Molecular structure of (−)-β-Pinene, CAS Number: 18172-67-3
(−)-β-Pinene (CAS 18172-67-3)
Alternate Names:
(1S,5S)-6,6-Dimethyl-2-methylenebicyclo
Application:
(−)-β-Pinene is a useful biochemical for proteomics research
CAS Number:
18172-67-3
Purity:
≥98%
Molecular Weight:
136.23
Molecular Formula:
C10H16
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
(−)-β-Pineneis a useful biochemical for proteomics research. (−)-β-Pinene is a prevalent monoterpene found in the essential oils of numerous plants. Although the precise mechanism of action of (−)-β-Pinene remains partially elusive, it is thought to exert its effects by hindering the synthesis of inflammatory mediators like prostaglandins and leukotrienes. Additionally, it is believed to influence the activity of neurotransmitters, including dopamine and acetylcholine
(−)-β-Pinene (CAS 18172-67-3) References
- Cloning and functional characterization of a beta-pinene synthase from Artemisia annua that shows a circadian pattern of expression. | Lu, S., et al. 2002. Plant Physiol. 130: 477-86. PMID: 12226526
- The microbial oxidation of (-)-beta-pinene by Botrytis cinerea. | Farooq, A., et al. 2002. Z Naturforsch C J Biosci. 57: 686-90. PMID: 12240997
- Biotransformation of (-)beta-pinene by Aspergillus niger ATCC 9642. | Toniazzo, G., et al. 2005. Appl Biochem Biotechnol. 121-124: 837-44. PMID: 15930563
- Dual stereoselectivity in the dialkylzinc reaction using (-)-beta-pinene derived amino alcohol chiral auxiliaries. | Binder, CM., et al. 2009. J Org Chem. 74: 2337-43. PMID: 19216500
- Optimization of α-Terpineol production by the biotransformation of R-(+)-limonene and (-)-β-pinene. | Rottava, I., et al. 2011. Appl Biochem Biotechnol. 164: 514-23. PMID: 21234702
- Comparative anti-infectious bronchitis virus (IBV) activity of (-)-pinene: effect on nucleocapsid (N) protein. | Yang, Z., et al. 2011. Molecules. 16: 1044-54. PMID: 21350392
- Biosynthesis of monoterpenes. Stereochemistry of the enzymatic cyclizations of geranyl pyrophosphate to (+)-alpha-pinene and (-)-beta-pinene. | Croteau, R., et al. 1989. J Biol Chem. 264: 2075-80. PMID: 2644252
- One-pot synthesis and antimicrobial evaluation of novel 3-cyanopyridine derivatives of (-)-β-pinene. | Liao, S., et al. 2016. Bioorg Med Chem Lett. 26: 1512-1515. PMID: 26898336
- Characterization and Antihypertensive Effect of the Complex of (-)-β- pinene in β-cyclodextrin. | Moreira, IJ., et al. 2016. Curr Pharm Biotechnol. 17: 837-45. PMID: 27109904
- Hydronopylformamides: Modification of the Naturally Occurring Compound (-)-β-Pinene to Produce Insect Repellent Candidates against Blattella germanica. | Liao, S., et al. 2017. Molecules. 22: PMID: 28621730
- De novo Transcriptome Characterization of Rhodomyrtus tomentosa Leaves and Identification of Genes Involved in α/β-Pinene and β-Caryophyllene Biosynthesis. | He, SM., et al. 2018. Front Plant Sci. 9: 1231. PMID: 30197651
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
(−)-β-Pinene, 5 ml | sc-250724 | 5 ml | $38.00 | |||
(−)-β-Pinene, 250 ml | sc-250724A | 250 ml | $77.00 |