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Deoxyarbutin

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CAS:53936-56-4
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Deoxyarbutin Basic information
Product Name:Deoxyarbutin
Synonyms:Deoxyarbutin;Tetrahydropyranyloxyphenol;4-(TETRAHYDRO-2H-2-PYRANYLOXY)PHENOL;4-[(Tetrahydro-2H-pyran-2-yl)oxy]phenol;Phenol,4-[(tetrahydro-2H-pyran-2-yl)oxy]-;Deoxyarbutin 4-[(Tetrahydro-2H-pyran-2-yl)oxy]phenol;4-[(2-Tetrahydropyranyl)oxy]phenol;LGB-D ARBUTIN
CAS:53936-56-4
MF:C11H14O3
MW:194.23
EINECS:1308068-626-2
Product Categories:Inhibitors;Cosmetics;53936-56-4
Mol File:53936-56-4.mol
Deoxyarbutin Structure
Deoxyarbutin Chemical Properties
Melting point 88-89 °C(Solv: ligroine (8032-32-4))
Boiling point 349.8±32.0 °C(Predicted)
density 1.174
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly, Sonicated)
form Solid
pka10.10±0.15(Predicted)
color White to Off-White
Stability:Hygroscopic
Cosmetics Ingredients FunctionsBLEACHING
InChIInChI=1S/C11H14O3/c12-9-4-6-10(7-5-9)14-11-3-1-2-8-13-11/h4-7,11-12H,1-3,8H2
InChIKeyGFBCWCDNXDKFRH-UHFFFAOYSA-N
SMILESC1(O)=CC=C(OC2OCCCC2)C=C1
Safety Information
HS Code 2932990090
MSDS Information
Deoxyarbutin Usage And Synthesis
DescriptionDeoxyarbutin is a tyrosinase inhibitor (IC50 = 17.5 μM for mushroom tyrosinase). It reduces melanin content in isolated dark human melanocytes when used at a concentration of 1.56 μM. Topical administration of deoxyarbutin (5%) induces skin lightening in human skin mouse xenograft models. Deoxyarbutin also inhibits proliferation of B16/F10 murine melanoma cells (EC50 = 39.56 μM). It induces apoptosis and halts the cell cycle at the S phase in B16/F10 cells when used at a concentration of 50 μM. Deoxyarbutin (50 mg/kg) reduces tumor growth in a B16/F10 murine melanoma model.
UsesDeoxyarbutin acts as a skin whitening agent through the inhibition of tyrosinase. A safer alternative to the use of hydroquinone and arbutin.
PreparationDeoxyarbutin is a derivative of -arbutin, obtained by removal of hydroxyl groups from the glucose side-chain of -arbutin.
Synthesis
3,4-Dihydro-2H-pyran

110-87-2

Hydroquinone

123-31-9

Deoxyarbutin

53936-56-4

Under nitrogen protection, 3,4-dihydro-2H-pyran (19.1 g, 227.0 mmol) was dissolved in a solution of dichloromethane (200 ml) containing pyridinium p-toluenesulfonate (PPTS) (5.7 g, 22.7 mmol). After cooling the reaction system to 10°C, a solution of hydroquinone (25.0 g, 227.0 mmol) in dichloromethane (100 ml) was added slowly and dropwise. Subsequently, the reaction mixture was gradually warmed to 25°C and stirred continuously for 16 hours. After completion of the reaction, the mixture was poured into water (500 ml) and the aqueous layer was extracted with dichloromethane. The organic layers were combined and washed sequentially with saturated aqueous sodium chloride solution and saturated aqueous sodium bicarbonate solution, then dried with anhydrous magnesium sulfate. The organic phase was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (eluent: toluene/ethyl acetate=5:1, v/v) to afford 4-((tetrahydro-2H-pyran-2-yl)oxy)phenol (23.2 g, 119.7 mmol, 52.7% yield).

References[1] Canadian Journal of Chemistry, 2006, vol. 84, # 9, p. 1174 - 1179
[2] Patent: JP5978938, 2016, B2. Location in patent: Paragraph 0149; 0154
[3] Journal of Materials Chemistry, 2012, vol. 22, # 48, p. 25011 - 25018
[4] Patent: US2009/326186, 2009, A1. Location in patent: Page/Page column 64
[5] Angewandte Chemie - International Edition, 2013, vol. 52, # 16, p. 4356 - 4360
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