Peptide Synthesis Reagents

T4P, 4-methylpiperidine and trityl chloride support different synthesis tasks: peptide coupling, Fmoc deprotection and protecting-group chemistry. They are not direct substitutes. Select the product against the intended reaction step, substrate, process conditions and required impurity profile.

Compare the Reagents

Synthesis task Product Role Information needed for quotation
Peptide and amide coupling n-Butylphosphonic Anhydride (T4P)
CAS 163755-62-2
Condensation reagent for amide, ester and peptide coupling Required concentration, solvent, specification and quantity
Fmoc deprotection 4-Methylpiperidine
CAS 626-58-4
Base evaluated as an alternative to piperidine for Fmoc deprotection Intended process, target grade, specification and quantity
Protecting-group chemistry Trityl chloride
CAS 76-83-5
Reagent for introducing trityl protecting groups Substrate or functionality, target grade, specification and quantity

Products

n-Butylphosphonic Anhydride (T4P)

CAS 163755-62-2. A condensation reagent for amide, ester and peptide coupling. Available as a 50% solution in ethyl acetate, THF, DCM or diethyl carbonate. For reaction context and work-up considerations, see the T4P coupling application overview.

4-Methylpiperidine

CAS 626-58-4. A saturated nitrogen heterocycle evaluated as a base and as an alternative to piperidine for Fmoc deprotection.

Trityl chloride

CAS 76-83-5. Triphenylmethyl chloride is used to introduce trityl protecting groups in peptide, amino-acid and nucleoside synthesis.

What to Include in an Enquiry

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Product availability, the applicable specification, packaging and batch documentation are confirmed before quotation. Suitability for a particular route should be assessed against the buyer's substrates and process conditions.

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