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  • 84380-01-8, alpha-熊果苷, a-Arbutin, CAS:84380-01-8
84380-01-8, alpha-熊果苷, a-Arbutin, CAS:84380-01-8

84380-01-8, alpha-熊果苷, a-Arbutin, CAS:84380-01-8

84380-01-8, alpha-熊果苷,
a-Arbutin,
CAS:84380-01-8
MFCD09838262
C12H16O7 / 272.25

alpha-熊果苷,a-Arbutin

Arbutin or alpha-arbutin is a natural product. It is a hydroquinone glucoside with antioxidant properties. It is widely used in cosmetics as depigmenting agent, acting as an inhibitor of tyrosinase in melanocytes. Arbutin acts by supressing the enzymes that stimulate these melanocytes without killing or fully inhibiting them. As a consequence, melanin production is decreased to avoid hyperpigmentation that might be caused by an excess of UV radiation or a higher activity of tyrosinases.

Alpha-Arbutin is a chemical compound that is derived from hydroquinone. It is widely used in various fields of research and the beauty industry due to its potent inhibitory effects on the production of melanin in the skin. In this paper, we will discuss the definition, physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions of alpha-arbutin.

Definition and Background:

Alpha-Arbutin (4-hydroxyphenyl-alpha-D-glucopyranoside) is a naturally occurring glycosylated hydroquinone. It is derived from the leaves of berries such as the bearberry, cranberry, and blueberry. Alpha-Arbutin has been widely used in the beauty industry due to its skin lightening and anti-aging properties. It is also used in food and cosmetic products as a preservative and stabilizer.

Synthesis and Characterization:

Alpha-Arbutin can be synthesized by the reaction of hydroquinone with alpha-D-glucose. The reaction produces alpha-arbutin and water. The synthesis of alpha-arbutin is a relatively simple process that can be carried out in a laboratory or industrial setting. The compound can be characterized using various techniques such as nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and mass spectrometry (MS).

Analytical Methods:

Alpha-Arbutin can be analyzed using various analytical methods such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS). HPLC is a widely used analytical method that is used to separate and quantify the components of a mixture. GC-MS is another technique that is used to identify the individual components of a mixture.

Biological Properties:

Alpha-Arbutin has been shown to inhibit the production of melanin in the skin. Melanin is the pigment that gives skin its color. Alpha-Arbutin works by inhibiting the enzyme that produces melanin. This has led to its use in the beauty industry as a skin lightening agent. Alpha-Arbutin has also been shown to have antioxidant properties that can protect the skin from damage caused by free radicals.

Toxicity and Safety in Scientific Experiments:

Alpha-Arbutin has been shown to be safe and non-toxic in scientific experiments. However, more research is needed to determine its safety in a clinical setting. Alpha-Arbutin should not be ingested and should only be used topically.

Applications in Scientific Experiments:

Alpha-Arbutin has been used in various scientific experiments. It has been used in studies investigating the effects of melanin on skin pigmentation, as well as the effects of antioxidants on skin aging. Alpha-Arbutin has also been used as a preservative in food products.

Current State of Research:

The current state of research on alpha-arbutin is promising. Studies have shown its efficacy as a skin lightening agent and as an antioxidant. However, more research is needed to fully understand its mechanisms of action and potential uses.

Potential Implications in Various Fields of Research and Industry:

Alpha-Arbutin has potential implications in various fields of research and industry. It has been widely used in the beauty industry as a skin lightening agent and anti-aging compound. It also has potential uses in the food industry as a preservative and stabilizer. In addition, alpha-arbutin has potential uses in scientific research investigating the effects of melanin on skin pigmentation and aging.

Limitations and Future Directions:

One limitation of alpha-arbutin is its stability. It is prone to oxidation, which can decrease its efficacy over time. Future research should investigate ways to increase the stability of alpha-arbutin, as well as its efficacy as a skin lightening agent and antioxidant. Additionally, more research is needed to fully understand its safety and potential uses in a clinical setting.

Future Directions:

1. Investigation of the efficacy of alpha-arbutin as a skin lightening agent in clinical trials.

2. Determination of the optimal concentration of alpha-arbutin in cosmetic and beauty products.

3. Investigation of the potential uses of alpha-arbutin in wound healing and tissue repair.

4. Development of new and innovative formulations of alpha-arbutin to increase its efficacy and stability.

5. Investigation of the potential uses of alpha-arbutin in the treatment of skin diseases such as vitiligo.

6. Examination of the effect of alpha-arbutin on other types of pigmentation disorders such as age spots.

7. Exploration of the potential uses of alpha-arbutin in the treatment of certain types of cancer.

8. Investigation of the safety and efficacy of alpha-arbutin in children and pregnant women.

9. Development of new analytical methods for the quantification of alpha-arbutin in cosmetic and food products.

10. Exploration of the potential uses of alpha-arbutin in the development of new drug therapies.

CAS Number84380-01-8
Product Namealpha-Arbutin
IUPAC Name(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol
Molecular FormulaC12H16O7
Molecular Weight272.25 g/mol
InChIInChI=1S/C12H16O7/c13-5-8-9(15)10(16)11(17)12(19-8)18-7-3-1-6(14)2-4-7/h1-4,8-17H,5H2/t8-,9-,10+,11-,12+/m1/s1
InChI KeyBJRNKVDFDLYUGJ-ZIQFBCGOSA-N
Synonyms4-Hydroxyphenyl-α-D-glucopyranoside; Hydroquinone O-α-D-Glucopyranoside;
Canonical SMILESC1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O
Isomeric SMILESC1=CC(=CC=C1O)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O


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