WARNING: This product is for research use only, not for human or veterinary use.
MedKoo CAT#: 462154
Description: Jasmolin I is an active insecticidal constituent of pyrethrum flowers.
MedKoo Cat#: 462154
Name: Jasmolin I
Chemical Formula: C21H32O3
Exact Mass: 332.2351
Molecular Weight: 332.484
Elemental Analysis: C, 75.86; H, 9.70; O, 14.44
This product is not in stock, which may be available by custom synthesis.
For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge).
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Synonym: Jasmolin I
IUPAC/Chemical Name: (1S)-2-methyl-4-oxo-3-((Z)-pent-2-en-1-yl)cyclopentyl (3R)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropane-1-carboxylate
InChi Key: GPVJMMOTPLDBPJ-ZZRSPYMPSA-N
InChi Code: InChI=1S/C21H32O3/c1-7-8-9-10-15-14(4)18(12-17(15)22)24-20(23)19-16(11-13(2)3)21(19,5)6/h8-9,11,14-16,18-19H,7,10,12H2,1-6H3/b9-8-/t14?,15?,16-,18+,19?/m1/s1
SMILES Code: CC/C=C\CC1C(C)[C@@H](OC(C2C(C)(C)[C@@H]2/C=C(C)\C)=O)CC1=O
Appearance: Solid powder
Purity: >98% (or refer to the Certificate of Analysis)
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility: Soluble in DMSO
Shelf Life: >3 years if stored properly
Drug Formulation: This drug may be formulated in DMSO
Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code: 2934.99.9001
The following data is based on the product molecular weight 332.484 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
|Concentration / Solvent Volume / Mass||1 mg||5 mg||10 mg|
|1 mM||1.15 mL||5.76 mL||11.51 mL|
|5 mM||0.23 mL||1.15 mL||2.3 mL|
|10 mM||0.12 mL||0.58 mL||1.15 mL|
|50 mM||0.02 mL||0.12 mL||0.23 mL|
1: Dissipation and Residues of Pyrethrins in Leaf Lettuce under Greenhouse and Open Field Conditions Lixiang Pan, Xiaoxiao Feng, Hongyan Zhang Int J Environ Res Public Health. 2017 Jul; 14(7): 822. Published online 2017 Jul 21. doi: 10.3390/ijerph14070822 PMCID: PMC5551260
2: Augmentation of pyrethrins content in callus of Chrysanthemum cinerariaefolium and establishing its insecticidal activity by molecular docking of NavMS Sodium Channel Pore receptor M. Paramesha, S. Manivannan, S. J. Aditya Rao, K. S. Srikanth, Bhagyalakshmi Neelwarne, Nandini P. Shetty 3 Biotech. 2018 Aug; 8(8): 367. Published online 2018 Aug 10. doi: 10.1007/s13205-018-1387-8 PMCID: PMC6086810
3: Jasmone Hydroxylase, a Key Enzyme in the Synthesis of the Alcohol Moiety of Pyrethrin Insecticides Wei Li, Fei Zhou, Eran Pichersky Plant Physiol. 2018 Aug; 177(4): 1498–1509. Published online 2018 Jul 2. doi: 10.1104/pp.18.00748 PMCID: PMC6084660
4: Pyrethrin Biosynthesis: The Cytochrome P450 Oxidoreductase CYP82Q3 Converts Jasmolone To Pyrethrolone Wei Li, Daniel B. Lybrand, Fei Zhou, Robert L. Last, Eran Pichersky Plant Physiol. 2019 Nov; 181(3): 934–944. Published online 2019 Aug 26. doi: 10.1104/pp.19.00499 PMCID: PMC6836846
5: Comparative transcriptome analysis reveals candidate genes for the biosynthesis of natural insecticide in Tanacetum cinerariifolium Sana Khan, Swati Upadhyay, Feroz Khan, Sudeep Tandon, Rakesh Kumar Shukla, Sumit Ghosh, Vikrant Gupta, Suchitra Banerjee, Laiq ur Rahman BMC Genomics. 2017; 18: 54. Published online 2017 Jan 9. doi: 10.1186/s12864-016-3409-4 PMCID: PMC5220608