriétés chimiques et physiques

• Solubilité: Soluble in ethanol
• Poids moléculaire: 202.290 g/mol
• XLogP3: 2.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 9
• Exact Mass: 202.157 Da
• Monoisotopic Mass: 202.157 Da
• Topological Polar Surface Area: 46.500 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 145.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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

Références

1. Weiqiang Wang, Weifeng Zhang, Fengjiao Chu, Tingting Xiao, Dongdong Hu, Pengyi Tang, Jiajia Gao, Honghua Ge.  (2025)  An engineered living biofilm system for sustainable conversion of CO2 into polyhydroxyalkanoates.  Cell Reports Physical Science,      [PMID:] [10.1016/j.xcrp.2025.102676]