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W390909

Sigma-Aldrich

Cyclohexanon

99.8%

Synonym(e):

Hexanon, Keto hexamethylene, Ketohexamethylene, Pimelic ketone, Sextone

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About This Item

Lineare Formel:
C6H10(=O)
CAS-Nummer:
108-94-1
Molekulargewicht:
98.14
FEMA-Nummer:
3909
Beilstein:
385735
EG-Nummer:
203-631-1
MDL-Nummer:
MFCD00001625
UNSPSC-Code:
12164502
PubChem Substanz-ID:
24901934
Flavis-Nummer:
7.148
NACRES:
NA.21

Biologische Quelle

synthetic

Agentur

meets purity specifications of JECFA

Dampfdichte

3.4 (vs air)

Dampfdruck

3.4 mmHg ( 20 °C)

Assay

99.8%

Form

liquid

Selbstzündungstemp.

788 °F

Expl.-Gr.

1.1 %, 100 °F
9.4 %

Brechungsindex

n20/D 1.450 (lit.)

bp

155 °C (lit.)

mp (Schmelzpunkt)

−47 °C (lit.)

Dichte

0.947 g/mL at 25 °C (lit.)

Anwendung(en)

flavors and fragrances

Dokumentation

see Safety & Documentation for available documents

Nahrungsmittelallergen

no known allergens

Organoleptisch

minty

SMILES String

O=C1CCCCC1

InChI

1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2

InChIKey

JHIVVAPYMSGYDF-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

Cyclohexanone is a cyclic ketone with a minty odor. It is reported to be present in volatile flavor fraction of kiwi fruit pulp and acerola fruit.

Anwendung


  • Structural Revision of Hyperibrin B and Hyperscabrones H and I by Biosynthetic Considerations, NMR Analysis, and Chemical Synthesis.: Cyclohexanone is utilized in the synthesis and structural revision of complex natural products, demonstrating its utility in biochemical research (Wang et al., 2021).

  • Biocatalytic conversion of cycloalkanes to lactones using an in-vivo cascade in Pseudomonas taiwanensis VLB120.: This study highlights the biocatalytic potential of Cyclohexanone in producing valuable lactones, contributing to advancements in green chemistry (Karande et al., 2018).

Haftungsausschluss

For R&D or non-EU Food use. Not for retail sale.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

111.2 °F - closed cup

Flammpunkt (°C)

44 °C - closed cup

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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GC-FTIR as a powerful tool for the characterization of flavor components in Kiwi.
Fischbock G, et al.
Microchimica Acta, 96(1), 249-257 (1988)
Application of fragment screening and merging to the discovery of inhibitors of the Mycobacterium tuberculosis cytochrome P450 CYP121.
Sean A Hudson et al.
Angewandte Chemie (International ed. in English), 51(37), 9311-9316 (2012-08-15)
Viktória Fábos et al.
Chemistry, an Asian journal, 7(11), 2629-2637 (2012-09-07)
Iron (and to a lesser extent manganese) in the wall of a 316 stainless steel (SS) reactor is responsible for the hydrogenation of cyclohexanone to cyclohexanol when using an aqueous formic acid solution under high temperature and pressure water (HTPW)
Michael Eddleston et al.
Toxicology, 294(2-3), 94-103 (2012-03-01)
Organophosphorus (OP) insecticide self-poisoning is responsible for about one-quarter of global suicides. Treatment focuses on the fact that OP compounds inhibit acetylcholinesterase (AChE); however, AChE-reactivating drugs do not benefit poisoned humans. We therefore studied the role of solvent coformulants in
Annhelen Lu et al.
Chemical communications (Cambridge, England), 48(78), 9699-9701 (2012-08-23)
The use of functional core-shell micelles as asymmetric catalytic nanoreactors for organic reactions in water is presented. An unprecedented increase in rate of reaction was achieved, which is proposed to be associated with the ability of the nanostructures to effectively
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