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127 results about "Methyl dihydrojasmonate" patented technology

Methyl dihydrojasmonate is an aroma compound, that smells similar to jasmine. In racemic mixtures the odor is floral and citrus while epimerized mixtures exhibit a dense fatty floral odor with odor recognition thresholds of 15 parts per billion.

Fragrance compositions

A method of promoting activated, pleasant moods through the inhalation of energising, non-stressing fragrances (invigorating fragrances) comprising at least 75% by weight, preferably 85% by weight of perfume materials drawn from the following groups:
  • A) At least 10% by weight in total of at least three materials drawn from Group ‘IMP’ comprising: allyl amyl glycolate; benzyl salicylate; bergamot oil; coriander oil; cyclamen aldehyde; 1-(2,6,10-trimethylcyclododeca-2,5,9-trien-1-yl)ethanone; allyl (cyclohexyloxy)acetate; Damascenia 185 SAE; 2,4-dimethylheptan-1-ol; fir balsam; fir needle oil; 3-(4-ethylphenyl)-2,2-dimethylpropanal; ginger oil; guaiacwood; linalyl acetate; litsea cubeba oil; methyl 2,4-dihydroxy-3,6-dimethylbenzoate; nutmeg oil; olibanum oil; orange flower oil; Ozonal AB 7203C; patchouli oil; rose oxide; rosemary oil; sage clary oil; spearmint oil; Tamarine AB 8212E; tarragon oil;
  • B) Optionally up to 90% of materials from the following groups:
    • Group ‘HMR’ comprising:
    • allyl ionone; benzyl acetate; cis-jasmone; citronellol; ethyl linalol; ethylene brassylate; 4-methyl-2-(2-methylpropyl)tetrahydro-2H-pyran-4-ol; geraniol; geranium oil; isoeugenol; lemon oil; 2,4-dimethylcyclohex-3-ene-1-carbaldehyde; 3-(4-hydroxy-4-methylpentyl)cyclohex-3-ene-1-carbaldehyde; 4-(4-hydroxy-4-methylpentyl)cyclohex-3-ene-1-carbaldehyde; alpha-iso-methyl ionone; 3-methylcyclopentadec-2-en-1-one; cyclopentadecanone; cyclohexadecanolide; gamma-undecalactone.
    • Group ‘HMI’ comprising:
    • 1-{[2-(1,1 -dimethylethyl)cyclohexyl]oxy}butan-2-ol; 3a,6,6,9a-tetramethyldodecahydronaphtho[2,1 -{b}]furan; alpha-damascone; dihydromyrcenol; eugenol; 3-(1,3-benzodioxol-5-yl)-2-methylpropanal; 2,4-dimethylcyclohex-3-ene-1-carbaldehyde; mandarin oil; orange oil; 2-(1,1-dimethylethyl)cyclohexyl acetate.
    • Group ‘HMP’ comprising:
    • 1-(2,6,6,8-tetramethyltricyclo[5.3.1.0 {1,5}]undec-8-en-9-yl)ethanone; allyl cyclohexyl propionate; allyl heptanoate; Apple Oliffac S pcmf; 7-methyl-2H-1,5-benzodioxepin-3(4H)-one; cassis base; cis-3-hexenyl salicylate; damascenone; gamma-decalactone; ethyl acetoacetate; ethyl maltol; ethyl methyl phenylglycidate; hexyl acetate; (3E)-4-methyldec-3-en-5-ol; 2,5,5-trimethyl-6,6-bis(methyloxy)hex-2-ene; 4-(4-hydroxyphenyl)butan-2-one; styrallyl acetate; 2,2,5-trimethyl-5-pentylcyclopentanone; ylang oil. Group ‘RMP’ comprising: anisic aldehyde; (2Z)-2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol; benzoin siam resinoid; ethyl vanillin; oxacyclohexadec-12(13)-en-2-one; hexyl salicylate; hydroxycitronellal; jasmin oil; 3-methyl-5-phenylpentan-1-ol; 2-(phenyloxy)ethyl 2-methylpropanoate; alpha-terpineol; vanillin;
    • Group ‘GEN’ comprising:
    • cyclopentadecanolide; oxacyclohexadecan-2-one; hexyl cinnamic aldehyde; ionone beta; isobornyl cyclohexanol; 1-(2,3,8,8-tetramethyl-1,2,3,4,5,6,7(8),8(8a)-octahydronaphthalen-2-yl)ethanone; 4-(1,1-dimethylethyl)phenyl]-2-methylpropanal; linalol; methyl dihydrojasmonate; 2-phenylethanol;
    • provided the following conditions are met:
    • (a) IMPs>=HMPs+HMRs
    • (b) IMPs+HMIs+GENs>=70%
    • (c) (IMP+HMI)/(IMP+HMI+RMP+HMR)>=0.7
    • (d) IMPs/(HMPs+RMPs+IMPs)>=0.5
    • (e) IMPs/[(HMPs+RMPs+IMPs)+(100−TOTAL)]>=0.3
    • wherein ‘IMPs’ indicates the sum of the percentages of materials within Group IMP, and similarly for the remaining groups, the symbol ‘>=’ indicates ‘at least equal to’, and ‘TOTAL’ is the sum of HMPs, HMRs, HMIs, IMPs, RMPs and GENs, provided also that low odour or no odour solvents are excluded from the calculation of these sums is provided which have an invigorating effect when inhaled by a subject.
Owner:GIVAUDAN NEDERLAND SERVICES

Method for producing 2-alkylidene cyclopentanone

The invention discloses an environment-friendly method for producing 2-alkylidene cyclopentanone, which uses cyclopentanone and fatty aldehyde as raw materials and uses amine type weak-base ion-exchange resin for reaction under the condition of existence of fatty acid to produce 2-alkylidene cyclopentanone. The resin and the fatty acid which are separated can be recycled. The 2-alkylidene cyclopentanone is a key intermediate for synthesizing many spices (such as methyl dihydrojasmonate and delta-lactone). The traditional technology of the 2-alkylidene cyclopentanone has the outstanding problems that the acid-base solution catalytic system is adopted, which causes that the catalyst is very difficult to be recycled, the product yield is low, many by-products with high boiling points are generated, the reaction selectivity is poor, and a large amount of waste water is generated, thereby wasting resources and polluting environment. The method of the invention uses a catalytic system whichcan be recycled to replace the traditional solution catalytic system which can not be recycled, uses the cleaning production technology to improve the original technology, and simultaneously achievesthe purposes of saving and fully utilizing resources and protecting the environment.
Owner:河南蔚源生物科技有限公司
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