3-Aminobenzoic acid

98%

Reagent Code: #134617
label
Alias m-aminobenzoic acid;3-aminobenzoic acid
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CAS Number 99-05-8

science Other reagents with same CAS 99-05-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.14 g/mol
Formula C₇H₇NO₂
badge Registry Numbers
EC Number 202-724-4
MDL Number MFCD00007795
thermostat Physical Properties
Melting Point 178-180 °C(lit.)
inventory_2 Storage & Handling
Density 1.51 g/cm3
Storage RT

description Product Description

Used in the synthesis of dyes and pharmaceuticals, particularly as an intermediate in the production of local anesthetics like benzocaine and procaine. It also serves in the preparation of UV-absorbing compounds for sunscreens due to its ability to absorb ultraviolet light. In research, it acts as a building block for organic synthesis, especially in creating heterocyclic compounds. Its amphoteric nature makes it useful in developing ionic liquids and functional materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿460.00
inventory 100g
10-20 days ฿1,050.00
inventory 500g
10-20 days ฿3,600.00
inventory 2.5kg
10-20 days ฿16,080.00
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3-Aminobenzoic acid
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Used in the synthesis of dyes and pharmaceuticals, particularly as an intermediate in the production of local anesthetics like benzocaine and procaine. It also serves in the preparation of UV-absorbing compounds for sunscreens due to its ability to absorb ultraviolet light. In research, it acts as a building block for organic synthesis, especially in creating heterocyclic compounds. Its amphoteric nature makes it useful in developing ionic liquids and functional materials.

Used in the synthesis of dyes and pharmaceuticals, particularly as an intermediate in the production of local anesthetics like benzocaine and procaine. It also serves in the preparation of UV-absorbing compounds for sunscreens due to its ability to absorb ultraviolet light. In research, it acts as a building block for organic synthesis, especially in creating heterocyclic compounds. Its amphoteric nature makes it useful in developing ionic liquids and functional materials.

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