(+)-3-Carene - ≥90% , CAS No.498-15-7

CAS: 498-15-7 Cat. No.: C303816 Formula: C₁₀H₁₆ Peso molecolare: 136.23 Numero EC: 207-856-6

GRADE & PURITY ≥90%

Synonyms

Bicyclo(4.1.0)hept-3-ene, 3,7,7-trimethyl-, (1S,6R)- | UNII-XBL40A7IA6 | EN300-198858 | (1S)-(+)-3-Carene | Q15222640 | EINECS 207-856-6 | Bicyclo(4.1.0)hept-3-ene, 3,7,7-trimethyl-, (1S)- | 15 PGJ2 | NCGC00015588-08 | (+)-3-Carene 1000 microg/mL in Isopr

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Panoramica

(1S)-(+)-3-Carene is a monoterpene.

Specifications

Sinonimi

Bicyclo(4.1.0)hept-3-ene, 3,7,7-trimethyl-, (1S,6R)- | UNII-XBL40A7IA6 | EN300-198858 | (1S)-(+)-3-Carene | Q15222640 | EINECS 207-856-6 | Bicyclo(4.1.0)hept-3-ene, 3,7,7-trimethyl-, (1S)- | 15 PGJ2 | NCGC00015588-08 | (+)-3-Carene 1000 microg/mL in Isopr

Specifiche e purezza

≥90%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged,Desiccated

Spedito in

Normal

Purezza

≥90%

Nomi e identificatori

• Pubchem Sid: 504758793
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504758793
• Sorrisi canonici: CC1=CCC2C(C1)C2(C)C
• IUPAC Name: (1S,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-3-ene
• InChIKey: BQOFWKZOCNGFEC-BDAKNGLRSA-N
• INCHI: 1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9+/m1/s1
• Isomeri SMILES: CC1=CC[C@@H]2[C@H](C1)C2(C)C
• Peso molecolare: 136.23
• Reaxy-Rn: 8141645
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8141645&ln=

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: Carane monoterpenoid - Bicyclic monoterpenoid - Branched unsaturated hydrocarbon - Polycyclic hydrocarbon - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aliphatic homopolycyclic compound
• Descrizione: 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: Bicyclic monoterpenoids

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

Proprietà chimiche e fisiche

• Solubilità: Soluble in ethanol, acetone and benzene
• Sensibilità: Air sensitive
• Indice di rifrazione: 1.47
• Rotazione specifica [α]: 14.5° (neat)
• Punto di infiammabilità (°C): 46°C(lit.)
• Punto di ebollizione (°C): 170℃
• Peso molecolare: 136.230 g/mol
• XLogP3: 2.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• 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: 186.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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

Riferimenti

1. Liu Bin, Chen Hui.  (2023)  Disruption of carboxylesterase DaEST3 reduces tolerance to host allelochemicals in Dendroctonus armandi.  Arthropod-Plant Interactions,  17  (5): (673-685).  [PMID:] [10.1007/s11829-023-09990-9]

2. Bin Liu, Hui Chen.  (2022)  Identification and Functional Characterization of the Transcription Factors AhR/ARNT in Dendroctonus armandi.  Cells,  11  (23): (3856).  [PMID:36497113] [10.3390/cells11233856]

3. Bin Liu, Danyang Fu, Hang Ning, Ming Tang, Hui Chen.  (2022)  Knockdown of CYP6CR2 and CYP6DE5 reduces tolerance to host plant allelochemicals in the Chinese white pine beetle Dendroctonus armandi.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:36127042] [10.1016/j.pestbp.2022.105180]

4. Lulu Dai, Haiming Gao, Jiaqi Ye, Danyang Fu, Yaya Sun, Hui Chen.  (2018)  Isolation of CarE genes from the Chinese white pine beetle Dendroctonus armandi (Curculionidae: Scolytinae) and their response to host chemical defense.  PEST MANAGEMENT SCIENCE,  75  (4): (986-997).  [PMID:30204286] [10.1002/ps.5205]

5. Honglei He, Feng Lan, Bei Zhang, Tianzi Gu, Jianyang Bai, Qing-He Zhang, Jacob D. Wickham, Longwa Zhang.  (2026)  Two Minus-C odorant-binding proteins (OBPs) involved in the perception of kairomone (+)-3-carene in Dendroctonus valens.  Insect Science,      [PMID:42473719] [10.1111/1744-7917.70321]

Domande frequenti

What is the purity of this product?

This product is supplied at ≥90% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature, desiccated, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 498-15-7, the molecular formula is C10H16, and the molecular weight is 136.23 g/mol. InChIKey BQOFWKZOCNGFEC-BDAKNGLRSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.