4-[(Oxan-2-yl)oxy]phenol

HCID 11745519

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Grundinformationen

CAS
53936-56-4
Standard-SMILES
Oc1ccc(OC2CCCCO2)cc1
InChIKey
GFBCWCDNXDKFRH-UHFFFAOYSA-N
Summenformel
C11H14O3
Durchschnittliche Molmasse
194,23 g/mol
Monoisotopische Masse
194,09429431

Namen und Bezeichner

Bevorzugter Name
4-[(Oxan-2-yl)oxy]phenol
IUPAC
4-[(Oxan-2-yl)oxy]phenol
Englischer Name
Deoxyarbutin
Summenformel
C11H14O3
Molmasse
194.23

Namen und Synonyme

TetrahydropyranyloxyphenolDexyarbutinDeoxyarbutinLGB-D ARBUTINDeoxyarbutin, 96%Deoxyarbutin, 98%+4-(oxan-2-yloxy)phenolDeoxyarbutin 53936-56-4Pure Deoxyarbutin PowderDeoxyarbutin, 10 mM in DMSO

Datenbank-Bezeichner

CAS
53936-56-4
PubChem CID
11745519
DTXSID
DTXSID10968728
ChEMBL
CHEMBL4303145
UNII
RG969BY5EN
EC Number
800-360-6
Nikkaji
J1.158.216H

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
88 · 88-89 °C(Solv: ligroine (8032-32-4))
Siedepunkt
349.8 · 349.8±32.0 °C(Predicted)
Dichte
1.174 · 1.174
storage temp.
2 · under inert gas (nitrogen or Argon) at 2-8°C
Löslichkeit
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly, Sonicated)
pka
10.1 · 10.10±0.15(Predicted)

Sicherheit und Regulatorisches

Sicherheitsdaten

hs_code
2932990090

Chemie und Industrie

Anwendungen · 2 Einträge

BeschreibungDeoxyarbutin 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.

VerwendenDeoxyarbutin acts as a skin whitening agent through the inhibition of tyrosinase. A safer alternative to the use of hydroquinone and arbutin.

Darstellung

synthetischeDeoxyarbutin is a derivative of -arbutin, obtained by removal of hydroxyl groups from the glucose side-chain of -arbutin.

Anbieter100 Anbieter

北京华美互利生物化工010-56205725 · [email protected]
郑州阿尔法化工有限公司+86-18530059196 · [email protected]
衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
INTATRADE GmbH+49 3493/605464 · [email protected]
河北创海生物科技有限公司+86-86-13131129325 · [email protected]

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