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Benzoic acid

About: Benzoic acid is a research topic. Over the lifetime, 11832 publications have been published within this topic receiving 167127 citations. The topic is also known as: Retardex & E210.


Papers
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Journal ArticleDOI
TL;DR: In this article, the preparation of lanthanum hydroxide and manganese oxide nanoparticles is presented, based on a nonaqueous sol-gel process involving the reaction of La(OiPr)3 and KMnO4 with organic solvents such as benzyl alcohol, 2-butanone and a 1:1 vol. mixture thereof.

69 citations

Journal ArticleDOI
01 Aug 2002-Polymer
TL;DR: In this article, copolymers of aniline and ortho/meta-amino benzoic acid were synthesized by chemical polymerization using an inverse emulsion pathway.

69 citations

Reference EntryDOI
Takao Maki, Kazuo Takeda1
15 Jun 2000
TL;DR: The article as discussed by the authors contains sections titled: ==================\/\/\/\/\/\/\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\£££$££ £££€££/$££ $££•££19.
Abstract: The article contains sections titled: 1. Introduction 2. Physical Properties 3. Chemical Properties 4. Production 5. Quality Specifications 6. Storage, Transportation and Legal Aspects 7. Uses and Economic Aspects 8. Derivatives of Benzoic Acid 8.1. Salts of Benzoic Acid 8.2. Esters of Benzoic Acid 8.3. Benzoyl Chloride 8.4. Benzonitrile 8.5. Alkyl and Acyl Analogues 8.6. Chlorobenzoic Acids 8.7. Aminobenzoic Acids 8.8. Nitrobenzoic Acids 8.9. 3-Sulfobenzoic Acid 8.10. Hexahydrobenzoic Acid 9. Toxicology

69 citations

Journal Article
TL;DR: The binding of a series of simple derivatives of benzoic acid to bovine serum albumin has been investigated, finding the binding appears to be predominantly to the epsilon-amino and possibly the guanidino groups of the protein molecule.
Abstract: The binding of a series of simple derivatives of benzoic acid to bovine serum albumin has been investigated. Drugs such as salicylic acid and γ-resorcylic acid exhibit extensive binding, while p -aminosalicylate, gentisate, p -aminobenzoate, salicylamide and acetylsalicylate show little or no interaction. The carboxylic acid group confers the primary binding capacity upon the compounds, but the presence of ortho hydrogen donors or of alkyl substitution may enhance this capacity. Hydrogen donors in the meta or para position decrease binding. Most of the compounds exhibit two types of binding sites, one of relatively high affinity but small in number, a second of low affinity but in greater number. The former appears to be more structure specific. The nature of the binding sites upon the protein has been investigated by the use of changes in hydrogen ion concentration, and of chemically modified proteins. The binding appears to be predominantly to the epsilon-amino and possibly the guanidino groups of the protein molecule.

69 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023207
2022519
2021217
2020279
2019315
2018332