13058-12-3

Basic information

• Product Name: ETHYL GERANATE
• Synonyms: ETHYL GERANATE;RARECHEM AL BI 0142;ethyl 3,7-dimethylocta-2,6-dienoate;2,6-Octadienoic acid, 3,7-dimethyl-, ethyl ester;ETHYL3,7-DIMETHYL-2,6-OCTADIENOATE;2,6-Octadienoic acid, 3,7-dimethyl-, ethyl ester 6-octadienoic acid, 3,7-dimethyl- ethyl ester 2,6-Octadienoic acid,3,7-dimethyl-,ethyl ester;3,7-Dimethyl-2,6-octadienoic acid ethyl ester;Ai3-25079
• CAS NO: 13058-12-3
• Molecular Formula: C₁₂H₂₀O₂
• Molecular Weight: 196.29
• EINECS: 235-948-6
• Mol File: 13058-12-3.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 266.1°Cat760mmHg
• Flash Point: 119.8°C
• Appearance: /
• Density: 0.904g/cm³
• Vapor Pressure: 0.00881mmHg at 25°C
• Refractive Index: 1.458
• CAS DataBase Reference: ETHYL GERANATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL GERANATE(13058-12-3)
• EPA Substance Registry System: ETHYL GERANATE(13058-12-3)

Safety Data

• Hazardous Substances Data: 13058-12-3(Hazardous Substances Data)

Usage

General Description

Ethyl geranate is a chemical compound that is commonly used in the fragrance and flavor industry. It is a clear, colorless liquid with a fruity, sweet, and floral aroma. Ethyl geranate is found naturally in various fruits, including raspberries, peaches, and oranges. It is often used as a scent component in perfumes, soaps, and personal care products. In addition to its use in the fragrance industry, ethyl geranate is also utilized as a flavor enhancer in food and beverages, adding a fruity, sweet taste to products such as candy, chewing gum, and beverages. It is generally recognized as safe for use in food by the US Food and Drug Administration.

InChI:InChI=1/C12H20O2/c1-5-14-12(13)9-11(4)8-6-7-10(2)3/h7,9H,5-6,8H2,1-4H3

Upstream product

• 51318-62-8 ethyl 4-bromo-3-methylcrotonate 
• 870-63-3 prenyl bromide 
• 64-17-5 ethanol 
• 858251-08-8 3,7-dimethyloct-2,6-dienylacyl chloride 
• 91232-81-4 ((E)-1-Ethoxy-3-methyl-buta-1,3-dienyloxy)-trimethyl-silane 
• 503-60-6 3,3-dimethyl-allyl chloride 
• 92511-62-1 ethyl 3-methyl-4-(tributylstannyl)-2-butenoate 
• 79858-00-7 α-sulfinyl citronellate 
• 112157-80-9 (E)-3,7-Dimethyl-6-phenylsulfanyl-octa-2,7-dienoic acid ethyl ester 
• 996-82-7 sodium diethylmalonate 
• 110-93-0 6-Methyl-hept-5-en-2-on 
• 4071-88-9 trimethylsilanyl-acetic acid ethyl ester 
• 20608-08-6 diethyl phosphonoacetic acid 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 

Downstream Products

• 459-80-3 geranic acid 
• 106-25-2 Nerol 
• 5944-27-4 ethyl 3,7-dimethyloctanoate 
• 624-15-7 geraniol 
• 106-24-1 Geraniol 
• 105-90-8 geranyl propionate 
• 105-87-3 3,7-dimethyl-2E,6-octadien-1-yl acetate 
• 109-20-6 [(2E)-3,7-dimethylocta-2,6-dienyl] 3-methylbutanoate 
• 5392-40-5 (E/Z)-3,7-dimethyl-2,6-octadienal 
• 142747-09-9 2-(1-hydroxymethyl-2,6,6-trimethyl-2-cyclohexenyl)ethanol 
• 142747-10-2 3-(1-hydroxymethyl-2,6,6-trimethyl-2-cyclohexenyl)propanol 
• 142747-06-6 ethyl (1-ethoxycarbonyl-2,6,6-trimethyl-2-cyclohexenyl)acetate 
• 142747-07-7 ethyl 3-(1-ethoxycarbonyl-2,6,6-trimethyl-2-cyclohexenyl)propionate 
• 6138-90-5 trans-geranyl bromide 

Relevant articles and documents

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INSECT PHEROMONES AND THEIR ANALOGUES XXX. SYNTHESIS OF OCTA-2E,6E-DIENE-1,8-DIOL DIISOVALERATE - THE SEX PHEROMONE OF Agriotes tauricus

The synthesis has been effected of octa-2E,6E-diene-1,8-diol diisovalerate - the sex pheromone of the Crimean click beetle Agriotes tauricus - by the carboxymethylenation of the readilly available 6-methylhept-5-en-2-one, the allyl oxidation of a terminal methyl group, reduction of the ester fraction, and interaction of the diol so obtained with isovaleryl chloride.The required pheromone can also bee obtained from available cyclic oligomers of isoprene.

Transition-Metal-Free Formylation of Allylzinc Reagents Leading to α-Quaternary Aldehydes

The first example of formylation of allylzinc reagents using S-phenyl thioformate is presented. The reaction proceeded under mild conditions without any transition-metal catalyst, forming quaternary carbon centers with reactive functionalities, such as formyl and vinyl groups. Moreover, Barbier-type formylation of an allylic bromide with a sterically demanding thioformate was achieved. As a preliminary result, asymmetric formylation was conducted using a menthol-derived chiral thioformate.

Agent having neurotrophic factor-like activity

The present invention provides a pharmaceutical agent having high safety and a neurotrophic factor-like activity, which contains, as an active ingredient, any one compound included in fatty acids each having 8 carbon atoms (C8) or having 10 carbon atoms (C10) to 12 carbon atoms (C12) or fatty acid esters thereof, such as 3,7-dimethyloctanoic acid ethyl ester, geranicacidethyl ester, and the like, eachof whichhas 8 carbonatoms (C8), decanoic acid methyl ester, trans-2-decenoic acid, trans-2-decenoic acid methyl ester, trans-2-decenoic acid ethyl ester, trans-2-decenoic acid-2-decenyl ester, trans-2-decenoic acid cyclohexyl ester, trans-2-decenoic acid isopropyl ester, trans-3-decenoic acid methyl ester, trans-9-decenoic acid methyl ester, and the like, each of which has 10 carbon atoms (C10), trans-10-undecenoic acid methyl ester, trans-10-undecenoic acid ethyl ester, and the like, each of which has 11 carbon atoms (C11), and dodecanoic acid, and the like, each of which has 12 carbon atoms (C12), or salts thereof or prodrugs thereof.