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W391018

Sigma-Aldrich

Cyclopentanone

≥99%, FG

Synonyme(s) :

Adipic ketone, Dumasin, Ketopentamethylene

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About This Item

Formule linéaire :
C5H8(=O)
Numéro CAS:
120-92-3
Poids moléculaire :
84.12
Numéro FEMA:
3910
Numéro Beilstein :
605573
Numéro CE :
204-435-9
Numéro MDL:
MFCD00001409
Code UNSPSC :
12164502
ID de substance PubChem :
24901935
Numéro Flavis :
7.149
Nomenclature NACRES :
NA.21

Source biologique

synthetic

Niveau de qualité

400

Qualité

FG
Fragrance grade
Halal
Kosher

Agence

follows IFRA guidelines
meets purity specifications of JECFA

Conformité réglementaire

EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 110

Pureté

≥99%

Indice de réfraction

n20/D 1.437 (lit.)

Point d'ébullition

130-131 °C (lit.)

Pf

−51 °C (lit.)

Densité

0.951 g/mL at 25 °C (lit.)

Application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

Allergène alimentaire

no known allergens

Allergène de parfum

no known allergens

Propriétés organoleptiques

minty

Chaîne SMILES 

O=C1CCCC1

InChI

1S/C5H8O/c6-5-3-1-2-4-5/h1-4H2

Clé InChI

BGTOWKSIORTVQH-UHFFFAOYSA-N

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Catégories apparentées

Description générale

Cyclopentanone is a cyclic ketone that occurs in allium species, beef, cheese, and chicken. It is generally used as a fragrance ingredient in fragrances and in non-cosmetic products.

Application


  • High-oxygen-modified atmospheric packaging delays flavor and quality deterioration in fresh-cut broccoli.: This research investigates the impact of high-oxygen-modified atmospheric packaging on the preservation of fresh-cut broccoli. Cyclopentanone is identified as a significant compound in the aroma profile, contributing to the understanding of packaging technologies that maintain food quality and extend shelf life. (He et al., 2024).

  • Selective production of methylindan and tetralin with xylose or hemicellulose.: The study focuses on the selective production of methylindan and tetralin using xylose or hemicellulose, with Cyclopentanone playing a key role in the catalytic processes. This research provides insights into sustainable chemical production from biomass-derived feedstocks. (Zou et al., 2024).

  • Synthesis of Hydroxylamine via Ketone-Mediated Nitrate Electroreduction.: This paper presents a novel method for synthesizing hydroxylamine through ketone-mediated nitrate electroreduction, utilizing Cyclopentanone. The findings demonstrate the versatility of Cyclopentanone in electrochemical synthesis and its potential for green chemistry applications. (Jia et al., 2024).


Autres remarques

Handle and store under inert gas.

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Warning

Mentions de danger

H226,H315,H319

Classification des risques

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

86.0 °F - closed cup

Point d'éclair (°C)

30 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Fragrance material review on cyclopentanone.
Scognamiglio J, et al.
Food And Chemical Toxicology, 50, S608-S612 (2012)
Pragya Verma et al.
The Journal of organic chemistry, 76(14), 5606-5613 (2011-06-02)
The density functional theory investigation on the mechanism of NHC-catalyzed cycloannulation reaction of the homoenolate derived from butenal with pentenone is studied. The M06-2X/6-31+G** and B3LYP/6-31+G** levels of theory, including the effect of continuum solvation in dichloromethane and tetrahydrofuran, are
Na Lin et al.
Physical chemistry chemical physics : PCCP, 14(10), 3669-3680 (2012-02-09)
We present a theoretical study of vibrationally resolved circular dichroism spectra, both in the adiabatic and non-adiabatic frameworks, with a full account of Franck-Condon and Herzberg-Teller vibrational contributions for the former. Model calculations have been performed on 2(R)-deuteriocyclopentanone, whose chirality
Mohi Uddin Jewel et al.
Molecules (Basel, Switzerland), 25(5) (2020-03-04)
Fully inkjet-printed device fabrication is a crucial goal to enable large-area printed electronics. The limited number of two-dimensional (2D) material inks, the bottom-gated structures, and the low current on/off ratio of thin-film transistors (TFTs) has impeded the practical applications of
Anqi Ma et al.
Organic letters, 12(16), 3634-3637 (2010-08-14)
The O-TMS-protected diphenylprolinol-catalyzed cascade double Michael addition reactions of alpha,beta-unsaturated aldehydes with a beta-keto ester bearing a highly electron-deficient olefin unit occur smoothly to afford polysubstituted cyclopentanones. This process allows formation of four contiguous stereocenters in the cyclopentanone ring in
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