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fruity cyclopentanone

Fruity cyclopentanone is a medium-strength fragrance compound with a fruity, floral, and lactonic scent profile used mainly in perfumery.
Chemical Structure

General Material Description

Fruity cyclopentanone, also known by synonyms such as 2,2,5-trimethyl-5-pentylcyclopentanone and commercial names like Veloutone, is a synthetic organic compound primarily utilized as a fragrance ingredient. This molecule features a cyclopentanone core substituted with methyl and pentyl groups, yielding the molecular formula C13H24O and a molecular weight of approximately 196.33 g/mol. It presents as a stable, colorless liquid with a distinctive medium-strength odor characterized by fruity notes reminiscent of peach and apricot, complemented by floral jasmine, lactonic nuances, and a hint of lavender. The compound is accessible primarily through synthetic routes and is listed under PubChem (CID 103402). Its stability and complex scent profile make it highly valuable in fragrance formulations aiming for soft floral and fruity characteristics.

Occurrence, Applicability & Potential Uses

Fruity cyclopentanone does not occur naturally in significant quantities and is synthesized for commercial use predominantly as a fragrance agent within fine fragrances and personal care products. It provides a versatile floral and fruity character reminiscent of jasmine, honeysuckle, tuberose, lilac, and woody notes, enhancing diverse perfume categories. Under the IFRA (International Fragrance Association, Global) Code of Practice, its use is recommended up to 2% concentration in fragrance concentrates. This compound is not intended for flavor applications. Its stability contributes to long-lasting olfactory effects in formulations, expanding its applicability to products such as shampoos, soaps, and shower gels, where it also imparts herbal and lavender nuances.

Physico-Chemical Properties Summary

Fruity cyclopentanone exhibits a moderate volatility with a vapor pressure of approximately 0.026 mmHg at 25°C and a relatively high estimated logP value of 4.16, indicating substantial lipophilicity. Its flash point, measured by the Tag Closed Cup method, is around 194°F (90°C), suggesting moderate flammability under heat. The compound is soluble in alcohol and has limited water solubility estimated at 8.956 mg/L at 25°C. Its chemical stability allows usage in multiple product types at trace to low-percent levels without significant degradation. These properties influence formulation strategies, favoring incorporation into alcohol-based perfume bases and ensuring persistence on skin or substrates without rapid evaporation or breakdown.

FAQ

What is fruity cyclopentanone and what are its main characteristics?
Fruity cyclopentanone, also known as 2,2,5-trimethyl-5-pentylcyclopentanone or by trade names such as Veloutone, is a synthetic fragrance compound notable for its medium-strength, fruity odor. Its scent profile includes nuances of peach, apricot, jasmine, and a subtle hint of lavender, combined with lactonic and floral notes. It appears as a colorless liquid with good chemical stability, making it a valued odorant in perfumery.
How is fruity cyclopentanone used and in what types of products?
This compound is used predominantly as a perfuming agent in fragrance formulations. Its stable, versatile scent makes it suitable for fine fragrances as well as personal care products like shampoos, soaps, and shower gels. Fruity cyclopentanone contributes fruity, floral, and woody notes and blends well with ingredients such as honeysuckle, lilac, and tuberose. It is recommended for use up to 2% in fragrance concentrates according to IFRA (Global) guidelines.
What regulations and safety considerations apply to fruity cyclopentanone?
Fruity cyclopentanone is classified as a fragrance material with no specific hazard classifications under OSHA HCS (29 CFR 1910). It has undergone safety assessment by RIFM and is subject to IFRA standards, permitting use up to defined levels in fragrances. While there is no indication for flavor usage, safety data recommend handling as per standard good manufacturing practices. Its regulatory references include registration in ECHA’s REACH database (EU) and listing in chemical inventories such as the EPA TSCA registry.

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Other Information

General Material Information

Preferred name fruity cyclopentanone
Trivial Name 2,2,5-Trimethyl-5-pentylcyclopentanone
Short Description veloutone (Firmenich)
Formula C13 H24 O
CAS Number 65443-14-3
Deleted CAS Number 193818-98-3
ECHA Number 265-779-3
FDA UNII BN3YZU63MN
Nikkaji Number J23.228I
xLogP3-AA 4.20 (est)
NMR Predictor External link
Synonyms
  • cyclopentanone, 2,2,5-trimethyl-5-pentyl-
  • 2-pentyl-2,5,5-trimethyl cyclopentanone
  • 2-pentyl-2,5,5-trimethylcyclopentanone
  • trimethyl pentyl cyclopentanone
  • 2,2,5-trimethyl-5-pentyl cyclopentan-1-one
  • 2,2,5-trimethyl-5-pentyl cyclopentanone
  • (±)-2,2,5-trimethyl-5-pentyl-1-cyclopentanone
  • 2,2,5-trimethyl-5-pentylcyclopentan-1-one
  • velotonia (Indukern)
  • veloutone (Firmenich)
  • 2,2,5-trimethyl-5-pentylcyclopentan-1-one
  • 2,2,5-Trimethyl-5-pentylcyclopentanone
  • Veloutone
  • Velouton

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 196.33348083496
Acid Value 1 max KOH/g
Vapor Pressure 0.026 mmHg @ 25 °C
Flash Point TCC Value 90 °C TCC
logP (o/w) 4.164 est
Solubility
alcohol Yes
water, 8.956 mg/L @ 25 °C (est) Yes
Stability
APC: traces - 1% Unspecified
candle: traces - 2% Unspecified
detergent: traces - 0.5% Unspecified
fine fragrances: traces - 0.5% Unspecified
shampoo: traces - 2% Unspecified
shower gel: traces - 2% Unspecified
soap: traces - 2% Unspecified
softener: traces - 0.5% Unspecified

Organoleptic Properties

Odor Type: Fruity
fruity, peach, apricot, jasmin, lactonic, herbal, lavender
Odor strength medium
Substantivity 12 hour(s) at 100.00 %
Luebke, William tgsc, (1988) At 100.00 %. fruity peach apricot jasmin lactonic herbal lavender
A jasmine, lactonic and fruity note reminiscent of peach and apricot with a hint of lavender. Has broad use because of its exceptional stability and makes a wonderful soft floral note in jasmine, tuberose, honeysuckle creations as well as muguet lilac and fruity notes. Jasmin, lactonic and fruity odour. Reminiscent of peach and apricot with a suggestion of lavender
Firmenich describe it as “A jasmine, lactonic and fruity note reminiscent of peach and apricot with a hint of lavender. Has broad use because of its exceptional stability and makes a wonderful soft floral note in jasmine, tuberose, honeysuckle creations as well as muguet lilac and fruity notes. It gives interesting effects in lavender and herbal perfumes.” Writing in 1985, Arcadi Boix Camps describes Veloutone as having “a profound, smooth, floral note, which combines with a large number of diverse notes. Its blends with Hedione, Vertofix Coeur … are excellent.” Floral-jasmine, fruity-peach, and apricot, lactonic, lavender
General comment Fruit peach, apricot, lactone flavor with notes of jasmine and lavender

Potential Uses

Applications
Odor purposes Apricot , Fruit , Herbal , Honeysuckle , Jasmin , Lavender , Lilac , Lily of the valley , Peach , Spice , Tuberose , Woody
Cosmetic purposes Perfuming agents

Safety Information

Safety information

Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Pictogram
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in use information

Category:
fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for fruity cyclopentanone usage levels up to:
2.0000 % in the fragrance concentrate.
Recommendation for fruity cyclopentanone flavor usage levels up to:
not for flavor use.

Safety references

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):65443-14-3
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :103402
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
2,2,5-trimethyl-5-pentylcyclopentan-1-one
Chemidplus:0065443143