Drometrizole Chemical Properties

Melting point:

125.5-129.5 °C(lit.)

Boiling point:

bp10 225°

Density 

1.38

vapor pressure 

0Pa at 20℃

refractive index 

1.5600 (estimate)

Flash point:

54°C

storage temp. 

15-25°C

solubility 

DMSO (Slightly), Methanol (Slightly)

form 

Solid

pka

8.15±0.43(Predicted)

color 

Off-White to Pale Yellow

Water Solubility 

173μg/L at 20℃

Merck 

14,3447

Stability:

Hygroscopic

InChIKey

MCPKSFINULVDNX-UHFFFAOYSA-N

LogP

4.2 at 25℃

CAS DataBase Reference

2440-22-4(CAS DataBase Reference)

NIST Chemistry Reference

Phenol, 2-(2H-benzotriazol-2-yl)-4-methyl-(2440-22-4)

EPA Substance Registry System

2-(2H-Benzotriazol-2-yl)-p-cresol (2440-22-4)

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38-53-43

Safety Statements 

22-24/25-36/37

WGK Germany 

1

RTECS 

GO6860000

HS Code 

29339900

Toxicity

LD50 oral in mouse: 6500mg/kg

MSDS

• Language:English Provider:Benazol P
• Language:English Provider:SigmaAldrich

Drometrizole Usage And Synthesis

Characterization

Drometrizole is an ultraviolet light absorber (UVA) of the hydroxyphenyl benzotriazole class, imparting good light stability to a wide variety of polymers.

Applications

Drometrizole provides ultraviolet protection in a wide variety of polymers including styrene homoand copolymers, engineering plastics such as polyesters and acrylic resins, polyvinyl chloride, and other halogen containing polymers and copolymers (e.g. vinylidenes), acetals and cellulose esters. Elastomers, adhesives, polycarbonate blends, polyurethanes, and some cellulose esters and epoxy materials also benefit from the use of Drometrizole.
   

Features/benefits

Drometrizole features a strong absorption of ultraviolet radiation in the 300-400 nm region. It also has a high degree of photostability over long periods of light exposure. The high absorbance combined with photostability and the ability to release absorbed energy in non sensitizing ways make Drometrizole an effective stabilizer against the effects of ultraviolet light.

Guidelines for use

The use levels of Drometrizole range between 0.10% and 0.50%, depending on substrate and performance requirements of the final application. Drometrizole can be used alone or in a variety of blends and combinations with Ciba IRGAFOS®, Ciba IRGANOX® and Ciba CHIMASSORB® stabilizers where often a synergistic performance is observed. Drometrizole may react with various heavy metal ions to form salts or complexes. For example, if Drometrizole comes into contact with iron or cobalt ions, colored complexes are formed. Reducing and oxidizing agents used in polymerization and curing processes have no effect on the stability of Drometrizole.

Physical Properties

Safety

In accordance with good industrial practice, handle with care and avoid unnecessary personal contact. Protect skin. Prevent contamination of the environment. Avoid dust formation and ignition sources.

Chemical Properties

Light yellow powder

Uses

An ultraviolet light absorber for stabilizing plastics and other organic materials against discoloration and deterioration.

Uses

2(2-Hydroxy-5-methylphenyl)benzotriazol is an UV adsorber for use in plastics, cosmetics, dental materials, acrylic materials, dyes, etc.

Uses

Drometrizole is an intermediate reactant in the synthesis of UV light absorbers for polyester fibers.

Definition

Drometrizole is a member of triazoles.

Application

Intermediate reactant in the synthesis of UV light absorbers for polyester fibers
Reactant for synthesis of:
Benzotriazole UV absorbers with a blocked hydroxy group for us in UV curable paint
Maleimide-bound benzotriazole monomer to use for emulsion polymerization
Used in:
Microstereophotolithography and shape memory alloy for fabrication of miniaturized actuators
PVS and wood / PVC composites as a stabilizer
Acrylonitrile-butadiene-styrene as a UV absorber.

Flammability and Explosibility

Not classified

Drometrizole(2440-22-4)Related Product Information

• Diphenylsilanediol
• Cresol
• CHLOROPHOSPHONAZO III
• Methylparaben
• Bensulfuron methyl
• p-Cresol
• Thiophanate-methyl
• 5-Methyl-1H-benzotriazole
• PHENYL VALERATE
• Kresoxim-methyl
• Tolyltriazole
• Chlorodimethylphenylsilane
• 3-Ethylphenol
• 1H-Benzotriazole
• Trimethylphenylammonium chloride
• Methyl acrylate
• Methyltriphenylphosphonium bromide
• Bisoctrizole