Online Database of Chemicals from Around the World

4-tert-Butylbenzoic acid
[CAS# 98-73-7]

Top Active Suppliers
Shanghai Worldyang Chemical Co., Ltd. China Inquire  
+86 13651600618
+86 (21) 5679-5779
sales7777@worldyachem.com
QQ chat
WeChat: 13651600618
WhatsApp: +86 13651600618
Chemical manufacturer since 2012
chemBlink premium supplier since 2023
down More Suppliers...
Identification
Classification Chemical reagent >> Organic reagent >> Aromatic acid
Name 4-tert-Butylbenzoic acid
Synonyms PTBBA
Molecular Structure CAS # 98-73-7, 4-tert-Butylbenzoic acid, PTBBA
Molecular Formula C11H14O2
Molecular Weight 178.23
CAS Registry Number 98-73-7
EC Number 202-696-3
SMILES CC(C)(C)C1=CC=C(C=C1)C(=O)O
Properties
Water solubility 0.07 g/L (20 ºC)
Density 1.1±0.1 g/cm3, Calc.*
Melting point 162-165 ºC
Index of Refraction 1.524, Calc.*
Boiling Point 283.3±19.0 ºC (760 mmHg), Calc.*, 280 ºC
Flash Point 134.9±16.2 ºC, Calc.*, 158 ºC
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol symbol   GHS07;GHS08;GHS09 Danger    Details
Hazard Statements H302-H360-H360F-H361-H372-H373-H411    Details
Precautionary Statements P203-P260-P264-P270-P273-P280-P301+P317-P318-P319-P330-P391-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Specific target organ toxicity - repeated exposureSTOT RE1H372
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Reproductive toxicityRepr.1BH360
Reproductive toxicityRepr.1BH360F
Reproductive toxicityRepr.2H361
Specific target organ toxicity - repeated exposureSTOT RE2H373
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.3H311
Acute toxicityAcute Tox.4H312
Reproductive toxicityRepr.1AH360
Acute toxicityAcute Tox.2H330
Specific target organ toxicity - single exposureSTOT SE1H370
Chronic hazardous to the aquatic environmentAquatic Chronic3H411
Eye irritationEye Irrit.2H319
Reproductive toxicityRepr.1BH360F
Transport Information UN 2811
SDS Available
up Discovory and Applicatios
4-tert-Butylbenzoic acid is an aromatic carboxylic acid that belongs to the family of benzoic acids. It is characterized by a tert-butyl group attached to the para position of the benzoic acid structure, giving it unique properties that have made it a subject of interest in various fields. The discovery of 4-tert-butylbenzoic acid dates back to the early 20th century when scientists were exploring the chemical properties and potential applications of substituted benzoic acids. Its synthesis typically involves the alkylation of benzoic acid with tert-butyl halides, a method that allows for the efficient introduction of the bulky tert-butyl group.

One of the primary applications of 4-tert-butylbenzoic acid is in the field of organic synthesis, where it serves as an intermediate in the production of various chemical compounds. It is widely utilized in the synthesis of pharmaceuticals, agrochemicals, and other organic materials due to its ability to undergo various chemical reactions, including esterification and amidation. This versatility makes it an essential building block in the development of more complex molecules.

In the realm of materials science, 4-tert-butylbenzoic acid is employed as a stabilizer for polymers. Its presence can improve the thermal stability of polymers, making them suitable for applications that require materials to withstand high temperatures. This property is particularly beneficial in the production of high-performance plastics and elastomers, where thermal degradation can significantly affect the material's integrity and performance.

Another notable application of 4-tert-butylbenzoic acid is in the cosmetics industry. Due to its mildness and compatibility with various formulations, it is often used as a pH adjuster and stabilizer in cosmetic products. Its inclusion helps maintain the stability and efficacy of active ingredients, contributing to the overall performance of skin care and cosmetic formulations.

The safety of 4-tert-butylbenzoic acid has been a point of consideration in its application. While it is generally regarded as safe for use in various industries, regulatory assessments have been conducted to ensure that it does not pose significant health risks when used in appropriate concentrations. Manufacturers are advised to adhere to established safety guidelines to minimize any potential adverse effects.

Recent studies have begun to explore the potential of 4-tert-butylbenzoic acid in novel applications, including its use in drug delivery systems and as a precursor for functional materials. Researchers are investigating its efficacy in enhancing the bioavailability of certain drugs and its role in the development of advanced materials with specific functional properties.

In summary, 4-tert-butylbenzoic acid is a valuable compound with diverse applications in organic synthesis, materials science, and cosmetics. Its unique properties derived from the tert-butyl substituent contribute to its versatility and effectiveness in various formulations. As research continues to uncover new applications, 4-tert-butylbenzoic acid is poised to remain a significant player in the chemical industry.

References

2022. Aerobic Photooxidation of Toluene Derivatives into Carboxylic Acids with Bromine-Water under Catalyst-Free Conditions. Synlett, 33(12).
DOI: 10.1055/a-1887-7885

2020. Discovery of Novel Peptidomimetic Boronate ClpP Inhibitors with Noncanonical Enzyme Mechanism as Potent Virulence Blockers in Vitro and in Vivo. Journal of Medicinal Chemistry, 63(3).
DOI: 10.1021/acs.jmedchem.9b01746

2022. Towards the mechanism of spermatotoxicity of p-tert-butyl-alpha-methylhydrocinnamic aldehyde: inhibition of late stage ex-vivo spermatogenesis in rat seminiferous tubule cultures by para-tert-butyl- benzoic acid. Archives of Toxicology, 96(10).
DOI: 10.1007/s00204-022-03379-y
Market Analysis Reports
List of Reports Available for 4-tert-Butylbenzoic acid
Related Products
4-(tert-Butyl)benzene-1,2-diamine  4-tert-Butylbenzenesulfonamide  4-Tert-butylbenzenesulfonic acid  4-tert-Butylbenzenesulfonyl chloride  3-tert-Butylbenzenesulphonyl chloride  4-tert-Butylbenzhydrazide  tert-Butyl 1-benzhydryl-3-azetidinylcarbamate  2-tert-Butyl-1H-benzimidazole  tert-Butyl 4-(1H-benzimidazol-2-yl)piperidine-1-carboxylate  3-tert-Butylbenzoic acid  3-tert-Butylbenzonitrile  4-tert-Butylbenzonitrile  2-tert-Butyl-1,4-benzoquinone  N-tert-Butyl-2-benzothiazolesulfenamide  5-tert-Butylbenzo[b]thiophene  4-tert-Butylbenzoylacetonitrile  4-tert-butylbenzoyl Fluoride  1-[3-(4-tert-Butylbenzoyl)propyl]-4-hydroxypiperidine  4-tert-Butylbenzyl alcohol  4-tert-Butylbenzylamine