594695
Fmoc-Asp-OH-2-13C
99 atom % 13C
Synonym(s):
N-(9-Fluorenylmethoxycarbonyl)-L-aspartic-2-13C acid, L-Aspartic-2-13C acid, N-Fmoc dervative
About This Item
isotopic purity
99 atom % 13C
form
solid
technique(s)
bio NMR: suitable
mp
179-181 °C (lit.)
application(s)
peptide synthesis
functional group
Fmoc
mass shift
M+1
storage temp.
2-8°C
SMILES string
OC(=O)C[13C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
InChI
1S/C19H17NO6/c21-17(22)9-16(18(23)24)20-19(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H,20,25)(H,21,22)(H,23,24)/t16-/m0/s1/i16+1
InChI key
KSDTXRUIZMTBNV-JCETWUESSA-N
General description
Application
- Metabolomic profiling and pathway analysis
- Stable Isotope probing in Environmental microbiology
- reaction mechanism investigations
Features and Benefits
- High isotopic purity for reliable synthesis.
- Stable isotopic composition for consistent results.
- Versatile applications across various therapeutic areas.
- Compatibility with multiple diagnostic platforms.
Benefits
- Enhances the accuracy and reliability of metabolic studies.
- Increases efficiency in drug development processes.
- Supports regulatory compliance and safety standards.
- Provides a competitive advantage in the pharmaceutical market.
Packaging
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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