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2-Pentyl-3-methyl-2-cyclopenten-1-one

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Products Intro: Product Name:2-Pentyl-3-methyl-2-cyclopenten-1-one
CAS:1128-08-1
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CAS:1128-08-1
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Products Intro: Product Name:DIHYDRO JASMONE
CAS:1128-08-1
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CAS:1128-08-1
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Products Intro: Product Name: 2-Pentyl-3-methyl-2-cyclopenten-1-one
CAS:1128-08-1
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2-Pentyl-3-methyl-2-cyclopenten-1-one manufacturers

  • Dihydrojasmone
  • Dihydrojasmone pictures
  • $29.00 / 1g
  • 2026-05-11
  • CAS:1128-08-1
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  • Purity: 99.75%
  • Supply Ability: 10g
2-Pentyl-3-methyl-2-cyclopenten-1-one Basic information
Aroma Uses in Perfume
Product Name:2-Pentyl-3-methyl-2-cyclopenten-1-one
Synonyms:3-METHYL-2-PENTYL-2-CYCLOPENTEN-1-ONE;3-METHYL-2-PENTYL-2-CYCLOPENTENONE;DihydrojasMone (mixture of isomers);3-Methyl-2-(n-pentanyl)-2-cyclopenten-1-one;3-methyl-2-pentyl-2-cyclopenten-1-on;3-methyl-2-pentylcyclopent;Jasmone, dihydro-;Tetrahy-dropyrethrone
CAS:1128-08-1
MF:C11H18O
MW:166.26
EINECS:214-434-5
Product Categories:
Mol File:1128-08-1.mol
2-Pentyl-3-methyl-2-cyclopenten-1-one Structure
2-Pentyl-3-methyl-2-cyclopenten-1-one Chemical Properties
Boiling point 120-121 °C12 mm Hg(lit.)
density 0.916 g/mL at 25 °C(lit.)
FEMA 3763 | 3-METHYL-2-(N-PENTANYL)-2-CYCLOPENTEN-1-ONE
refractive index n20/D 1.479(lit.)
Fp 230 °F
storage temp. Store at -20°C
solubility DMSO:100.0(Max Conc. mg/mL);601.45(Max Conc. mM)
form clear liquid
color A colourless, slightly oily liquid with a floral-like odour
Specific Gravity0.914~0.916 (20/4℃)
Odorat 100.00 %. fresh outdoor jasmin myrrh woody spice herbal
Odor Typefloral
biological sourcesynthetic
JECFA Number1406
BRN 1906471
Major Applicationflavors and fragrances
Cosmetics Ingredients FunctionsPERFUMING
InChI1S/C11H18O/c1-3-4-5-6-10-9(2)7-8-11(10)12/h3-8H2,1-2H3
InChIKeyYCIXWYOBMVNGTB-UHFFFAOYSA-N
SMILESCCCCCC1=C(C)CCC1=O
LogP3.25
CAS DataBase Reference1128-08-1(CAS DataBase Reference)
NIST Chemistry ReferenceDihydrojasmone(1128-08-1)
EPA Substance Registry System2-Cyclopenten-1-one, 3-methyl-2-pentyl- (1128-08-1)
Safety Information
WGK Germany 2
RTECS GY7302000
TSCA TSCA listed
HS Code 29142990
Storage Class10 - Combustible liquids
toxicityThe acute oral LD50 in rats was reported as 2.5 g/kg (1.79-3.50 g/kg) (Keating, 1972). The acute dermal LD50 value in rabbits was reported as 5 g/kg (Keating, 1972).
MSDS Information
ProviderLanguage
2-Pentyl-3-methyl-2-cyclopenten-1-one English
SigmaAldrich English
ALFA English
2-Pentyl-3-methyl-2-cyclopenten-1-one Usage And Synthesis
AromaIntensely floral and fresh odor with fruity and somewhat Myrrh-like undertone. 2-Pentyl-3-methyl-2-cyclopenten-1-one is often described as the "closest to ci&Jasmone in odor". In proper dilution it has a pleasant, sweet, herbaceous-floral taste which is easily twisted towards a fruity note in presence of traces of fruity chemicals. It has an excellent softening effect upon the overly "chemical" fruit materials.
Uses in Perfume2-Pentyl-3-methyl-2-cyclopenten-1-one is widely used in perfume compositions, not only for artificial Jasmin and Bergamot, but in general as a floralizer in the more fruityfloral fragrance types: Ylang, Lily, Tuberose, Magnolia, etc. and it introduces a pleasant undertone in Citrus type fragrances.
Chemical Properties3-Methyl-2-(n-pentanyl)-2-cyclopenten-1-one has a fresh, fruity, jasmine odor with woody and herbal nuances.
Chemical Properties2-Pentyl-3-methyl-2-cyclopenten-1-one is a colorless, slightly viscous liquid with a typical jasmine odor, resembling that of the naturally occurring (Z)-jasmone. Dihydrojasmone is produced by an acid-catalyzed rearrangement of 4-methyl--decalactone, which is readily obtained by radical addition of 2-octanol to acrylic acid.
Dihydrojasmone is used in perfumery in jasmine bases and, more generally, in floral and fruity fragrances.
OccurrenceHas apparently not been reported to occur in nature.
Usesflavors and fragrances
PreparationHexyl bromide plus levulinic ester yields a lactone, which is reacted with polyphosphoric acid or phosphorus pentoxide to produce hydrojasmone.
DefinitionChEBI: 3-methyl-2-pentylcyclopent-2-en-1-one is a cyclic ketone.
Taste threshold valuesTaste characteristics at 10 ppm: sweet, floral, green, herbal with a citrus nuance.
Synthesis Reference(s)Canadian Journal of Chemistry, 56, p. 2301, 1978 DOI: 10.1139/v78-379
Journal of the American Chemical Society, 92, p. 7428, 1970 DOI: 10.1021/ja00728a029
2-Pentyl-3-methyl-2-cyclopenten-1-one Preparation Products And Raw materials
Raw materials6-Benzylaminopurine-->Jasmone-->Undecane
Tag:2-Pentyl-3-methyl-2-cyclopenten-1-one(1128-08-1) Related Product Information
2-methylcyclopentenone 2-Pentyl-3-methyl-2-cyclopenten-1-one 3-NONANONE DIHYDROJASMONE LACTONE DIHYDROJASMONE Methyl dihydrojasmonate 3-methylcyclopent-2-en-1-one PROSTAGLANDIN B1 2-PENTYL-2-CYCLOPENTEN-1-ONE 1-ETHYL-2-METHYLCYCLOPENTENE 1-Methylcyclopentene Jasmone 2-Cyclopenten-1-one 1-BUTYLCYCLOPENTENE 1,2-DIMETHYLCYCLOPENTENE 1-ETHYL-1-CYCLOPENTENE 2,3-DIMETHYL-2-CYCLOPENTEN-1-ONE di-Calciphor