Skip to Content
Merck
All Photos(2)

Key Documents

295787

Sigma-Aldrich

DL-Panthenol

99%

Synonym(s):

(±)-α,γ-Dihydroxy-N-(3-hydroxypropyl)-β,β-dimethylbutyramide, (±)-2,4-Dihydroxy-3,3-dimethylbutyric 3-hydroxypropylamide, DL-Pantothenyl alcohol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
HOCH2C(CH3)2CH(OH)CONH(CH2)3OH
CAS Number:
Molecular Weight:
205.25
Beilstein:
1724945
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

solid

mp

66-69 °C (lit.)

functional group

amide
hydroxyl

SMILES string

CC(C)(CO)C(O)C(=O)NCCCO

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)

InChI key

SNPLKNRPJHDVJA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Panthenol exists in two optically active forms, both of which are used in pharmaceutical preparations.

Application

DL-Panthenol has been used in enantiospecific HPLC separation of pantothenic acid, panthenol and pantolactone enantiomers.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

High performance liquid chromatographic determination of panthenol in bulk, premix, and multivitamin preparations.
H Umagat et al.
Analytical chemistry, 52(8), 1368-1370 (1980-07-01)
Determination of optical purity by high-performance liquid chromatography on chiral stationary phases: pantothenic acid and related compounds.
Arai T, et al.
Journal of Chromatography A, 474(2), 405-410 (1989)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service