- Arbutin
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ImageFile = Arbutin structure.png
ImageSize = 200px
IUPACName = ("2R,3S,4S,5R,6S")-2-Hydroxymethyl-6- (4-hydroxyphenoxy)oxane-3,4,5-triol
OtherNames = Arbutoside
Hydroquinone β-D-glucopyranoside
Section1 = Chembox Identifiers
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CASNo = 497-76-7
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PubChem = 440936
SMILES = C1=CC(=CC=C1O)O [C@H] 2 [C@@H] ( [C@H] ( [C@@H] ( [C@H] (O2)CO)O)O)O
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Section2 = Chembox Properties
Formula = C12H16O7
MolarMass = 272.251 g/mol
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MeltingPtC = 199.5
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Section7 = Chembox Hazards
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PEL =Arbutin is both an
ether and aglycoside ; a glycosylated benzoquinone extracted frombearberry plant in the genus "Arctostaphylos". It inhibitstyrosinase and thus prevents the formation ofmelanin . Arbutin is therefore used as a skin-lightening agent. Arbutin is also found inwheat , and is concentrated inpear skins.Risks
Arbutin is glucosylated
hydroquinone , [cite journal | quotes = "The potential toxicity of HQ (hydroquinone) is dependent on the route of exposure" | author = O'Donoghue, J L | date = | year = 2006 | month = Sep | title = Hydroquinone and its analogues in dermatology – a risk-benefit viewpoint | journal = Journal of Cosmetic Dermatology | volume = 5 | issue = 3 | pages = 196–203 | doi = 10.1111/j.1473-2165.2006.00253.x
pmid = 17177740 | url = | format = | accessdate = ] and may carry similar cancer risks, [smartskincare.com [http://www.smartskincare.com/conditions/pigmentation/hyperpigmentation-treatments.html Treatment of hyperpigmentation problems / skin lightening] ] although there are also claims that arbutin reduces cancer risk. [Bowman, Lee. July 25, 2005. Scripps Howard News Service. [http://www.knoxstudio.com/shns/story.cfm?pk=BITTERS-07-25-05&cat=AN High yuck factor not necessarily good for us anymore] ] The German Institute of Food Research inPotsdam found that intestinal bacteria can transform arbutin into hydroquinone, which creates an environment favourable forintestinal cancer . It is known that the body excretes 64-75% of arbutin in urine, and arbutin converted to hydroquinone has an antibacterial effect in theurinary tract , hence the use of bearberry inherbal medicine , but it is not known why this substance plays a role in cancer development.References
External links
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