Jasmone

Jasmone Basic information
Product Name:Jasmone
Synonyms:CIS-3-METHYL-2-(2-PENTENYL)-2-CYCLOPENTEN-1-ONE;FEMA 3196;JASMONE;JASMONE, CIS-;3-METHYL-2-(CIS-2-PENTENYL)-2-CYCLOPENTEN-1-ONE;3-METHYL-2-(2-PENTENYL)-2-CYCLOPENTEN-1-ONE;(z)-2-cyclopenten-1-on;2-Cyclopenten-1-one,3-methyl-2-(2-pentenyl)-,(Z)-
CAS:488-10-8
MF:C11H16O
MW:164.24
EINECS:207-668-4
Product Categories:ketone Flavor
Mol File:488-10-8.mol
Jasmone Structure
Jasmone Chemical Properties
Boiling point 134-135 °C12 mm Hg(lit.)
density 0.94 g/mL at 25 °C(lit.)
vapor pressure 0.91Pa at 20℃
refractive index n20/D 1.498(lit.)
FEMA 3196 | 3-METHYL-2-(2-PENTENYL)-2-CYCLOPENTEN-1-ONE
Fp 225 °F
storage temp. Sealed in dry,Room Temperature
form neat
color Colorless to Light orange to Yellow
Odorat 10.00 % in dipropylene glycol. woody herbal floral spicy jasmin celery
Odor Typefloral
Water Solubility 1.48g/L at 20℃
JECFA Number1114
Merck 14,5259
BRN 1907713
InChIKeyIVLCENBZDYVJPA-ARJAWSKDSA-N
LogP2.8 at 35℃
CAS DataBase Reference488-10-8(CAS DataBase Reference)
NIST Chemistry Reference2-Cyclopenten-1-one, 3-methyl-2-(2-pentenyl)-, (Z)-(488-10-8)
EPA Substance Registry System2-Cyclopenten-1-one, 3-methyl-2-(2Z)-2-pentenyl- (488-10-8)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 2
RTECS GY7301000
TSCA Yes
HS Code 29142990
Hazardous Substances Data488-10-8(Hazardous Substances Data)
Toxicityrabbit,LD50,skin,> 5gm/kg (5000mg/kg),Food and Cosmetics Toxicology. Vol. 17, Pg. 845, 1979.
MSDS Information
ProviderLanguage
Jasmone English
SigmaAldrich English
ALFA English
Jasmone Usage And Synthesis
DescriptionThis has a jasmine odor.
Chemical PropertiesColorless viscous liquid
Chemical PropertiesJasmone has a floral, fruity, jasmine odor. cis-Jasmone is widely used in the creation of high quality florals like jasmine and tuberose. Also used in the reconstitution of synthetic essential oils.
OccurrenceThe cis-form is reportedly occurring naturally; it is found in the essential oils of jasmine (3%), jonquil, and Pittosporum glabratum, in neroli oil, in peppermint (Mentha piperita), and in bergamot, apricot, raspberry, cinnamon, corn mint and spearmint oils, beer, tea, soybean and heated beans.
UsesPerfumery.
DefinitionA ketone found in jasmine oil and other flower oils.
Taste threshold valuesTaste characteristics at 25 ppm: woody, bitter, tea, with a citrus and floral nuance.
Synthesis Reference(s)The Journal of Organic Chemistry, 39, p. 2317, 1974 DOI: 10.1021/jo00929a053
Synthetic Communications, 5, p. 1, 1975 DOI: 10.1080/00397917508063507
Flammability and ExplosibilityNotclassified
SynthesisA review and classification on the synthesis of jasmone is available.
ISO-JASMONE PURE Jasmone Methyl 9-OXO-15S-HYDROXY-PROSTA-5Z,8(12),13E,17Z-TETRAEN-1-OIC ACID 10 G METHYL JASMONATEPURE 19(R)-HYDROXY PROSTAGLANDIN B2 METHYL JASMONATE PROSTAGLANDIN B2 LACTONE OF CIS JASMONE DI JASMONE,Jasmone, dihydro- TRANS-JASMONE CIS-JASMONE = 3-METHYL-2-(2-CIS-PENTEN-1-YL)-2-CYCLOPENTEN-1-ON = JASMONE 9-OXO-15S-HYDROXY-PROSTA-5Z,8(12),13E-TRIEN-1-OIC-3,3,4,4-D4 ACID JASMINE Cyclethrin JASMONE, cis-(SG),DI JASMONE Methyl dihydrojasmonate METHYL THIOPHENE-2-CARBOXYLATE

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