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Sigma-Aldrich

Dicyclohexylacetic acid

99%

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About This Item

Linear Formula:
(C6H11)2CHCO2H
CAS Number:
52034-92-1
Molecular Weight:
224.34
MDL number:
MFCD00075017
UNSPSC Code:
12352100
PubChem Substance ID:
24860190
NACRES:
NA.22

Quality Level

100

assay

99%

form

solid

mp

139-141 °C (lit.)

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

Related Categories

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
GHS07

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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)
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)
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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
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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

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