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Catalog Number:
03979
CAS Number:
135592-13-1
Boc-S-trityl-L-penicillamine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-Pen(Trt)-OH, Boc-β,β-dimethyl-L-Cys(Trt)-OH
Documents
$188.28 /1G
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Product Information

Boc-S-trityl-L-penicillamine is a versatile compound widely utilized in the fields of medicinal chemistry and biochemistry. This compound, known for its unique protective Boc (tert-butyloxycarbonyl) group and trityl moiety, serves as a crucial building block in the synthesis of peptide-based therapeutics and other bioactive molecules. Its ability to selectively protect amino groups while maintaining stability under various reaction conditions makes it an invaluable tool for researchers aiming to develop novel pharmaceuticals.

In addition to its role in peptide synthesis, Boc-S-trityl-L-penicillamine has shown potential in the development of metal-binding agents, particularly in the context of chelation therapy for heavy metal detoxification. Its structural features allow for effective coordination with metal ions, enhancing its applicability in environmental and health-related research. Researchers and industry professionals can leverage this compound's unique properties to streamline their synthesis processes and improve the efficacy of their therapeutic candidates.

Synonyms
Boc-L-Pen(Trt)-OH, Boc-β,β-dimethyl-L-Cys(Trt)-OH
CAS Number
135592-13-1
Purity
≥ 99% (HPLC)
Molecular Formula
C29H33NO4S
Molecular Weight
491.6
MDL Number
MFCD00237381
PubChem ID
19807089
Melting Point
83 - 87 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 46 ± 2 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Pen(Trt)-OH, Boc-β,β-dimethyl-L-Cys(Trt)-OH
CAS Number
135592-13-1
Purity
≥ 99% (HPLC)
Molecular Formula
C29H33NO4S
Molecular Weight
491.6
MDL Number
MFCD00237381
PubChem ID
19807089
Melting Point
83 - 87 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 46 ± 2 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-S-trityl-L-penicillamine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and enhancing the yield of desired products.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals, particularly in designing drugs that target specific biological pathways, improving efficacy and reducing side effects.
  • Bioconjugation: The compound is employed in bioconjugation processes, facilitating the attachment of biomolecules to drugs or imaging agents, which is essential in targeted therapies.
  • Research in Medicinal Chemistry: Its unique properties make it valuable in medicinal chemistry research, where it aids in the exploration of new therapeutic agents and their mechanisms of action.
  • Analytical Chemistry: Boc-S-trityl-L-penicillamine is used in analytical applications for the detection and quantification of various biomolecules, enhancing the accuracy of biochemical assays.

Citations