Sinapicacid NEW
Price | Get Latest Price | ||
Package | 1kg | 25kg | 100kg |
Min. Order: | 1kg |
Supply Ability: | 5000kg |
Update Time: | 2024-12-25 |
Product Details
Product Name: Sinapicacid | CAS No.: 530-59-6 |
EC-No.: 208-487-3 | Min. Order: 1kg |
Purity: 98% | Supply Ability: 5000kg |
Release date: 2024/12/25 |
Sinapic acid is a naturally occurring hydroxycinnamic acid, a type of phenolic acid, found in various plants. It belongs to the family of compounds known as phenylpropanoids, which are derived from the amino acid phenylalanine. Sinapic acid is widely distributed in nature and can be found in a variety of fruits, vegetables, cereals, and seeds, particularly in the seeds of mustard, rapeseed, and other Brassica species.
Chemical Structure and Properties
Chemical Formula: C11H12O5
Molecular Weight: 224.21 g/mol
Structure: The chemical structure of sinapic acid includes a benzene ring substituted with a methoxy group (-OCH3) and a hydroxyl group (-OH) at the 3rd and 5th positions, and an acrylic acid side chain (-CH=CH-COOH).
Appearance: Sinapic acid is usually a yellowish crystalline powder.
Solubility: Soluble in organic solvents like ethanol, methanol, and dimethyl sulfoxide (DMSO); slightly soluble in water.
Stability: Stable under normal conditions but should be stored away from light and moisture to prevent degradation.
Applications of Sinapic Acid
1. Antioxidant
Application: Sinapic acid is recognized for its antioxidant properties, which help neutralize free radicals and reduce oxidative stress.
Benefits:
Skin Care: Used in cosmetic formulations for its ability to protect the skin from environmental damage and to slow the aging process.
Food Industry: Added to foods as a natural preservative to extend shelf life and prevent rancidity.
2. Anti-inflammatory
Application: Sinapic acid exhibits anti-inflammatory properties, making it a potential component in pharmaceuticals and nutraceuticals aimed at reducing inflammation.
Benefits:
Therapeutic Use: Investigated for use in the treatment of inflammatory conditions such as arthritis.
3. Neuroprotective Agent
Application: Studies suggest that sinapic acid may have neuroprotective effects, making it a compound of interest in the research of neurodegenerative diseases like Alzheimer's and Parkinson's.
Benefits:
Brain Health: Potential to protect neurons from oxidative damage, which is a common feature in neurodegenerative disorders.
4. Antimicrobial Activity
Application: Sinapic acid has shown antimicrobial properties against a range of bacteria and fungi.
Benefits:
Preservative: Can be used as a natural antimicrobial agent in food and cosmetic products to inhibit the growth of harmful microorganisms.
5. Cancer Research
Application: Sinapic acid is being studied for its potential anticancer properties, particularly in inhibiting the growth and proliferation of cancer cells.
Benefits:
Cancer Prevention: May help reduce the risk of cancer development due to its antioxidant and anti-inflammatory effects.
Safety and Handling
Toxicity: Sinapic acid is generally considered safe when used in appropriate amounts, especially in food and cosmetic products. However, high doses or prolonged use may require further evaluation for safety.
Handling: Standard precautions should be taken when handling sinapic acid in a laboratory or industrial setting, including the use of gloves, eye protection, and appropriate ventilation.
Storage: Should be stored in a cool, dry place, away from direct sunlight and moisture to maintain its stability.
Summary
Sinapic acid is a versatile phenolic compound with significant antioxidant, anti-inflammatory, neuroprotective, antimicrobial, and potential anticancer properties. It is widely used in the food, cosmetic, and pharmaceutical industries due to these beneficial effects. Its natural origin and broad range of applications make it a valuable component in various products aimed at promoting health and well-being.
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Export sales: Ishara Zhang
Skype:Fortunachem201303
E-mail:hk@fortunachem.com
Tel:+86-27-59207851
Whatsapp/Wechat:+8618007136271
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- Since: 2006-04-03
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