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Bisoctrizole

Bisoctrizole is a broad-spectrum UVA/UVB absorber that belongs to the benzotriazole class of compounds. Bisoctrizole absorbs UV light through hydroxyphenyl groups, causing reversible electronic transitions, thereby converting light energy into heat energy, inhibiting UV-induced material or skin damage. Bisoctrizole is highly efficient in capturing UVA (320-400 nm) and some UVB (280-320 nm) radiation. Bisoctrizole delays the photodegradation of materials such as silicones, improving their UV aging resistance or enhancing the photoprotective ability of sunscreen products[1][2].

Product Specifications

CAS Number

[103597-45-1]

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Biochemical Assay Reagents

Type

Reference compound

Related Pathways

Others

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/Bisoctrizole.html

Purity

98.0

Solubility

Acetone : 1 mg/mL (ultrasonic; warming; heat to 60°C) |DMSO : < 1 mg/mL

Smiles

OC1=C(N2N=C3C(C=CC=C3)=N2)C=C(C(C)(C)CC(C)(C)C)C=C1CC4=CC(C(C)(C)CC(C)(C)C)=CC(N5N=C6C(C=CC=C6)=N5)=C4O

Molecular Formula

C41H50N6O2

Molecular Weight

658.87

Precautions

H302, H315, H319, H335

References & Citations

[1]Ahmed WA, et al. Effect of Bisoctrizole on Ultraviolet (UV) Absorption Properties of Silicone and Effect on Surface Roughness-An In Vitro Study. Indian J Dent Res. 2024 Apr 1;35 (2) :211-215.|[2]Ruscinc N, et al. Vaccinium myrtillus L. extract associated with octocrylene, bisoctrizole, and titanium dioxide: in vitro and in vivo tests to evaluate safety and efficacy. J Cosmet Dermatol. 2022 Oct;21 (10) :4765-4774.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

Launched

Available Sizes

Curated Selection

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