Ethyl (2E,4Z)-deca-2,4-dienoateCAS# 3025-30-7 |
2D Structure
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
Cas No. | 3025-30-7 | SDF | Download SDF |
PubChem ID | 5281162.0 | Appearance | Powder |
Formula | C12H20O2 | M.Wt | 196.29 |
Type of Compound | Aliphatics | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | ethyl (2E,4Z)-deca-2,4-dienoate | ||
SMILES | CCCCCC=CC=CC(=O)OCC | ||
Standard InChIKey | OPCRGEVPIBLWAY-QNRZBPGKSA-N | ||
Standard InChI | InChI=1S/C12H20O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h8-11H,3-7H2,1-2H3/b9-8-,11-10+ | ||
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
||
About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
||
Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. |
Ethyl (2E,4Z)-deca-2,4-dienoate Dilution Calculator
Ethyl (2E,4Z)-deca-2,4-dienoate Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 5.0945 mL | 25.4725 mL | 50.945 mL | 101.8901 mL | 127.3626 mL |
5 mM | 1.0189 mL | 5.0945 mL | 10.189 mL | 20.378 mL | 25.4725 mL |
10 mM | 0.5095 mL | 2.5473 mL | 5.0945 mL | 10.189 mL | 12.7363 mL |
50 mM | 0.1019 mL | 0.5095 mL | 1.0189 mL | 2.0378 mL | 2.5473 mL |
100 mM | 0.0509 mL | 0.2547 mL | 0.5095 mL | 1.0189 mL | 1.2736 mL |
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. |
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- Morroniaglycone
Catalog No.:BCX1365
CAS No.:1644061-02-8
- Crocetindial
Catalog No.:BCX1364
CAS No.:502-70-5
- Gymnoside VII
Catalog No.:BCX1363
CAS No.:899430-07-0
- Blestriarene B
Catalog No.:BCX1362
CAS No.:127211-03-4
- 6-Benzoylheteratisine
Catalog No.:BCX1361
CAS No.:99759-48-5
- Ilexoside O
Catalog No.:BCX1360
CAS No.:136552-23-3
- Neokurarinol
Catalog No.:BCX1359
CAS No.:52483-00-8
- Cantleyoside
Catalog No.:BCX1358
CAS No.:32455-46-2
- 6""-apiosyl sec-O-glucosylhamaudol
Catalog No.:BCX1357
CAS No.:2254096-95-0
- (3R)-dihydroarteannuin B
Catalog No.:BCX1356
CAS No.:87206-33-5
- Eugenitin
Catalog No.:BCX1355
CAS No.:480-12-6
- Ajugamacrin B
Catalog No.:BCX1354
CAS No.:123313-59-7
- Myristoleic acid
Catalog No.:BCX1367
CAS No.:544-64-9
- Elaidic acid methyl ester
Catalog No.:BCX1368
CAS No.:1937-62-8
- Cis-11-Eicosenoic acid
Catalog No.:BCX1369
CAS No.:5561-99-9
- Octadec-11-enoic acid
Catalog No.:BCX1370
CAS No.:693-72-1
- Tridecanoic acid
Catalog No.:BCX1371
CAS No.:638-53-9
- Methyl tridecanoate
Catalog No.:BCX1372
CAS No.:1731-88-0
- Pentadecanoic acid
Catalog No.:BCX1373
CAS No.:1002-84-2
- Heptadecanoic acid
Catalog No.:BCX1374
CAS No.:506-12-7
- Methyl heptadecanoate
Catalog No.:BCX1375
CAS No.:1731-92-6
- Nonadecanoic acid
Catalog No.:BCX1376
CAS No.:646-30-0
- Ethyl palmitoleate
Catalog No.:BCX1377
CAS No.:56219-10-4
- Palmitoleic acid
Catalog No.:BCX1378
CAS No.:373-49-9
Molecular and Functional Characterization of Three General Odorant-Binding Protein 2 Genes in Cydia pomonella (Lepidoptera: Tortricidae).[Pubmed:38339028]
Int J Mol Sci. 2024 Feb 1;25(3):1746.
General odorant-binding proteins (GOBPs) play a crucial role in the detection of host plant volatiles and pheromones by lepidopterans. Previous studies identified two duplications in the GOBP2 gene in Cydia pomonella. In this study, we employed qRT-PCR, protein purification, and fluorescence competitive binding assays to investigate the functions of three GOBP2 genes in C. pomonella. Our findings reveal that CpomGOBP2a and CpomGOBP2b are specifically highly expressed in antennae, while CpomGOBP2c exhibits high specific expression in wings, suggesting a potential divergence in their functions. Recombinant proteins of CpomGOBP2a, CpomGOBP2b, and CpomGOBP2c were successfully expressed and purified, enabling an in-depth exploration of their functions. Competitive binding assays with 20 host plant volatiles and the sex pheromone (codlemone) demonstrated that CpomGOBP2a exhibits strong binding to four compounds, namely butyl octanoate, Ethyl (2E,4Z)-deca-2,4-dienoate (pear ester), codlemone, and geranylacetone, with corresponding dissolution constants (Ki) of 8.59993 muM, 9.14704 muM, 22.66298 muM, and 22.86923 muM, respectively. CpomGOBP2b showed specific binding to pear ester (Ki = 17.37481 muM), while CpomGOBP2c did not exhibit binding to any tested compounds. In conclusion, our results indicate a functional divergence among CpomGOBP2a, CpomGOBP2b, and CpomGOBP2c. These findings contribute valuable insights for the development of novel prevention and control technologies and enhance our understanding of the evolutionary mechanisms of olfactory genes in C. pomonella.
Yeast Volatomes Differentially Affect Larval Feeding in an Insect Herbivore.[Pubmed:31444202]
Appl Environ Microbiol. 2019 Oct 16;85(21):e01761-19.
Yeasts form mutualistic interactions with insects. Hallmarks of this interaction include provision of essential nutrients, while insects facilitate yeast dispersal and growth on plant substrates. A phylogenetically ancient chemical dialogue coordinates this interaction, where the vocabulary, the volatile chemicals that mediate the insect response, remains largely unknown. Here, we used gas chromatography-mass spectrometry, followed by hierarchical cluster and orthogonal partial least-squares discriminant analyses, to profile the volatomes of six Metschnikowia spp., Cryptococcus nemorosus, and brewer's yeast (Saccharomyces cerevisiae). The yeasts, which are all found in association with insects feeding on foliage or fruit, emit characteristic, species-specific volatile blends that reflect the phylogenetic context. Species specificity of these volatome profiles aligned with differential feeding of cotton leafworm (Spodoptera littoralis) larvae on these yeasts. Bioactivity correlates with yeast ecology; phylloplane species elicited a stronger response than fruit yeasts, and larval discrimination may provide a mechanism for establishment of insect-yeast associations. The yeast volatomes contained a suite of insect attractants known from plant and especially floral headspace, including (Z)-hexenyl acetate, Ethyl (2E,4Z)-deca-2,4-dienoate (pear ester), (3E)-4,8-dimethylnona-1,3,7-triene (DMNT), linalool, alpha-terpineol, beta-myrcene, or (E,E)-alpha-farnesene. A wide overlap of yeast and plant volatiles, notably floral scents, further emphasizes the prominent role of yeasts in plant-microbe-insect relationships, including pollination. The knowledge of insect-yeast interactions can be readily brought to practical application, as live yeasts or yeast metabolites mediating insect attraction provide an ample toolbox for the development of sustainable insect management.IMPORTANCE Yeasts interface insect herbivores with their food plants. Communication depends on volatile metabolites, and decoding this chemical dialogue is key to understanding the ecology of insect-yeast interactions. This study explores the volatomes of eight yeast species which have been isolated from foliage, from flowers or fruit, and from plant-feeding insects. These yeasts each release a rich bouquet of volatile metabolites, including a suite of known insect attractants from plant and floral scent. This overlap underlines the phylogenetic dimension of insect-yeast associations, which according to the fossil record long predate the appearance of flowering plants. Volatome composition is characteristic for each species, aligns with yeast taxonomy, and is further reflected by a differential behavioral response of cotton leafworm larvae, which naturally feed on foliage of a wide spectrum of broad-leaved plants. Larval discrimination may establish and maintain associations with yeasts and is also a substrate for designing sustainable insect management techniques.