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Documenti fondamentali

44028

Supelco

Cyclohexene

analytical standard, ≥99.5% (GC)

Sinonimo/i:

Tetrahydrobenzene

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About This Item

Formula empirica (notazione di Hill):
C6H10
Numero CAS:
Peso molecolare:
82.14
Beilstein:
906737
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Densità del vapore

2.8 (vs air)

Tensione di vapore

160 mmHg ( 20 °C)

Saggio

≥99.5% (GC)

Temp. autoaccensione

590 °F

Durata

limited shelf life, expiry date on the label

contiene

~0.01% 2,6-di-tert-butyl-4-methylphenol as stabilizer

Limite di esplosione

5 %

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.446 (lit.)
n20/D 1.446

P. ebollizione

83 °C (lit.)

Punto di fusione

−104 °C (lit.)

Densità

0.811 g/mL at 25 °C (lit.)

applicazioni

environmental
petroleum

Formato

neat

Stringa SMILE

C1CCC=CC1

InChI

1S/C6H10/c1-2-4-6-5-3-1/h1-2H,3-6H2
HGCIXCUEYOPUTN-UHFFFAOYSA-N

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Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

1.4 °F

Punto d’infiammabilità (°C)

-17 °C

Dispositivi di protezione individuale

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


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Certificati d'analisi (COA)

Lot/Batch Number

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Hexanal 98%

Sigma-Aldrich

115606

Hexanal

Cyclohexanone ACS reagent, ≥99.0%

Sigma-Aldrich

398241

Cyclohexanone

Bromina reagent grade

Sigma-Aldrich

207888

Bromina

Cyclohexanone analytical standard

Supelco

02482

Cyclohexanone

Hexyl acetate analytical standard

Supelco

25539

Hexyl acetate

Amelia W Ray et al.
The journal of physical chemistry. A, 116(25), 6720-6730 (2012-05-29)
Earlier synchrotron photoionization mass spectrometry experiments suggested a prominent ring-opening channel in the OH-initiated oxidation of cyclohexene, based on comparison of product photoionization spectra with calculated spectra of possible isomers. The present work re-examines the OH + cyclohexene reaction, measuring
Jan Lennard Wolf et al.
Physical chemistry chemical physics : PCCP, 13(23), 10952-10964 (2011-03-29)
The gas-phase ozonolysis of cyclic-alkenes (1-methyl-cyclohexene, methylene-cyclohexane, α-pinene, β-pinene) is studied with respect to the pressure dependent formation of secondary organic aerosol (SOA). We find that SOA formation is substantially suppressed at lower pressures for all alkenes under study. The
Hiroshi Nagase et al.
Bioorganic & medicinal chemistry letters, 22(15), 5071-5074 (2012-06-30)
To clarify the essential structures of an opioid κ receptor selective agonist, nalfurafine, for binding to the κ receptor, we designed and synthesized some nalfurafine derivatives and the decahydro(iminoethano)phenanthrene derivatives with a cyclohexene moiety as a surrogate for the phenol
Zhong Chen et al.
Journal of Asian natural products research, 15(1), 53-58 (2013-01-18)
A new polyoxygenated cyclohexene bonianol A (1) and another new polyoxygenated seco-cyclohexene bonianol B (2) were isolated from the leaves of Uvaria boniana, and their structures were established on the basis of spectroscopic methods including IR, HR-ESI-MS, 1D, and 2D
Amit Aggarwal et al.
Macromolecular rapid communications, 33(14), 1220-1226 (2012-04-21)
Self-organized organic nanoparticles (ONP) are adaptive to the environmental reaction conditions. ONP of fluorous alkyl iron(III) porphyrin catalytically oxidize cyclohexene to the allylic oxidation products. In contrast, the solvated metalloporphyrin yields both allylic oxidation and epoxidation products. The ONP system

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