MedKoo Cat#: 598479 | Name: Lavandulyl acetate

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Lavandulyl acetate is the acetate ester of lavandulol. It is a component of lavender oil.

Chemical Structure

Lavandulyl acetate
Lavandulyl acetate
CAS#20777-39-3

Theoretical Analysis

MedKoo Cat#: 598479

Name: Lavandulyl acetate

CAS#: 20777-39-3

Chemical Formula: C12H20O2

Exact Mass: 196.1463

Molecular Weight: 196.29

Elemental Analysis: C, 73.43; H, 10.27; O, 16.30

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Synonym
Lavandulyl acetate; (R)-Lavandulyl acetate; (-)-Lavandulyl acetate; (-)-(R)-Lavandulyl acetate;
IUPAC/Chemical Name
(R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl acetate
InChi Key
HYNGAVZPWWXQIU-LBPRGKRZSA-N
InChi Code
InChI=1S/C12H20O2/c1-9(2)6-7-12(10(3)4)8-14-11(5)13/h6,12H,3,7-8H2,1-2,4-5H3/t12-/m0/s1
SMILES Code
CC(OC[C@@H](C(C)=C)C/C=C(C)\C)=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
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 196.29 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.

Recalculate based on batch purity %
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: Govindarajan M, Benelli G. Eco-friendly larvicides from Indian plants: Effectiveness of lavandulyl acetate and bicyclogermacrene on malaria, dengue and Japanese encephalitis mosquito vectors. Ecotoxicol Environ Saf. 2016 Nov;133:395-402. doi: 10.1016/j.ecoenv.2016.07.035. Epub 2016 Aug 6. PubMed PMID: 27504617. 2: Cross H, Marriott R, Grogan G. Enzymatic esterification of lavandulol--a partial kinetic resolution of (S)-lavandulol and preparation of optically enriched (R)-lavandulyl acetate. Biotechnol Lett. 2004 Mar;26(5):457-60. PubMed PMID: 15104147. 3: Demissie ZA, Erland LA, Rheault MR, Mahmoud SS. The biosynthetic origin of irregular monoterpenes in Lavandula: isolation and biochemical characterization of a novel cis-prenyl diphosphate synthase gene, lavandulyl diphosphate synthase. J Biol Chem. 2013 Mar 1;288(9):6333-41. doi: 10.1074/jbc.M112.431171. Epub 2013 Jan 10. PubMed PMID: 23306202; PubMed Central PMCID: PMC3585068. 4: de Alfonso I, Hernandez E, Velazquez Y, Navarro I, Primo J. Identification of the sex pheromone of the mealybug Dysmicoccus grassii Leonardi. J Agric Food Chem. 2012 Dec 5;60(48):11959-64. doi: 10.1021/jf304065d. Epub 2012 Nov 20. PubMed PMID: 23167613. 5: Yadav KN, Adsul MG, Bastawde KB, Jadhav DD, Thulasiram HV, Gokhale DV. Differential induction, purification and characterization of cold active lipase from Yarrowia lipolytica NCIM 3639. Bioresour Technol. 2011 Nov;102(22):10663-70. doi: 10.1016/j.biortech.2011.09.013. Epub 2011 Sep 10. PubMed PMID: 21967715. 6: Hamilton JG, Hall DR, Kirk WD. Identification of a male-produced aggregation pheromone in the western flower thrips Frankliniella occidentalis. J Chem Ecol. 2005 Jun;31(6):1369-79. PubMed PMID: 16222777. 7: Fakhari AR, Salehi P, Heydari R, Ebrahimi SN, Haddad PR. Hydrodistillation-headspace solvent microextraction, a new method for analysis of the essential oil components of Lavandula angustifolia Mill. J Chromatogr A. 2005 Dec 9;1098(1-2):14-8. Epub 2005 Sep 6. PubMed PMID: 16314156. 8: Nasr M, Asgarpanah J. Volatile constituents of the seeds and fruit of Pycnocycla nodiflora. Nat Prod Commun. 2014 Dec;9(12):1781-2. PubMed PMID: 25632484. 9: Robu S, Aprotosoaie AC, Spac A, Cioancă O, Hăncianu M, Stănescu U. [Studies regarding chemical composition of lavender volatile oils]. Rev Med Chir Soc Med Nat Iasi. 2011 Apr-Jun;115(2):584-9. Romanian. PubMed PMID: 21870761. 10: Vaello T, Casas JL, Pineda A, de Alfonso I, Marcos-García MÁ. Olfactory Response of the Predatory Bug Orius laevigatus (Hemiptera:Anthocoridae) to the Aggregation Pheromone of Its Prey, Frankliniella occidentalis (Thysanoptera: Thripidae). Environ Entomol. 2017 Oct 1;46(5):1115-1119. doi: 10.1093/ee/nvx141. PubMed PMID: 28962006. 11: Li X, Geng S, Zhang Z, Zhang J, Li W, Huang J, Lin W, Bei Y, Lu Y. Species-specific aggregation pheromones contribute to coexistence in two closely related thrips species. Bull Entomol Res. 2018 May 21:1-8. doi: 10.1017/S0007485318000366. [Epub ahead of print] PubMed PMID: 29781420.