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W391018

Sigma-Aldrich

Cyclopentanone

≥99%, FG

Sinonimo/i:

Adipic ketone, Dumasin, Ketopentamethylene

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About This Item

Formula condensata:
C5H8(=O)
Numero CAS:
Peso molecolare:
84.12
Numero FEMA:
3910
Beilstein:
605573
Numero CE:
Numero MDL:
Codice UNSPSC:
12164502
ID PubChem:
Numero Flavis:
7.149
NACRES:
NA.21

Origine biologica

synthetic

Livello qualitativo

Grado

FG
Fragrance grade
Halal
Kosher

agenzia

follows IFRA guidelines
meets purity specifications of JECFA

Conformità normativa

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

Saggio

≥99%

Indice di rifrazione

n20/D 1.437 (lit.)

P. eboll.

130-131 °C (lit.)

Punto di fusione

−51 °C (lit.)

Densità

0.951 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

no known allergens

Organolettico

minty

Stringa SMILE

O=C1CCCC1

InChI

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

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Descrizione generale

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.

Applicazioni


  • 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).


Altre note

Handle and store under inert gas.

Pittogrammi

FlameExclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

86.0 °F - closed cup

Punto d’infiammabilità (°C)

30 °C - closed cup

Dispositivi di protezione individuale

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


Certificati d'analisi (COA)

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Fragrance material review on cyclopentanone.
Scognamiglio J, et al.
Food And Chemical Toxicology, 50, S608-S612 (2012)
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
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
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
Mohi Uddin Jewel et al.
Molecules (Basel, Switzerland), 25(5) (2020-03-04)
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