Saltar al contenido
Merck

333840

Sigma-Aldrich

Dicyclohexylacetic acid

99%

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula lineal:
(C6H11)2CHCO2H
Número de CAS:
Peso molecular:
224.34
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

99%

form

solid

mp

139-141 °C (lit.)

functional group

carboxylic acid

SMILES string

OC(=O)C(C1CCCCC1)C2CCCCC2

InChI

1S/C14H24O2/c15-14(16)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h11-13H,1-10H2,(H,15,16)

Inchi Key

PGGMEZOUAPIYOY-UHFFFAOYSA-N

Application

Dicyclohexylacetic acid was used in the synthesis of 2,2-dicyclohexyl-1-(4′-methyl)-phenylethanone. It was also used in the synthesis of catena-poly [[trimethyltin (IV)]--2, 2-dicyclohexylacetato-2O: O′].

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number

¿No ve la versión correcta?

Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Excited precursor reactivity, fast 1, 2-H shifts, and diffusion-controlled methanol insertion in 1, 2-Diphenylalkylidenes.
Motschiedler K, et al.
The Journal of Organic Chemistry, 64(14), 5139-5147 (1999)
catena-Poly [[trimethyltin (IV)]--2, 2-dicyclohexylacetato-2O: O′].
Cheikh AKD, et al.
Acta Crystallographica Section E, Structure Reports Online, 63(1), m258-m260 (2006)
Mohamed H Mohamed et al.
Journal of colloid and interface science, 395, 104-110 (2013-02-05)
Tensiometry was used to provide estimates of the critical micelle concentration (cmc) values for three sources of naphthenic acids (NAs) and three examples of single component NAs (S1-S3) in aqueous solution at pH 10.5 and 295 K. Two commercially available
Mette Kristensen et al.
Journal of chromatography. A, 1601, 21-26 (2019-05-13)
Gas-chromatography (GC) analysis of carboxylic acids is limited by the high polarity and low volatility of most of these compounds. Boron trifluoride (BF3) mediated alkylation reactions is one of the most commonly used derivatization methods for making carboxylic acids GC
Dieter Schemeth et al.
Analytica chimica acta, 1038, 182-190 (2018-10-04)
In this study, we focus on isolation and fractionation strategies by solid phase extraction (SPE) for a broad range of environmentally related organic acids. These emerging potential contaminants are primary degradation products of spilled petrogenic compounds but little attention has

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico