Sabinene - ≥70% , CAS No.3387-41-5

CAS: 3387-41-5 Cat. No.: S331780 Formule: C₁₀H₁₆ Poids moléculaire: 136.23 Numéro CE: 222-212-4 PubChem CID: 18818

GRADE & PURITY ≥70%

Synonyms

US Nat | C16777 | Sabinen | SABINENE, (-)-(SG) | 4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane | E75933 | EU Nat | NSC407278 | Bicyclo[3.1.0]hexane, 4-methylene-1-(1-methylethyl)- | Laurus nobilis | Black pepper | Citrus | clausena anisata | 4(10)-Thuje

Storage

Room temperature

Shipped In

Normal

Specifications

Synonymes

US Nat | C16777 | Sabinen | SABINENE, (-)-(SG) | 4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane | E75933 | EU Nat | NSC407278 | Bicyclo[3.1.0]hexane, 4-methylene-1-(1-methylethyl)- | Laurus nobilis | Black pepper | Citrus | clausena anisata | 4(10)-Thuje

Spécifications et pureté

≥70%

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥70%

Noms et identifiants

• Pubchem Sid: 504752910
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752910
• Sourires canoniques: CC(C)C12CCC(=C)C1C2
• IUPAC Name: 4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane
• InChIKey: NDVASEGYNIMXJL-UHFFFAOYSA-N
• INCHI: 1S/C10H16/c1-7(2)10-5-4-8(3)9(10)6-10/h7,9H,3-6H2,1-2H3
• Isomères SMILES: CC(C)C12CCC(=C)C1C2
• PubChem CID: 18818
• Poids moléculaire: 136.23

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Prenol lipids
      • Subclass Monoterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Bicyclic monoterpenoids
• Alternative Parents: Polycyclic hydrocarbons Branched unsaturated hydrocarbons Cyclic olefins Unsaturated aliphatic hydrocarbons
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Bicyclic monoterpenoid - Thujane monoterpenoid - Branched unsaturated hydrocarbon - Polycyclic hydrocarbon - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aliphatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
• External Descriptors: a monoterpenoid

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

Cibles associées (non humaines)

Pyricularia grisea (1253 Activities)

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

Phytophthora infestans (820 Activities)

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Puccinia recondita (281 Activities)

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Blumeria graminis (462 Activities)

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Botrytis cinerea (4183 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Point d'ébullition (°C): 163-164° C at 760 mmHg
• Poids moléculaire: 136.230 g/mol
• XLogP3: 3.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 136.125 Da
• Monoisotopic Mass: 136.125 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 178.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• 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. Zefu Wang, Zhifei He, Dong Zhang, Xiaosi Chen, Hongjun Li.  (2021)  The effect of linalool, limonene and sabinene on the thermal stability and structure of rabbit meat myofibrillar protein under malondialdehyde-induced oxidative stress.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2021.111707]

2. Yuchen Bai, Ningke You, Hongyu Tian, Xuebing Zhao.  (2025)  Characterization of Key Odorants in Hemp Seed Oil Extracted from the Hemp Seeds Roasted Under Various Conditions.  Processes,  13  (2): (530).  [PMID:] [10.3390/pr13020530]

3. Yan Yan Lin, Min Xing Zhang, Miao Sun, Lu Sheng Wan, You Zhou, Jing Sheng Chen.  (2024)  Discovering potential fumigants against Tribolium castaneum from essential oils using GC-MS and chemometric approaches.  JOURNAL OF STORED PRODUCTS RESEARCH,      [PMID:] [10.1016/j.jspr.2024.102485]

4. Huanyan Liang, Feifei Lv, Mengting Xian, Chenghua Luo, Lei Zhang, Meihua Yang, Qian Li, Xiangsheng Zhao.  (2025)  Inhibition Mechanism of Cinnamomum burmannii Leaf Essential Oil Against Aspergillus flavus and Aflatoxins.  Foods,  14  (4): (682).  [PMID:40002124] [10.3390/foods14040682]