Skip to Content
Merck
CN

405612

1-Hydroxycyclohexyl phenyl ketone

99%

Synonym(s):

(1-Hydroxycyclohexyl)phenylmethanone, 1-Benzoyl-1-hydroxycyclohexane, 1-Benzoylcyclohexanol

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
HOC6H10COC6H5
CAS Number:
Molecular Weight:
204.26
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
213-426-9
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

1-Hydroxycyclohexyl phenyl ketone, 99%

InChI key

QNODIIQQMGDSEF-UHFFFAOYSA-N

InChI

1S/C13H16O2/c14-12(11-7-3-1-4-8-11)13(15)9-5-2-6-10-13/h1,3-4,7-8,15H,2,5-6,9-10H2

SMILES string

OC1(CCCCC1)C(=O)c2ccccc2

assay

99%

bp

175 °C/15 mmHg (lit.)

mp

47-50 °C (lit.)

Quality Level

General description

1-Hydroxycyclohexyl phenyl ketone is a photoinitiator (PI) molecule that can be used in chain transfer polymerization. PI can be incorporated in the polymeric matrix by the addition of a chromophore as a pendant group. It may be used as a component that facilitates UV curing and also as a base material in the formation of the block and grafted copolymers.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

327.2 °F - closed cup

flash_point_c

164 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Wei Yu et al.
Materials (Basel, Switzerland), 12(23) (2019-12-01)
Polymeric microparticles were produced following a three-step procedure involving (i) the production of an aqueous nanoemulsion of tri and monofunctional acrylate-based monomers droplets by an elongational-flow microemulsifier, (ii) the production of a nanosuspension upon the continuous-flow UV-initiated miniemulsion polymerization of
Stress Relaxation by Addition- Fragmentation Chain Transfer in Highly Cross-Linked Thiol- Yne Networks
Park HY, et al.
Macromolecules, 43(24), 10188-10190 (2010)
Furqan A Maulvi et al.
International journal of pharmaceutics, 581, 119279-119279 (2020-04-03)
Loading of gatifloxacin in contact lenses affects critical lens properties (optical and swelling) owing to drug precipitation in the contact lens matrix. The presence of Pluronic® F-68 in the packaging solution creates in-situ micelles in the contact lens to dissolve
Shuhong Duan et al.
Membranes, 9(12) (2019-12-11)
The effect of carbonic anhydrase (CA) on the separation performance of thin poly(amidoamine) (PAMAM) dendrimer/poly(ethylene glycol) (PEG) hybrid membranes was investigated. CA, a type of enzyme, was used to promote CO2 hydration and dehydration reactions and to assess whether these
Synthesis and characterization of novel well-defined end-functional macrophotoinitiator of poly (MMA) by ATRP
Degirmenci M
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 42(1), 21-30 (2005)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service