Synonym: (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
CAS Number: 496-65-1
Empirical Formula (Hill Notation): C11H22N2O4S
Molecular Weight: 278.37
MDL Number: MFCD00056757
Linear Formula: C11H22N2O4S
Product Type: Chemical
assay |
≥95.0% (HPLC) |
color |
white |
form |
solid |
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 |
optical activity |
[α]/D 17±2°, c = 1 in H2O |
Quality Level |
100 |
SMILES string |
OCC(C)(C)[C@@H](O)C(NCCC(NCCS)=O)=O |
storage temp. |
−20°C |
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. |
Hazard Codes |
T |
Risk Statements |
25 |
Safety Statements |
45 |
RIDADR |
UN 2811 6.1 / PGIII |
WGK Germany |
WGK 3 |
Flash Point(F) |
Not applicable |
Flash Point(C) |
Not applicable |
Purity |
≥95.0% (HPLC) |
Storage Temp. |
−20°C |
UNSPSC |
12352200 |