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Classification | Biochemical >> Plant extracts |
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Name | alpha-Arbutin |
Synonyms | 4-Hydroquinone-alpha-D-glucopyranoside |
Molecular Structure | ![]() |
Molecular Formula | C12H16O7 |
Molecular Weight | 272.25 |
CAS Registry Number | 84380-01-8 |
EC Number | 440-470-8 |
SMILES | C1=CC(=CC=C1O)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O |
Density | 1.6±0.1 g/cm3, Calc.* |
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Melting point | 195-196 ºC |
Index of Refraction | 1.650, Calc.* |
Boiling Point | 561.6±50.0 ºC (760 mmHg), Calc.* |
Flash Point | 293.4±30.1 ºC, Calc.* |
* | Calculated using Advanced Chemistry Development (ACD/Labs) Software. |
Hazard Symbols |
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Hazard Statements | H302 Details | ||||||||||||
Precautionary Statements | P264-P270-P301+P317-P330-P501 Details | ||||||||||||
Hazard Classification | |||||||||||||
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SDS | Available | ||||||||||||
Alpha-arbutin is a naturally occurring glycoside and a derivative of hydroquinone, predominantly found in various plant sources, including bearberry, blueberry, and cranberry. Its discovery can be traced back to the mid-20th century when researchers explored the glycosylation of hydroquinone to create safer and more stable compounds for cosmetic applications. Unlike its parent compound, hydroquinone, which has been associated with potential side effects such as skin irritation and cytotoxicity, alpha-arbutin offers a safer alternative for skin-lightening and depigmenting applications. The chemical structure of alpha-arbutin consists of a hydroquinone moiety linked to a glucose molecule, which contributes to its stability and solubility in water. This structural configuration allows alpha-arbutin to inhibit the activity of tyrosinase, an enzyme critical for melanin production in the skin. By doing so, alpha-arbutin helps to reduce hyperpigmentation, dark spots, and uneven skin tone, making it a popular ingredient in skincare formulations aimed at brightening and evening out the skin. One of the primary applications of alpha-arbutin is in the cosmetic industry, where it is widely used in serums, creams, and lotions designed to improve skin clarity and reduce the appearance of dark spots. Its efficacy as a skin-lightening agent has been supported by various studies, which indicate that alpha-arbutin can achieve noticeable results with regular use. Moreover, its gentle nature makes it suitable for all skin types, including sensitive skin, which is a significant advantage over other harsher skin-lightening agents. In addition to its skin-lightening properties, alpha-arbutin has been investigated for its potential antioxidant effects. This aspect is particularly relevant as antioxidants play a crucial role in protecting the skin from oxidative stress caused by environmental factors, such as UV radiation and pollution. By incorporating alpha-arbutin into formulations, manufacturers can enhance the overall protective effects of their products, offering consumers additional benefits. The safety profile of alpha-arbutin has been a critical factor in its acceptance in the cosmetic market. Regulatory bodies in various countries have recognized its safety for topical use, contributing to its widespread adoption. Unlike hydroquinone, which has faced restrictions in several regions due to safety concerns, alpha-arbutin has emerged as a preferred alternative for both consumers and formulators. Research continues to explore additional applications of alpha-arbutin beyond cosmetic use. Studies have suggested that it may possess anti-inflammatory properties, which could further enhance its appeal in skincare formulations. As interest in natural and safer cosmetic ingredients grows, alpha-arbutin remains a focal point for researchers and manufacturers seeking effective solutions for skin concerns. In summary, alpha-arbutin is a valuable compound in the realm of skincare, recognized for its skin-lightening and antioxidant properties. Its discovery as a safer alternative to hydroquinone has led to its widespread application in various cosmetic products, promoting a brighter and more even complexion. Ongoing research may further unveil its potential, solidifying its place as a key ingredient in modern skincare. References 2018. Recent progress on biological production of α-arbutin. Applied Microbiology and Biotechnology, 102(19). DOI: 10.1007/s00253-018-9241-9 2012. Biotechnological production of arbutins (α- and β-arbutins), skin-lightening agents, and their derivatives. Applied Microbiology and Biotechnology, 95(6). DOI: 10.1007/s00253-012-4297-4 2011. Recovery of arbutin in high purity from fruit peels of pear (Pyrus pyrifolia Nakai). Food Science and Biotechnology, 20(3). DOI: 10.1007/s10068-011-0111-9 |
Market Analysis Reports |
List of Reports Available for alpha-Arbutin |