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D-Pantothenic acid hemicalcium salt_Molecular_structure_CAS_137-08-6)
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D-Pantothenic acid hemicalcium salt

Catalog No. P2250 Name Sigma Aldrich
CAS Number 137-08-6 Website http://www.sigmaaldrich.com
M. F. C18H32CaN2O10 Telephone 1-800-521-8956
M. W. 476.53208 Fax
Purity ≥98% (TLC) Email
Storage Chembase ID: 130810

SYNONYMS

Title
D-泛酸 半钙盐
IUPAC name
({3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoyl}oxy)calcio 3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoate
IUPAC Traditional name
({3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoyl}oxy)calcio 3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoate
Synonyms
维生素 B5
(R)-(+)-N-(2,4-二羟基-3,3-二甲基-1-氧代丁基)-β-丙氨酸 半钙盐
D-泛酸钙

DATABASE IDS

CAS Number 137-08-6
Beilstein Number 3769272
PubChem SID 24898300
MDL Number MFCD00002766
EC Number 205-278-9

PROPERTIES

Purity ≥98% (TLC)
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
RTECS RU4375000
Storage Temperature 2-8°C
German water hazard class 1

DETAILS

Description (简体中文)
Application
生物合成辅酶 A 的前体。
包装
5, 25, 100, 500 g in poly bottle
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
由于游离酸具有不稳定性和吸湿性,因此采用钙盐的形式。
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. P2250.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

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