16702

(R)-Pantetheine

≥95.0% (HPLC)

• Synonym(s): (2R)-2,4-Dihydroxy-N-[3-[(2-mercaptoethyl)amino]-3-oxopropyl]-3,3-dimethylbutanamide, (R)-2,4-Dihydroxy-N-[2-[(2-mercaptoethyl)carbamoyl]ethyl]-3,3-dimethylbutyramide, (D)-(+)-Pantetheine, N-(Pantothenyl)-β-aminoethanethiol, LBF, Lactobacillus bulgaricus factor
• Empirical Formula (Hill Notation): C₁₁H₂₂N₂O₄S
• CAS Number: 496-65-1
• Molecular Weight: 278.37
• Beilstein: 1714196
• MDL number: MFCD00056757
• UNSPSC Code: 12352205
• PubChem Substance ID: 329751343
• NACRES: NA.79

Properties

• Quality Level: 100
• Assay: ≥95.0% (HPLC)
• form: solid
• optical activity: [α]/D 17±2°, c = 1 in H₂O
• color: white
• storage temp.: −20°C
• SMILES string: OCC(C)(C)[C@@H](O)C(NCCC(NCCS)=O)=O
• InChI: 1S/C11H22N2O4S/c1-11(2,7-14)9(16)10(17)13-4-3-8(15)12-5-6-18/h9,14,16,18H,3-7H2,1-2H3,(H,12,15)(H,13,17)/t9-/m0/s1
• InChI key: ZNXZGRMVNNHPCA-VIFPVBQESA-N

Description

Application

• Structures of carboxylic acid reductase reveal domain dynamics underlying catalysis: This study investigates the structural and dynamic aspects of carboxylic acid reductase enzymes, which are relevant for the conversion processes involving (R)-pantetheine and related compounds (Gahloth et al., 2017).

Biochem/physiol Actions

Metabolite in carbapenem biosynthesis, pantothenate and CoA biosynthesis and biosynthesis of secondary metabolites.

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable