3-(tert-Butyl)benzoic acid

≥95%

Reagent Code: #148543
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CAS Number 7498-54-6

science Other reagents with same CAS 7498-54-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.23 g/mol
Formula C₁₁H₁₄O₂
badge Registry Numbers
MDL Number MFCD01463861
thermostat Physical Properties
Boiling Point 286°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its bulky tert-butyl group enhances lipophilicity, making it valuable in modifying the solubility and stability of active ingredients. Also employed in the production of specialty polymers and UV stabilizers due to its resistance to degradation under light exposure. Additionally, it serves as a building block in organic synthesis for introducing aromatic carboxylic acid functionality with steric hindrance.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,780.00
inventory 5g
10-20 days ฿8,600.00
inventory 10g
10-20 days ฿18,260.00

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3-(tert-Butyl)benzoic acid
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its bulky tert-butyl group enhances lipophilicity, making it valuable in modifying the solubility and stability of active ingredients. Also employed in the production of specialty polymers and UV stabilizers due to its resistance to degradation under light exposure. Additionally, it serves as a building block in organic synthesis for introducing aromatic carboxylic

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its bulky tert-butyl group enhances lipophilicity, making it valuable in modifying the solubility and stability of active ingredients. Also employed in the production of specialty polymers and UV stabilizers due to its resistance to degradation under light exposure. Additionally, it serves as a building block in organic synthesis for introducing aromatic carboxylic acid functionality with steric hindrance.

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