ETHYL 3-AMINO-4-HYDROXYBENZOATE

≥97%

Reagent Code: #183475
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CAS Number 13052-92-1

science Other reagents with same CAS 13052-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.18854 g/mol
Formula C₉H₁₁NO₃
badge Registry Numbers
MDL Number MFCD09961411
thermostat Physical Properties
Boiling Point 336.7±27.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.253±0.06 g/cm3(Predicted)
Storage 2-8℃, inert gas, avoiding light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and anti-inflammatory agents. It serves as a building block in organic synthesis due to the presence of both amino and hydroxyl functional groups, allowing for multiple modification pathways. Also employed in the development of dyes and UV-absorbing compounds for use in cosmetics and sunscreens. Its ester group facilitates incorporation into larger molecules through coupling reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,350.00
inventory 1g
10-20 days ฿3,390.00
inventory 5g
10-20 days ฿13,360.00
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ETHYL 3-AMINO-4-HYDROXYBENZOATE
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and anti-inflammatory agents. It serves as a building block in organic synthesis due to the presence of both amino and hydroxyl functional groups, allowing for multiple modification pathways. Also employed in the development of dyes and UV-absorbing compounds for use in cosmetics and sunscreens. Its ester group facilitates incorporation into larger molecules through coupling reactions.
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and anti-inflammatory agents. It serves as a building block in organic synthesis due to the presence of both amino and hydroxyl functional groups, allowing for multiple modification pathways. Also employed in the development of dyes and UV-absorbing compounds for use in cosmetics and sunscreens. Its ester group facilitates incorporation into larger molecules through coupling reactions.
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