P2250

D-Pantothenic acid hemicalcium salt

≥98% (TLC)

• Synonym(s): (R)-(+)-N-(2,4-Dihydroxy-3,3-dimethyl-1-oxobutyl)-β-alanine hemicalcium salt, Calcium D-pantothenate, Vitamin B₅
• Linear Formula: HOCH₂C(CH₃)₂CH(OH)CONHCH₂CH₂CO₂ ·1/2Ca
• CAS Number: 137-08-6
• Molecular Weight: 238.27
• Beilstein/REAXYS Number: 3769272
• EC Number: 205-278-9
• MDL number: MFCD00002766
• UNSPSC Code: 12352200
• eCl@ss: 34058012
• PubChem Substance ID: 57654509

Properties

• biological source: synthetic (organic)
• assay: ≥98% (TLC)
• form: powder
• color: white to off-white
• storage temp.: 2-8°C
• SMILES string: CC(C)(CO)[C@@H](O)C(=O)NCCC(=O)O[Ca]OC(=O)CCNC(=O)[C@H](O)C(C)(C)CO
• InChI: 1S/2C9H17NO5.Ca/c2*1-9(2,5-11)7(14)8(15)10-4-3-6(12)13;/h2*7,11,14H,3-5H2,1-2H3,(H,10,15)(H,12,13);/q;;+2/p-2/t2*7-;/m00./s1
• InChI key: FAPWYRCQGJNNSJ-UBKPKTQASA-L

Description

Application

Precursor in the biosynthesis of coenzyme A.

Biochem/physiol Actions

D-Panthenol is the alcohol analogue and biological precursor of D-pantothenic acid. These analogues are precursors in the biosynthesis of coenzyme A. D-Panthenol and D-Pantothenic acid are used in a variety of skin protection products. D-pantothenic acid may have a role in controlling keratinocyte proliferation and differentiation. D-Panthenol may be used for studies of skin protection emulsions from UV irradiation and as a humectant.

Physical properties

Due to the unstable, hygroscopic nature of the free acid, the calcium salt is employed.

Safety Information

• Storage Class: 13 - Non Combustible Solids
• wgk_germany: WGK 1
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)