100-09-4
100-09-4
Chemical Structure
p-Anisic acid
Synonym(s): 4-Methoxybenzoic acid; Draconic acid
- CAS No.: 100-09-4
- Formula:C8H8O3
- Molecular Weight:152.15
IUPAC Name: 4-methoxybenzoic acid
InChIKey: ZEYHEAKUIGZSGI-UHFFFAOYSA-N
SMILES: O=C(O)C1=CC=C(OC)C=C1
Biological Activity: p-Anisic acid (4-Methoxybenzoic acid) is an orally available tyrosinase inhibitor that has antioxidant, anti-anxiety, anti-inflammatory, anti-tumor, anti-diabetic, and preservative properties. p-Anisic acid can be used as a preservative in the cosmetics field[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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p-Anisic acid | 99.79% | p-Anisic acid (4-Methoxybenzoic acid) is an orally available tyrosinase inhibitor that has antioxidant, anti-anxiety, anti-inflammatory, anti-tumor, anti-diabetic, and preservative properties. p-Anisic acid can be used as a preservative in the cosmetics field. | ||||||||||||||||||||
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p-Anisic acid (Standard) | 99.49% | p-Anisic acid (Standard) is the analytical standard of p-Anisic acid. This product is intended for research and analytical applications. p-Anisic acid (4-Methoxybenzoic acid) is one of the isomers of anisic acid, with anti-bacterial and antiseptic properties. | ||||||||||||||||||||
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p-Anisic acid-d4 | 99.9% | p-Anisic acid-d4 is the deuterium labeled p-Anisic acid. p-Anisic acid (4-Methoxybenzoic acid) is one of the isomers of anisic acid, with anti-bacterial and antiseptic properties. | ||||||||||||||||||||
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p-Anisic acid-13C6 | p-Anisic acid-13C6 is the 13C-labeled p-Anisic acid. p-Anisic acid (4-Methoxybenzoic acid) is one of the isomers of anisic acid, with anti-bacterial and antiseptic properties. | |||||||||||||||||||||
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p-Anisic acid-d7 | p-Anisic acid-d7 (4-Methoxybenzoic acid-d7) is the deuterium labeled p-Anisic acid (HY-N1394). p-Anisic acid (4-Methoxybenzoic acid) is an orally available tyrosinase inhibitor that has antioxidant, anti-anxiety, anti-inflammatory, anti-tumor, anti-diabetic, and preservative properties. p-Anisic acid can be used as a preservative in the cosmetics field. | |||||||||||||||||||||
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References
- [1]. DeWeerd K, et al. Metabolism of the 18O-methoxy substituent of 3-methoxybenzoic acid and other unlabeled methoxybenzoic acids by anaerobic bacteria. Appl Environ Microbiol. 1988 May;54(5):1237-42. [Content Brief]
- [2]. Gandhi P J, et al. Transmission of p-anisic acid through nanofiltration and goat membranes[J]. Desalination, 2013, 315: 46-60.
- [3]. K Nakamura, et al. Anxiolytic effects of aniracetam in three different mouse models of anxiety and the underlying mechanism. Eur J Pharmacol. 2001 May 18;420(1):33-43. [Content Brief]
- [4]. Vishal Vora, et al. Anti-Diabetic and Insulinotropic Effects of p-Anisic Acid in High-Fat Diet and Streptozotocin Induced Type-2 Diabetic Rats. Chem Biodivers. 2024 Aug 29:e202401575. [Content Brief]
