Geranylacetate

CAS# 105-87-3

Geranylacetate

Catalog No. BCN9992----Order now to get a substantial discount!

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Quality Control of Geranylacetate

Number of papers citing our products

Chemical structure

Geranylacetate

3D structure

Chemical Properties of Geranylacetate

Cas No. 105-87-3 SDF Download SDF
PubChem ID 1549026 Appearance Oil
Formula C12H20O2 M.Wt 196.3
Type of Compound Monoterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(2E)-3,7-dimethylocta-2,6-dienyl] acetate
SMILES CC(=CCCC(=CCOC(=O)C)C)C
Standard InChIKey HIGQPQRQIQDZMP-DHZHZOJOSA-N
Standard InChI InChI=1S/C12H20O2/c1-10(2)6-5-7-11(3)8-9-14-12(4)13/h6,8H,5,7,9H2,1-4H3/b11-8+
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 Geranylacetate

The volatile oil of the fruit from phellodendron Amurense Rupr.

Biological Activity of Geranylacetate

DescriptionGeranyl acetate is widely used in the fragrance and cosmetic industries, and thus has great economic value.

Geranylacetate Dilution Calculator

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Geranylacetate Molarity Calculator

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Preparing Stock Solutions of Geranylacetate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.0942 mL 25.4712 mL 50.9424 mL 101.8849 mL 127.3561 mL
5 mM 1.0188 mL 5.0942 mL 10.1885 mL 20.377 mL 25.4712 mL
10 mM 0.5094 mL 2.5471 mL 5.0942 mL 10.1885 mL 12.7356 mL
50 mM 0.1019 mL 0.5094 mL 1.0188 mL 2.0377 mL 2.5471 mL
100 mM 0.0509 mL 0.2547 mL 0.5094 mL 1.0188 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.

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References on Geranylacetate

Chemical constituent and antimicrobial effect of essential oil from Myrtus communis leaves on microorganisms involved in persistent endodontic infection compared to two common endodontic irrigants: An in vitro study.[Pubmed:25298646]

J Conserv Dent. 2014 Sep;17(5):449-53.

INTRODUCTION: Persistent infections of human root canals play a fundamental role in the failure of endodontic treatment. The purpose of this study is to determine the chemical composition of Myrtus communis (M. communis) essential oil and to assess its antimicrobial activity against Enterococcus faecalis, Staphylococcus aureus and Candida albicans compared to that of sodium hypochlorite (NaOCl) and chlorhexidine (CHX). MATERIALS AND METHODS: Gas chromatography-mass spectrometry (GC-MS) was used to determine the chemical composition of essential oil from M. communis leaves. A micro-dilution susceptibility assay and disk diffusion methods were utilized to evaluate the antimicrobial activity [minimum inhibitory concentration (MIC) and minimum lethal dose concentration] of the tested solutions against selected microorganisms. RESULTS: GC-MS analyses revealed that M. communis contained 1, 8-Cineole (28.62%), alpha-Pinene (17.8%), Linalool (17.55%), and Geranylacetate (6.3%) as the major compounds and Geraniol (1.6%), alpha-Humulene (1.5%), eugenol (1.3%), isobutyl-isobutyrate (0.8%), and methyl chavicol (0.5%) as minor components. Chlorhexidine had the lowest MIC value among all medicaments tested. M. communis oil had less MIC values than NaOCl against both bacteria, but it had more MIC value against C. albicans. CONCLUSION: M. communis essential oil with the minimum inhibitory concentration in the range of 0.032-32 mug/mL was an effective antimicrobial agent against persistent endodontic microorganisms.

Efficient and selective microbial esterification with dry mycelium of Rhizopus oryzae.[Pubmed:11604169]

J Biotechnol. 2001 Dec 14;92(1):21-6.

The use of dry mycelium of Rhizopus oryzae as biocatalyst for ester production in organic solvent has been studied. Mycelia with notable carboxylesterase activity were produced when different Tweens (20, 40, 60 and 80) were employed as main carbon source for the growth. Dry mycelium of four strains of Rhizopus oryzae proved effective for efficiently catalysing the synthesis of different flavour esters (hexylacetate and butyrate, Geranylacetate and butyrate) starting from the corresponding alcohol and free acid, including acetic acid. The esterification of the racemic mixture of 2-octanol and butyric acid proceeded with high enantioselectivity (R-ester produced with enantiomeric excess > or =97%) when Rhizopus oryzae CBS 112.07 and Rhizopus oryzae CBS 260.28 were employed.

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