Hexyl 4-aminobenzoate hydrochloride

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Reagent Code: #131623
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CAS Number 2703752-44-5

science Other reagents with same CAS 2703752-44-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.76 g/mol
Formula C₁₃H₂₀ClNO₂
badge Registry Numbers
MDL Number MFCD34476093
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. It serves as a building block for ester-based local anesthetics, such as benzocaine analogs, contributing to the development of compounds with numbing properties. Its amino and ester functional groups allow for further chemical modifications, making it valuable in research settings for designing new bioactive molecules. Additionally, the compound itself is utilized in some cosmetic formulations as a UVB absorber in sunscreens, providing effective protection against ultraviolet radiation due to its structural properties similar to other p-aminobenzoate esters.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,630.00
inventory 250mg
10-20 days ฿6,040.00
inventory 1g
10-20 days ฿17,640.00

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Hexyl 4-aminobenzoate hydrochloride
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Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. It serves as a building block for ester-based local anesthetics, such as benzocaine analogs, contributing to the development of compounds with numbing properties. Its amino and ester functional groups allow for further chemical modifications, making it valuable in research settings for designing new bioactive molecules. Additionally, the compound itself is utilized in some cosmetic

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. It serves as a building block for ester-based local anesthetics, such as benzocaine analogs, contributing to the development of compounds with numbing properties. Its amino and ester functional groups allow for further chemical modifications, making it valuable in research settings for designing new bioactive molecules. Additionally, the compound itself is utilized in some cosmetic formulations as a UVB absorber in sunscreens, providing effective protection against ultraviolet radiation due to its structural properties similar to other p-aminobenzoate esters.

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