Substance

ID:180780

D-Pantothenic acid hemicalcium salt

Names and Identifiers
IUPAC Traditional name
({3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoyl}oxy)calcio 3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoate
Synonyms
D-Pantothenic acid hemicalcium saltD-泛酸 半钙盐D-泛酸钙维生素 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
IUPAC name
({3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoyl}oxy)calcio 3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoate
Registration numbers
MDL Number
Beilstein Number
EC Number
CAS Number
PubChem SID
Properties
Product Information
Purity
≥98% (TLC)
Safety Information
Storage Temperature
2-8°C
German water hazard class
1
RTECS
RU4375000
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Molecule Details
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.
Molecular Spectra
No Data Available
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References
No Data Available
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