Anodyne

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Panthenol
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Conformer
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Physical properties
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205.25 g/mol [1]
Solubility>30.8 [ug/mL] (The mean of the results at pH 7.4) [1]
-0.9 [1]
Structural Identifiers
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C9H19NO4 [1]
2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutanamide [1]
CC(C)(CO)C(C(=O)NCCCO)O [1]
InChI=1S/C9H19NO4/c1-9(2,6-12)7(13)8(14)10-4-3-5-11/h7,11-13H,3-6H2,1-2H3,(H,10,14) [1]
InChIKeySNPLKNRPJHDVJA-UHFFFAOYSA-N [1]
Toxicity
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Mouse:
- intraperitoneal: 10100 mg/kg

Panthenol

Panthenol (also known as Panthenol, panthenol, Pantothenol, Pantothenyl alcohol, Pantenol, Panthenolum, Panthenol, racemic, Pantenolo, 2,4-Dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutyramide or Purple Toner)

Chemistry

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Panthenol is a racemic mixture of the

Stereoisomers
LevopanthenolGenerated by the Chemistry Development Kit (http://github.com/cdk)
DexpanthenolGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 4678, Panthenol. Accessed August 14, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/4678

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Panthenol. UNII: WV9CM0O67Z. Global Substance Registration System. Accessed August 14, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/WV9CM0O67Z