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44113

Supelco

Cyclohexanol

analytical standard

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About This Item

Formule linéaire :
C6H11OH
Numéro CAS:
108-93-0
Poids moléculaire :
100.16
Numéro Beilstein :
906744
Numéro CE :
203-630-6
Numéro MDL:
MFCD00003855
Code UNSPSC :
85151701
ID de substance PubChem :
329756453
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Densité de vapeur

3.5 (vs air)

Pression de vapeur

0.98 mmHg ( 25 °C)

Pureté

≥98.5% (GC)

Température d'inflammation spontanée

572 °F

Durée de conservation

limited shelf life, expiry date on the label

Limite d'explosivité

12.25 %

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Impuretés

≤0.5% cyclohexanone (GC)
≤0.5% water

Indice de réfraction

n20/D 1.465 (lit.)

Point d'ébullition

160-161 °C (lit.)

Pf

20-22 °C (lit.)

Densité

0.948 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Chaîne SMILES 

OC1CCCCC1

InChI

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

Clé InChI

HPXRVTGHNJAIIH-UHFFFAOYSA-N

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Catégories apparentées

Application

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

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

147.2 °F - closed cup - DIN 51794

Point d'éclair (°C)

64 °C - closed cup - DIN 51794

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Certificats d'analyse (COA)

Lot/Batch Number
BCCF4439
BCBX8823
BCBX5243
BCBQ9798V
BCBL4223

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Martin Globisch et al.
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
Eric L Kendall et al.
Biomicrofluidics, 8(4), 044109-044109 (2014-11-08)
A technique for microfluidic, pH modulated DNA capture and purification using chitosan functionalized glycidyl methacrylate monoliths is presented. Highly porous polymer monoliths are formed and subsequently functionalized off-chip in a batch process before insertion into thermoplastic microchannels prior to solvent
Roy Bogseth et al.
Journal of the American Society for Mass Spectrometry, 25(11), 1987-1990 (2014-09-25)
Simple alcohols formed protonated acetonitrile adducts containing up to two acetonitrile molecules when analyzed by ESI or APCI in the presence of acetonitrile in the solvent. These acetonitrile adducts underwent dissociation to form a nitrilium ion, also referred to as
Ritwika Ray et al.
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
Rui Yang et al.
Analytical and bioanalytical chemistry, 407(3), 737-747 (2014-07-12)
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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