Calcium pantothenate USP

Supplier: MP Biomedicals

Synonyms: D-Calcium pantothenateCalcium D-PantothenateD-Pantothenic acid calcium saltCalcium D-(+)-pantothenateCalcium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoateVitamin B5 calcium salt

ICNA0210122805EA 242 EUR
ICNA0210122805
Calcium pantothenate USP
Calcium pantothenate

D-Pantothenic acid is an essential vitamin (except in horses, ruminants). Pantothenic acid is involved in a number of biological reactions including: A precursor in the biosynthesis of coenzyme A, production of energy, catabolism of fatty acids and amino acids, synthesis of fatty acids, phospholipids, sphingolipids, cholesterol and steroid hormones, synthesis of heme and the neurotransmitter acetylcholine and involved in regulation of gene expression and in signal transduction.


  • Presentation: White Crystalline Powder
  • pH: 5% aqueous solution is 7,2 - 8,0 (Lit.)


The principal biologically active forms of pantothenic acid are coenzyme A (CoA) and acyl carrier protein (ACP). In both CoA and ACP, the business center of the molecule is the pantothenic acid metabolite 4'-phosphopantetheine. Coenzyme A is comprised of 4'-phosphopantetheine linked by an anhydride bond to the nucloetide adenosine 5'-monophosphate. 4'-Phosphopantetheine itself is comprised of pantothenic acid linked at one end, via an amide bond, to beta-mercaptoethylamine, derived from L-cysteine, and at the other end to a phosphate group. The sulfhydryl group of 4'-phosphopantetheine, which is the business end of the coenzyme, forms thioesters with acyl groups producing acyl-CoA derivatives, including acetyl-CoA.


D-Pantothenic acid is a precursor in the biosynthesis of coenzyme A . Pantothenol which is a pantotheic acid derivative is used as an ointment that can help cure the ulceration. It has also been shown to improve the lipid profile in the blood and liver. Pantothenic acid has found to have an effect on wound healing. Pantothenic acid and its derivatives, 4'-phosphopantothenic acid, pantothenol and pantethine, have been shown, in vitro, to protect cells against lipid peroxidation. This protective effect is thought to be due to its stimulation of increased cellular levels of coenzyme A. It has also been shown to increase levels of cellular reduced glutathione.


Soluble in water (1 g/2,8 ml; pH of a 5% aqueous solution is 7,2 - 8,0; CO₂-free water: 8,7), glycerol; slightly soluble in ethanol or acetone.

Formula: C₁₈H₃₂CaN₂O₁₀
MW: 476,54 g/mol
Melting Pt: 170…172 °C (lit.)
Storage Temperature: Ambient
MDL Number: MFCD00002766
CAS Number: 137-08-6

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Specification Test Results

Identity Test A Positive
Identity Test B Positive
Alkalinity Passes
Specific Rotation (c=5, water) +25.0 to + 27.5°
Loss on Drying ≤5.0%
Heavy Metals ≤0.002%
Calcium Content (dry basis) 8.2 - 8.6%
Nitrogen Content (dry basis) 5.7 - 6.0%
Ordinary Impurities ≤1.0%
Assay 98%-101%
Total Plate Count 1000 cfu/g
Yeast & Mold 100 cfu/g

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