2-Methyl-4-(2-methylbenzoylamino)benzoic acid

98%

Reagent Code: #208372
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CAS Number 317374-08-6

science Other reagents with same CAS 317374-08-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.295 g/mol
Formula C₁₆H₁₅NO₃
badge Registry Numbers
MDL Number MFCD16038736
thermostat Physical Properties
Boiling Point 382.9±42.0℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.3±0.1g/ml
Storage Room temperature, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of UV absorbers for cosmetic and sunscreen formulations. It contributes to the stabilization of products exposed to sunlight by helping prevent degradation of active ingredients and extending product shelf life. Also utilized in the development of certain pharmaceutical compounds due to its aromatic and functional group arrangement, supporting research in anti-inflammatory agents. Its derivatives are explored for use in polymer stabilization, protecting materials from UV-induced damage in coatings and plastics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,050.00
inventory 5g
10-20 days ฿3,480.00
2-Methyl-4-(2-methylbenzoylamino)benzoic acid
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Used primarily as an intermediate in the synthesis of UV absorbers for cosmetic and sunscreen formulations. It contributes to the stabilization of products exposed to sunlight by helping prevent degradation of active ingredients and extending product shelf life. Also utilized in the development of certain pharmaceutical compounds due to its aromatic and functional group arrangement, supporting research in anti-inflammatory agents. Its derivatives are explored for use in polymer stabilization, protecting

Used primarily as an intermediate in the synthesis of UV absorbers for cosmetic and sunscreen formulations. It contributes to the stabilization of products exposed to sunlight by helping prevent degradation of active ingredients and extending product shelf life. Also utilized in the development of certain pharmaceutical compounds due to its aromatic and functional group arrangement, supporting research in anti-inflammatory agents. Its derivatives are explored for use in polymer stabilization, protecting materials from UV-induced damage in coatings and plastics.

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