Weight | 205.254 g/mol |
---|---|
Formula | C9H19NO4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 4 |
Aromatic Rings | 0 |
Rotatable Bonds | 6 |
Dexpanthenol (81-13-0)
panthenol · Ilopan · pantothenol
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- Sigma-Aldrich - Dexpanthenol50.20 USD
- Fisher Scientific - Search for Dexpanthenol
- TCI - Search for Dexpanthenol
- Topical Use of Dexpanthenol in Skin Disorders (American Journal of Clinical Dermatology, 2002)
- Effect of topically applied dexpanthenol on epidermal barrier function and stratum corneum hydration results of a human in vivo study (Drug Research, 2011)
- Efficacy of dexpanthenol in skin protection against irritation: a double-blind, placebo-controlled study (Contact Dermatitis, 2003)
- Dexpanthenol enhances skin barrier repair and reduces inflammation after sodium lauryl sulphate-induced irritation (Journal of Dermatological Treatment, 2002)
- Dexpanthenol attenuates lipid peroxidation and testicular damage at experimental ischemia and reperfusion injury (Pediatric Surgery International, 2007)
- Colorimetric Determination of Panthenol and Pantothenates (Analytical Chemistry, 1950)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - panthenol
- Ilopan
- pantothenol
- Panthoderm
- Panthenol Jenapharm
- Panthogenat
- Panthenol-ratiopharm
- Ucee D
- Otriven Dexpanthenol
- butanamide, 2,4-dihydroxy-n-(3-hydroxypropyl)-3,3-dimethyl-, (+--)-
- Repa-Ophtal
- Siozwo SANA
- DL-panthenol
- panthenol von ct
- Panthenol LAW
- Wund- und Heilsalbe LAW
- Bepanthen
- D-panthenol
- Pan Rhinol
- Rhinoclir
- NasenSpray ratiopharm Panthenol
- Nasicur
- Panthenol Lichtenstein
- Panthenol Braun
- Corneregel
- Marolderm
- Urupan
- Pan-Ophtal
- Dexpanthenol Heumann
-
SMILESCC(C)(CO)C(C(=O)NCCCO)O
-
InChIKeySNPLKNRPJHDVJA-UHFFFAOYSA-N
- Pubchem - Dexpanthenol
- Wikipedia - panthenol
Panthenol (also called pantothenol) is the alcohol analog of pantothenic acid (vitamin B5), and is thus a provitamin of B5. In organisms it is quickly oxidized to pantothenic acid. It is a viscous transparent liquid at room temperature.
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Synthesis
3-Hydroxy-2,2-dimethylpropanal
+
Reactant
(Grignard alcohol)
Reactant
+
3-Aminopropanol
(Schotten-Baumann amide from acid)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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