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413437

2-[3-(2H-Benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate

Name: 2-[3-(2<I>H</I>-Benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate
Brand: ALDRICH

99%

Synonym(s):

2-[2-Hydroxy-5-[2-(methacryloyloxy)ethyl]phenyl]-2H-benzotriazole

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About This Item

Empirical Formula (Hill Notation):

C₁₈H₁₇N₃O₃

CAS Number:

96478-09-0

Molecular Weight:

323.35

MDL number:

MFCD01080772

NACRES:

NA.23

PubChem Substance ID:

24865865

UNSPSC Code:

12162002

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Properties

Quality Level

200

assay

99%

form

solid

mp

96-98 °C (lit.)

SMILES string

CC(=C)C(=O)OCCc1ccc(O)c(c1)-n2nc3ccccc3n2

InChI

1S/C18H17N3O3/c1-12(2)18(23)24-10-9-13-7-8-17(22)16(11-13)21-19-14-5-3-4-6-15(14)20-21/h3-8,11,22H,1,9-10H2,2H3

InChI key

VCYCUECVHJJFIQ-UHFFFAOYSA-N

Description

General description

2-[3-(2H-Benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate is an organic compound that belongs to the class of acrylate monomers. It is commonly used as a UV absorber or stabilizer in polymers, coatings, adhesives, intraocular lenses, and other materials to protect them from the harmful effects of UV radiation.

Application

2-[3-(2H-Benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate can be used:

To prepare a polymer material by copolymerization with 2-hydroxy-4-acryloyloxybenzophenone (HABP). The synthesized polymer can be applied to cotton fabric for UV protection.
In the preparation of ultraviolet (UV) protective textiles. It is grafted onto the fabric via polymerization to create a UV-protective coating.
As a monomer in synthesizing fluoroalkyl end-capped oligomers with good surface-active properties.
It is also used as a UV absorber (UVAs) in intraocular lenses.

Hazard Classifications

Aquatic Chronic 4

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Articles

Continuous Flow Monomer Synthesis

Monomers for ophthalmic use aim for purity, reliability, and comfort, driving innovation for affordable contact lenses.

SYNTHESIS AND APPLICATIONS OF NOVEL FLUOROALKYL END-CAPPED OLIGOMERS CONTAINING 3,5-DIMETHYL-4-HYDROXYBENZYL AND 3-(2H-BENZOTRIAZOL-2-yl)-4-HYDROXYPHENYL SEGMENTS

Hideo Sawada, et al

International Journal of Polymeric Materials and Polymeric Biomaterials, 4, 311-332 (2005)

Analysis of Polymeric UV Absorber (Tinuvin 213) Using LDI-TOFMS: Solvent Effect in Sample Preparation

Im SH and Choi SS

Bull. Korean Chem. Soc., 32 (6), 2093-2093 (2011)

Enhancing enzyme stability against TiO2-UV induced inactivation.

Bhalchandra S Lele et al.

Biomacromolecules, 6(1), 475-482 (2005-01-11)

The use of enzymes in conjunction with inorganic photocatalysts requires stability against photooxidation. In this paper, we describe enhanced stabilization of a model enzyme, chymotrypsin, to photooxidation driven by titanium dioxide exposed to ultraviolet light (TiO(2)-UV). Stabilization is achieved conjugating

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Global Trade Item Number

SKU	GTIN
413437-500G	04061835383061
413437-100G	04061832928845
413437-2.5KG	04065274082530
413437-25G	04061832081700