Ciclohexanol 99 %, Thermo Scientific Chemicals
Ciclohexanol 99 %, Thermo Scientific Chemicals
Ciclohexanol 99 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Ciclohexanol 99 %, Thermo Scientific Chemicals

CAS: 108-93-0 | C6H12O | 100.161 g/mol
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Cantidad:
100 mL
500 mL
2500 mL
Número de catálogo A17576.AE
también denominado A17576-AE
Precio (EUR)
27,10
Each
Cantidad:
100 mL
Pedido a granel o personalizado
Precio (EUR)
27,10
Each
Identificadores químicos
CAS108-93-0
IUPAC Namecyclohexanol
Molecular FormulaC6H12O
InChI KeyHPXRVTGHNJAIIH-UHFFFAOYSA-N
SMILESOC1CCCCC1
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EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥98.5%
Identification (FTIR)Conforms
Cyclohexanol is used in making soaps, dry cleaning agents and plasticizers. It acts as a solvent for rubber, resins, nitrocellulose, metallic soaps, oils, esters and ethers. It is used in the preparation of adipic acid, hexamethylene diamine, cyclohexanone and caprolactam. It acts as a soap stabilizing agent, disinfection medicated soap and detergent emulsion. It is also useful for paint blending agent, leather degreasing agent and polishes.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
El ciclohexanol se utiliza en la fabricación de jabones, productos de limpieza en seco y plastificadores. Actúa como disolvente para caucho, resinas, nitrocelulosa, jabones metálicos, aceites, ésteres y éteres. Se utiliza en la preparación de ácido adípico, diamina de hexametileno, ciclohexanona y caprolactam. Actúa como agente estabilizador de jabón, jabón medicinal de desinfección y emulsión detergente. También es útil para el agentes de mezcla de pintura, desengrasante de cuero y abrillantadores.

Solubilidad
Miscible con etanol, éter etílico, acetona, cloroformo, acetato de etilo, aceite de linaza y benceno. Ligeramente miscible con agua fría.

Notas
Higroscópico. Incompatible con agentes oxidantes fuertes, peróxido de hidrógeno y ácido nítrico.
RUO – Research Use Only

General References:

  1. Cyclohexyl esters can be used to protect carboxylic acids, including aspartate residues in peptide synthesis, resulting in reduced aspartimide formation during acidic or basic reactions: Synthesis, 361 (1992). They are relatively stable to TFA but can be readily cleaved by TfOH or HF: Int. J. Pept. Protein Res., 13, 418 (1979); Tetrahedron Lett., 4033 (1979); Chem. Pharm. Bull., 34, 864 (1986). See also 2,4-Dimethyl-3-pentanol, B20821 .
  2. Schemeth, D.; Noël, J. C.; Jakschitz, T.; Rainer, M.; Tessadri, R.; Huck, C. W.; Bonn, G. K. Poly(N-vinylimidazole/ethylene glycol dimethacrylate) for the purification and isolation of phenolic acids. Anal. Chim. Acta 2015, 885, 199-206.
  3. Zhang, P.; Deng, J.; Mao, J.; Li, H.; Wang, Y. Selective aerobic oxidation of alcohols by a mesoporous graphitic carbon nitride-hydroxyphthalimide system under visible-light illumination at room temperature. Chin. J. Catal. 2015, 36 (9), 1580-1586.