4-Fmoc-1-piperazineacetic acid hydrate

CAS 180576-05-0C21H22N2O4 · xH2OChemical Synthesis

Tech Serve Solutions offers 4-Fmoc-1-piperazineacetic acid hydrate (CAS: 180576-05-0, C21H22N2O4 · xH2O). This compound has a molecular weight of 366.41 g/mol (anhydrous basis). Primarily utilised in chemical synthesis and peptide chemistry, it serves as a valuable building block. Its structure makes it suitable for modifications in drug discovery and the development of unnatural amino acid derivatives. Available from TSS with an assay of ≥97.0%.

IUPAC: 4-Fmoc-piperazin-1-ylacetic acid
Synonyms: 4-Fmoc-piperazin-1-ylacetic acid

Email us

4-Fmoc-1-piperazineacetic acid hydrate (C21H22N2O4 · xH2O) — chemical structure, CAS 180576-05-0; Chemistry, fine chemical supplied by Tech Serve Solutions

Chemical BiologyChemical SynthesisOthersPeptide Chemistry

01 /Applications

Peptide Synthesis

This compound is employed as a protected amino acid derivative in solid-phase peptide synthesis (SPPS) and solution-phase methods. It allows for the controlled incorporation of modified piperazine moieties into peptide sequences.

Chemical Synthesis

Its reactive functional groups make it a versatile intermediate for constructing more complex organic molecules. It can be used in the development of novel chemical entities for research purposes.

Drug Discovery

As a building block in medicinal chemistry, it aids in the synthesis of potential therapeutic agents. The piperazine core is a common feature in many pharmacologically active compounds.

Unnatural Amino Acid Derivatives

It serves as a precursor for creating non-proteinogenic amino acids, expanding the scope of peptide and protein research and engineering.

02 /Properties

Molecular weight	366.41 (anhydrous basis)
Empirical formula	C21H22N2O4 · xH2O
Assay	≥97.0%
Storage temperature	2-8°C

03 /Safety & handling

Protective equipment	Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Water hazard class (WGK, DE)	3

Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.

04 /Identifiers & registry

CAS number

180576-05-0

MDL number

MFCD00674524

05 /Quality & supply

Documentation

Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.

Supply & logistics

Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.

06 /Frequently asked questions

What is 4-Fmoc-1-piperazineacetic acid hydrate used for?

This compound is primarily used in chemical synthesis, peptide chemistry, drug discovery, and as a building block for unnatural amino acid derivatives. It is a protected amino acid derivative suitable for peptide synthesis.

What is the CAS number and formula for 4-Fmoc-1-piperazineacetic acid hydrate?

The CAS number is 180576-05-0, and the empirical formula is C21H22N2O4 · xH2O.

What grade and purity does Tech Serve Solutions supply?

Tech Serve Solutions supplies 4-Fmoc-1-piperazineacetic acid hydrate with an assay of ≥97.0%. This product is intended for research and chemical synthesis purposes and is not represented as USP, BP, EP, or pharmacopoeia grade.

How should 4-Fmoc-1-piperazineacetic acid hydrate be handled?

Handle with appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter is recommended. The compound is classified under WGK-Germany 3, indicating a high hazard to water.

How is 4-Fmoc-1-piperazineacetic acid hydrate shipped?

This product is typically stored at 2-8°C and is carefully packed and exported by Tech Serve Solutions, adhering to all necessary regulations for chemical transport.

How can I request a quote or sample?

To request a quote or sample of 4-Fmoc-1-piperazineacetic acid hydrate, please contact the Tech Serve Solutions sales team via our website or direct inquiry.