γ-Decanolactone - 10mM in DMSO , CAS No.706-14-9

CAS: 706-14-9 Cat. No.: D425612 Formule: C₁₀H₁₈O₂ Poids moléculaire: 170.25 Numéro CE: 211-892-8

GRADE & PURITY 10mM in DMSO

Synonyms

Decanolide-1,4 | Hydroxydecanoic acid, gamma-lactone | 5-Hexyl-dihydro-furan-2-one | Decanoic acid, gamma-lactone | .gamma.-Decanolide | 4-Hexyl-.gamma.-butyrolactone | gamma-Decalactone, >=98%, FCC, FG | NSC 26510 | Q423956 | UNII-7HLS05KP9O | gamma-N-He

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Synonymes

Decanolide-1,4 | Hydroxydecanoic acid, gamma-lactone | 5-Hexyl-dihydro-furan-2-one | Decanoic acid, gamma-lactone | .gamma.-Decanolide | 4-Hexyl-.gamma.-butyrolactone | gamma-Decalactone, >=98%, FCC, FG | NSC 26510 | Q423956 | UNII-7HLS05KP9O | gamma-N-He

Spécifications et pureté

10mM in DMSO

Conditions de stockage de stockage

Store at -80°C

Expédié en

Dry ice packs + Cold packs

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

Noms et identifiants

• Pubchem Sid: 528769191
• Sourires canoniques: CCCCCCC1CCC(=O)O1
• IUPAC Name: 5-hexyloxolan-2-one
• InChIKey: IFYYFLINQYPWGJ-UHFFFAOYSA-N
• INCHI: 1S/C10H18O2/c1-2-3-4-5-6-9-7-8-10(11)12-9/h9H,2-8H2,1H3
• Isomères SMILES: CCCCCCC1CCC(=O)O1
• WGK Allemagne: 1
• RTECS: LU4600000
• Poids moléculaire: 170.25
• Reaxy-Rn: 117547
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=117547&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Lactones
      • Subclass Gamma butyrolactones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Lactones
• Subclass: Gamma butyrolactones
• Intermediate Tree Nodes: Not available
• Direct Parent: Gamma butyrolactones
• Alternative Parents: Tetrahydrofurans Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Gamma butyrolactone - Tetrahydrofuran - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as gamma butyrolactones. These are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.
• 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

Mécanismes d'action

Propriétés chimiques et physiques

• Indice de réfraction: 1.4488
• Point d'éclair (°F): 276.8 °F
• Point d'éclair (°C): 113 °C
• Point d'ébullition (°C): 281°C
• Poids moléculaire: 170.250 g/mol
• XLogP3: 2.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 170.131 Da
• Monoisotopic Mass: 170.131 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 143.000
• 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. Xuewei Jia, Yuan Gao, Hui Xi, Chun Cui, Xiao Yang, Baojiang He, Chunping Xu, Mingqi Gao, Tianxiao Li.  (2025)  A flavor imitation method for Osmanthus aroma based on molecular docking screening and odor activity value analysis.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2025.117697]