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Merck
CN

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

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About This Item

Empirical Formula (Hill Notation):
C11H22N2O4S
CAS Number:
496-65-1
Molecular Weight:
278.37
UNSPSC Code:
12352205
NACRES:
NA.79
PubChem Substance ID:
329751343
MDL number:
MFCD00056757
Beilstein/REAXYS Number:
1714196

Key Documents

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InChI key

ZNXZGRMVNNHPCA-VIFPVBQESA-N

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

assay

≥95.0% (HPLC)

form

solid

optical activity

[α]/D 17±2°, c = 1 in H2O

color

white

storage temp.

−20°C

Quality Level

100

Related Categories

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.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB7634
BCBZ9006
BCBM8211V
BCBM8211

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