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Catalog Number:
07150
CAS Number:
325708-26-7
Trityl-1,6-diaminohexane acetate salt
Purity:
≥ 99% (HPLC)
Synonym(s):
N-Trityl-1,6-hexanediamine acetate salt
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Product Information

Trityl-1,6-diaminohexane·AcOH is a versatile compound that combines the properties of a trityl group with a diaminohexane backbone, making it an essential building block in various chemical syntheses. This compound is particularly valued in the field of organic chemistry for its ability to serve as a protecting group for amines, facilitating the selective functionalization of complex molecules. Its unique structure allows for enhanced stability and reactivity, which is crucial in the development of pharmaceuticals and agrochemicals. Researchers often utilize Trityl-1,6-diaminohexane·AcOH in peptide synthesis and the preparation of advanced materials, where its protective capabilities can streamline multi-step reactions.

In addition to its synthetic applications, this compound is also explored for its potential in drug development, particularly in the formulation of targeted therapies. The presence of the trityl group enhances solubility and bioavailability, making it a candidate for further investigation in medicinal chemistry. With its robust profile, Trityl-1,6-diaminohexane·AcOH stands out as a valuable resource for chemists seeking to innovate in both research and industrial applications.

Synonyms
N-Trityl-1,6-hexanediamine acetate salt
CAS Number
325708-26-7
Purity
≥ 99% (HPLC)
Molecular Formula
C25H30N2·C2H4O2
Molecular Weight
418.6
MDL Number
MFCD01632434
PubChem ID
16210987
Melting Point
120 - 127 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
N-Trityl-1,6-hexanediamine acetate salt
CAS Number
325708-26-7
Purity
≥ 99% (HPLC)
Molecular Formula
C25H30N2·C2H4O2
Molecular Weight
418.6
MDL Number
MFCD01632434
PubChem ID
16210987
Melting Point
120 - 127 °C
Appearance
White powder
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

Trityl-1,6-diaminohexane·AcOH is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in the development of new drugs targeting neurological disorders.
  • Bioconjugation: It is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems and diagnostic tools.
  • Polymer Chemistry: The compound plays a role in creating functionalized polymers, which can be tailored for specific applications in coatings, adhesives, and materials science.
  • Research in Biochemistry: It is valuable in studying protein interactions and enzyme activity, providing insights into biochemical pathways and potential therapeutic targets.
  • Analytical Chemistry: This chemical is utilized in various analytical techniques, including chromatography, to separate and analyze complex mixtures effectively.

Citations