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44113

Supelco

Cyclohexanol

analytical standard

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About This Item

Fórmula linear:
C6H11OH
Número CAS:
108-93-0
Peso molecular:
100.16
Beilstein:
906744
Número CE:
203-630-6
Número MDL:
MFCD00003855
Código UNSPSC:
85151701
ID de substância PubChem:
329756453
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

densidade de vapor

3.5 (vs air)

pressão de vapor

0.98 mmHg ( 25 °C)

Ensaio

≥98.5% (GC)

temperatura de autoignição

572 °F

prazo de validade

limited shelf life, expiry date on the label

Lim. expl.

12.25 %

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

Impurezas

≤0.5% cyclohexanone (GC)
≤0.5% water

índice de refração

n20/D 1.465 (lit.)

pb

160-161 °C (lit.)

pf

20-22 °C (lit.)

densidade

0.948 g/mL at 25 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

formato

neat

cadeia de caracteres SMILES

OC1CCCCC1

InChI

1S/C6H12O/c7-6-4-2-1-3-5-6/h6-7H,1-5H2

chave InChI

HPXRVTGHNJAIIH-UHFFFAOYSA-N

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Aplicação

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

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

147.2 °F - closed cup - DIN 51794

Ponto de fulgor (°C)

64 °C - closed cup - DIN 51794

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
BCCK8676
BCCF4439
BCBX8823
BCBX5243
BCBQ9798V

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Sigma-Aldrich

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Supelco

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Sigma-Aldrich

709972

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Sigma-Aldrich

125431

Cyclohexene

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Sigma-Aldrich

C102652

2-Cyclohexen-1-ol

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Journal of agricultural and food chemistry, 62(33), 8500-8507 (2014-07-30)
Hexanal, 2-heptenal, and nonanal were identified as relevant reaction products formed in the course of the lipid peroxidation of heated peanut oil. For the identification of potential amino acid side chain adducts, kinetic studies between N(α)-benzoylglycyl-l-lysine as a model for
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Microfluidic systems with monolithic columns have been developed for preconcentration and on-chip labeling of model proteins. Monoliths were prepared in microchannels by photopolymerization, and their properties were optimized by varying the composition and concentration of the monomers to improve flow
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Chemistry (Weinheim an der Bergstrasse, Germany), 20(47), 15618-15624 (2014-10-07)
The present article describes novel oxidative protocols for direct esterification of alcohols. The protocols involve successful demonstrations of both "cross" and "self" esterification of a wide variety of alcohols. The cross-esterification proceeds under a simple transition-metal-free condition, containing catalytic amounts
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