Eucamalol

CAS# 145544-91-8

Eucamalol

Catalog No. BCN1648----Order now to get a substantial discount!

Product Name & Size Price Stock
Eucamalol:5mg Please Inquire In Stock
Eucamalol:10mg Please Inquire In Stock
Eucamalol:20mg Please Inquire In Stock
Eucamalol:50mg Please Inquire In Stock

Quality Control of Eucamalol

Number of papers citing our products

Chemical structure

Eucamalol

3D structure

Chemical Properties of Eucamalol

Cas No. 145544-91-8 SDF Download SDF
PubChem ID 91884957 Appearance Oil
Formula C10H16O2 M.Wt 168.2
Type of Compound Monoterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3R,4R)-3-hydroxy-4-propan-2-ylcyclohexene-1-carbaldehyde
SMILES CC(C)C1CCC(=CC1O)C=O
Standard InChIKey ZPACRXLIAKZISA-ZJUUUORDSA-N
Standard InChI InChI=1S/C10H16O2/c1-7(2)9-4-3-8(6-11)5-10(9)12/h5-7,9-10,12H,3-4H2,1-2H3/t9-,10+/m1/s1
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.

Source of Eucamalol

The herbs of Eucalyptus camaldulensis

Biological Activity of Eucamalol

Description1. Eucamolol exhibits significant repellent activity against Aedes albopictus, and inhibits its feeding as well as DEET, is effective repellent (75%) up to 3 h after exposure to mosquito.

Eucamalol Dilution Calculator

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Eucamalol Molarity Calculator

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Preparing Stock Solutions of Eucamalol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.9453 mL 29.7265 mL 59.453 mL 118.9061 mL 148.6326 mL
5 mM 1.1891 mL 5.9453 mL 11.8906 mL 23.7812 mL 29.7265 mL
10 mM 0.5945 mL 2.9727 mL 5.9453 mL 11.8906 mL 14.8633 mL
50 mM 0.1189 mL 0.5945 mL 1.1891 mL 2.3781 mL 2.9727 mL
100 mM 0.0595 mL 0.2973 mL 0.5945 mL 1.1891 mL 1.4863 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.

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References on Eucamalol

Absolute configuration of a new mosquito repellent, (+)-eucamalol and the repellent activity of its epimer.[Pubmed:7613002]

Biosci Biotechnol Biochem. 1995 Jun;59(6):1139-41.

(+)-Eucamalol (1) and (-)-1-epi-Eucamalol (2) were synthesized from (S)-(-)-perillaldehyde to determine the absolute configuration of 1, the structure of natural (+)-Eucamalol being determined to be (1R,6R)-(+)-3-formyl-6-isopropyl-2-cyclohexen-1-ol. (+)-Eucamolol (1) and its 1-epimer (2) exhibited significant repellent activity against Aedes albopictus, and inhibited its feeding as well as DEET.

Polyoxygenated eudesmanes and trans-chrysanthemanes from the aerial parts of Santolina insularis.[Pubmed:14738382]

J Nat Prod. 2004 Jan;67(1):37-41.

The eudesmane sesquiterpenoids 1-3 and the trans-chrysanthemyl monoterpenoid 4 have been isolated from the aerial parts of Santolina insularis, a bush endemic to Sardinia. The absolute stereostructures of these novel compounds and of two known but incompletely characterized chrysanthemanes (5, 6) were established by spectroscopic techniques and by application of the modified Mosher method. The presence of the p-menthane aldehyde Eucamalol (7) gives credit to the widespread use of S. insularis to fend off mosquitoes.

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