9-Decenyl acetate

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

MedKoo CAT#: 582031

CAS#: 50816-18-7

Description: 9-Decenyl acetate is a biochemical.


Chemical Structure

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9-Decenyl acetate
CAS# 50816-18-7

Theoretical Analysis

MedKoo Cat#: 582031
Name: 9-Decenyl acetate
CAS#: 50816-18-7
Chemical Formula: C12H22O2
Exact Mass: 198.16
Molecular Weight: 198.310
Elemental Analysis: C, 72.68; H, 11.18; O, 16.14

Price and Availability

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). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: 9-Decenyl acetate; 9-Decen-1-ol, acetate; AI3-34397; BRN 1765355; Decenyl acetate; EINECS 256-784-1; UNII-I999R8F793.

IUPAC/Chemical Name: dec-9-en-1-yl acetate

InChi Key: PIQXMYAEJSMANF-UHFFFAOYSA-N

InChi Code: InChI=1S/C12H22O2/c1-3-4-5-6-7-8-9-10-11-14-12(2)13/h3H,1,4-11H2,2H3

SMILES Code: C(CCCCCCC=C)COC(C)=O

Appearance: Liquid

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

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 198.31 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
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Grodner J, Świech K, Jakubowska M, Bocianowski J. Attraction of Moths of Two Noctuidae Species to Field Traps Baited With a Mixture of two to three Homologous Acetates in Poland. J Econ Entomol. 2018 Aug 3;111(4):1664-1673. doi: 10.1093/jee/toy096. PubMed PMID: 29697826.

2: Ding BJ, Löfstedt C. Analysis of the Agrotis segetum pheromone gland transcriptome in the light of sex pheromone biosynthesis. BMC Genomics. 2015 Sep 18;16:711. doi: 10.1186/s12864-015-1909-2. PubMed PMID: 26385554; PubMed Central PMCID: PMC4575462.

3: Zhang DD, Löfstedt C. Functional evolution of a multigene family: orthologous and paralogous pheromone receptor genes in the turnip moth, Agrotis segetum. PLoS One. 2013 Oct 10;8(10):e77345. doi: 10.1371/journal.pone.0077345. eCollection 2013. PubMed PMID: 24130875; PubMed Central PMCID: PMC3795068.

4: Alagarmalai J, Nestel D, Dragushich D, Nemny-Lavy E, Anshelevich L, Zada A, Soroker V. Identification of host attractants for the ethiopian fruit fly, Dacus ciliatus loew. J Chem Ecol. 2009 May;35(5):542-51. doi: 10.1007/s10886-009-9636-2. Epub 2009 May 14. PubMed PMID: 19440796.

5: Schlamp KK, Gries R, Khaskin G, Brown K, Khaskin E, Judd GJ, Gries G. Pheromone components from body scales of female Anarsia lineatella induce contacts by conspecific males. J Chem Ecol. 2005 Dec;31(12):2897-911. Epub 2005 Dec 18. PubMed PMID: 16365712.

6: Inomata S, Watanabe A, Nomura M, Ando T. Mating communication systems of four Plusiinae species distributed in Japan: identification of the sex pheromones and field evaluation. J Chem Ecol. 2005 Jun;31(6):1429-42. PubMed PMID: 16222781.

7: Pophof B, Gebauer T, Ziegelberger G. Decyl-thio-trifluoropropanone, a competitive inhibitor of moth pheromone receptors. J Comp Physiol A. 2000 Mar;186(3):315-23. PubMed PMID: 10757247.

8: Gustavsson AL, Larsson MC, Hansson BS, Liljefors T. Enantiomers of cis- and trans-3-(4-propyl-cyclopent-2-enyl) propyl acetate. A study on the bioactive conformation and chiral recognition of a moth sex pheromone component. Bioorg Med Chem. 1997 Dec;5(12):2173-83. PubMed PMID: 9459015.

9: Jönsson S, Hansson BS, Liljefors T. Conformationally constrained analogues of (Z)-5-decenyl acetate, a pheromone component of Agrotis segetum. Bioorg Med Chem. 1996 Mar;4(3):499-504. PubMed PMID: 8733633.

10: Bestmann HJ, Roth KD, Rehefeld C, Leinemann B, Kern F, Vostrowsky O. Ab initio calculations on (Z)-5-decenyl acetate, a component of the pheromone complex of Agrotis segetum (Lepidoptera: Noctuidae) and electrophysiological studies with chain elongated analogues. Bioorg Med Chem. 1996 Mar;4(3):473-7. PubMed PMID: 8733629.

11: Gustavsson AL, Liljefors T, Hansson BS. Alkyl ether and enol ether analogs of (Z)-5-decenyl acetate, a pheromone component of the turnip moth,Agrotis segetum: probing a proposed bioactive conformation for chain-elongated analogs. J Chem Ecol. 1995 Jun;21(6):815-32. doi: 10.1007/BF02033463. PubMed PMID: 24234320.

12: Löfstedt C, Hansson BS, Tòth M, Szöcs G, Buda V, Bengtsson M, Ryrholm N, Svensson M, Priesner E. Pheromone differences between sibling taxaDiachrysia chrysitis (linnaeus, 1758) andD. tutti (Kostrowicki, 1961) (Lepidoptera: Noctuidae). J Chem Ecol. 1994 Jan;20(1):91-109. doi: 10.1007/BF02065993. PubMed PMID: 24241701.

13: Jönsson S, Malmström T, Liljefors T, Hansson BS. Enantiomers of methyl substituted analogs of (Z)-5-decenyl acetate as probes for the chirality and complementarity of its receptor inAgrotis segetum 1: Synthesis and structure-activity relationships. J Chem Ecol. 1993 Mar;19(3):459-84. doi: 10.1007/BF00994319. PubMed PMID: 24248950.

14: Wenqi W, Bengtsson M, Hansson BS, Liljefors T, Löfstedt C, Prestwich GD, Sun WC, Svensson M. Electrophysiological and behavioral responses of turnip moth males,Agrotis segetum to fluorinated pheromone analogs. J Chem Ecol. 1993 Jan;19(1):143-57. doi: 10.1007/BF00987479. PubMed PMID: 24248519.

15: Tòth M, Löfstedt C, Blair BW, Cabello T, Farag AI, Hansson BS, Kovalev BG, Maini S, Nesterov EA, Pajor I, Sazonov AP, Shamshev IV, Subchev M, Szöcs G. Attraction of male turnip mothsAgrotis segetum (Lepidoptera: Noctuidae) to sex pheromone components and their mixtures at 11 sites in Europe, Asia, and Africa. J Chem Ecol. 1992 Aug;18(8):1337-47. doi: 10.1007/BF00994360. PubMed PMID: 24254210.

16: Jönsson S, Liljefors T, Hansson BS. Introduction of methyl groups to acetate substituted chain of (Z)-5-decenyl acetate, a pheromone component of turnip moth,agrotis segetum: synthesis, single-sensillum recordings, and structure-activity relationships. J Chem Ecol. 1992 Apr;18(4):637-57. doi: 10.1007/BF00987825. PubMed PMID: 24253872.

17: Jönsson S, Liljefors T, Hansson BS. Replacement of the terminal methyl group in a moth sex pheromone component by a halogen atom: Hydrophobicity and size effects on electrophysiological single-cell activities. J Chem Ecol. 1991 Jul;17(7):1381-97. doi: 10.1007/BF00983771. PubMed PMID: 24257799.

18: Witzgall P, Priesner E. Wind-tunnel study on attraction inhibitor in maleColeophora laricella Hbn. (Lepidoptera: Coleophoridae). J Chem Ecol. 1991 Jul;17(7):1355-62. doi: 10.1007/BF00983768. PubMed PMID: 24257796.

19: Jönsson S, Liljefors T, Hansson BS. Alkyl substitution in terminal chain of (Z)-5-decenyl acetate, a pheromone component of turnip moth,Agrotis segetum. Synthesis, single-sensillum recordings, and structure-activity relationships. J Chem Ecol. 1991 Jan;17(1):103-22. doi: 10.1007/BF00994425. PubMed PMID: 24258437.

20: Hansson BS, Tóth M, Löfstedt C, Szöcs G, Subchev M, Löfqvist J. Pheromone variation among eastern European and a western Asian population of the turnip mothAgrotis segetum. J Chem Ecol. 1990 May;16(5):1611-22. doi: 10.1007/BF01014094. PubMed PMID: 24263831.