Skip to Content
Merck
CN

Key Documents

View All Documentation

410896

2-Hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone

98%

Synonym(s):

1-[4-(2-Hydroxyethoxy)phenyl]-2-hydroxy-2-methyl-1-propan-1-one, 2-Hydroxy-1-[4-(2-hydroxyethoxy)phenyl]-2-methyl-1-propanone, 2-Hydroxy-2-methyl-1-[4-(2-hydroxyethoxy)phenyl]propan-1-one, 4-(2-Hydroxyethoxy)phenyl 2-hydroxy-2-propyl ketone

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
HOCH2CH2OC6H4COC(CH3)2OH
CAS Number:
106797-53-9
Molecular Weight:
224.25
NACRES:
NA.23
PubChem Substance ID:
24865712
UNSPSC Code:
12162002
MDL number:
MFCD00085267
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

200

assay

98%

mp

88-90 °C (lit.)

SMILES string

CC(C)(O)C(=O)c1ccc(OCCO)cc1

InChI

1S/C12H16O4/c1-12(2,15)11(14)9-3-5-10(6-4-9)16-8-7-13/h3-6,13,15H,7-8H2,1-2H3

InChI key

GJKGAPPUXSSCFI-UHFFFAOYSA-N

Application

2-Hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone can be used as a photo-initiator to synthesize:
  • Polyacrylamide-grafted chitosan nanoparticles by copolymerization of acrylamide and chitosan nanoparticles.
  • Hydrophobic polyurethane sponge through thiol–ene Click reaction.

pictograms

Environment
GHS09

hcodes

H411

Hazard Classifications

Aquatic Chronic 2

Storage Class

11 - Combustible Solids

flash_point_f

not determined

flash_point_c

not determined

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000509769
0000509769
MKCX9610
MKCX2056
0000352457

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Articles

Hydrogels for Biomedical Applications

Discover hydrogels, biocompatible materials for drug delivery, tissue engineering, wound care, and 3D bioprinting in innovative biomedical applications

Related Content

Free Radical Initiators

Photoinitiators convert light energy into chemical energy for initiating species formation in formulations, essential for various applications.

Deepak Kumar et al.
Cell transplantation, 25(12), 2213-2220 (2016-07-28)
Nucleus pulposus (NP) tissue damage can induce detrimental mechanical strain on the biomechanical performance of intervertebral discs (IVDs), causing subsequent disc degeneration. A novel, photocurable, injectable, synthetic polymer hydrogel (pHEMA-co-APMA grafted with PAA) has already demonstrated success in encapsulating and
Rami El Assal et al.
Scientific reports, 6, 39144-39144 (2016-12-23)
Cancer cells have been increasingly grown in pharmaceutical research to understand tumorigenesis and develop new therapeutic drugs. Currently, cells are typically grown using two-dimensional (2-D) cell culture approaches, where the native tumor microenvironment is difficult to recapitulate. Thus, one of
Jiangya Ma et al.
Carbohydrate polymers, 151, 565-575 (2016-07-31)
In the present work, a new flocculant, polyacrylamide-grafted chitosan nanoparticles (NCS-g-PAM), was synthesized by the copolymerization of acrylamide (AM) and chitosan nanoparticle (NCS) under ultraviolet irradiation using 2-hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone as photo-initiator. The NCS was prepared by the ionic gelation between chitosan
View All Related Papers

Global Trade Item Number

SKUGTIN
410896-50G04061835562978
410896-10G04061832019642
410896-5MG04061833238776