Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

559857

Sigma-Aldrich

2-(2H-Benzotriazol-2-yl)-4-methyl-6-(2-propenyl)phenol

99%

Synonym(s):

2-(3-Allyl-2-hydroxy-5-methylphenyl)-2H-benzotriazole, 2-Allyl-6-(2H-benzotriazol-2-yl)-p-cresol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C16H15N3O
CAS Number:
2170-39-0
Molecular Weight:
265.31
MDL number:
MFCD00236141
UNSPSC Code:
12162002
PubChem Substance ID:
24879824
NACRES:
NA.23

assay

99%

mp

98-101 °C (lit.)

transition temp

transition temp >270 °C

solubility

H2O: insoluble

density

1.3 g/mL at 25 °C (lit.)

SMILES string

Cc1cc(CC=C)c(O)c(c1)-n2nc3ccccc3n2

InChI

1S/C16H15N3O/c1-3-6-12-9-11(2)10-15(16(12)20)19-17-13-7-4-5-8-14(13)18-19/h3-5,7-10,20H,1,6H2,2H3

InChI key

YKONWVIRECCMQE-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Covalently bondable UV light stabilizer.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCQ0169
MKCN8488
MKCN8415
MKCG2697
MKCC8583

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

Zhe Lu et al.
Journal of chromatography. A, 1461, 51-58 (2016-07-19)
Analytical methods were developed for the determination of eight substituted diphenylamines (SDPAs) and six benzotriazole UV stabilizers (BZT-UVs) in blood plasma and fish homogenate matrices. Liquid-liquid extraction by methyl tert-butyl ether and denaturation by KOH following silica gel packed column

Articles

Continuous Flow Manufacturing for Monomer Synthesis

The manufacture of monomers for use in ophthalmic applications is driven by the need for higher purity, improved reliability of manufacturing supply, but ultimately by the need for the increased comfort, convenience, and safety of contact lens wearers. Daily wear contact lenses have the potential to fill this need for many customers; however, their widespread use is constrained by higher costs compared to weekly- or monthly-based lenses. New approaches that improve cost structure and result in higher quality raw materials are needed to help make contact lenses more affordable and accelerate growth of the contact lens market.

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