Fmoc-D-His(Trt)-OH
Fmoc-D-His(Trt)-OH (CAS: 135610-90-1) is a protected D-histidine derivative used extensively in peptide synthesis. Its chemical formula is C40H33N3O4, with a molecular weight of 619.71 g/mol. The compound features the Fmoc (9-fluorenylmethoxycarbonyl) protecting group on the alpha-amino function and a trityl (Trt) group on the imidazole nitrogen of D-histidine. This combination facilitates controlled peptide chain elongation in solid-phase synthesis and solution-phase methodologies. Available from Tech Serve Solutions.
- IUPAC
- Fmoc-N(im)-trityl-D-histidine
- Synonyms
- Fmoc-D-His(Trt)-OH

Solid-Phase Peptide Synthesis (SPPS)
Fmoc-D-His(Trt)-OH is a key building block in SPPS for incorporating D-histidine residues into peptide sequences. The Fmoc group allows for orthogonal deprotection strategies, while the trityl group offers robust protection for the imidazole side chain during coupling steps.
Chemical Biology Research
This derivative enables the synthesis of complex peptides and peptidomimetics for investigating biological pathways, protein-ligand interactions, and enzyme mechanisms where modified histidine residues are crucial.
Pharmaceutical Intermediate Synthesis
Used in the development of novel therapeutic agents, Fmoc-D-His(Trt)-OH aids in the construction of peptide-based drugs or drug candidates that require specific histidine modifications for efficacy or stability.
Development of Peptide Libraries
Facilitates the creation of diverse peptide libraries for high-throughput screening in drug discovery and proteomics, allowing for the systematic exploration of structure-activity relationships.
| Molecular weight | 619.71 |
|---|---|
| Empirical formula | C40H33N3O4 |
| Assay | 97% (HPLC) |
| Optical activity | [α]22/D -85.0°, c = 1% in chloroform |
| Storage temperature | 2-8°C |
| Melting point | 141-146 °C |
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.
What is Fmoc-D-His(Trt)-OH used for?
+
Fmoc-D-His(Trt)-OH is primarily used as a protected building block in peptide synthesis, particularly for incorporating D-histidine residues into peptide chains using Fmoc chemistry in solid-phase or solution-phase methods.
What are the CAS number and chemical formula for Fmoc-D-His(Trt)-OH?
+
The CAS number is 135610-90-1, and the chemical formula is C40H33N3O4.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Fmoc-D-His(Trt)-OH with a purity of 97% (HPLC). This product is intended for research and chemical synthesis purposes and is not represented as USP, BP, EP, or any other pharmacopoeia grade.
What are the safety and handling considerations for Fmoc-D-His(Trt)-OH?
+
This compound is classified under WGK Germany 3, indicating a high hazard to water. It should be handled with appropriate personal protective equipment in a well-ventilated area, avoiding release into the environment.
How is Fmoc-D-His(Trt)-OH stored and shipped?
+
Fmoc-D-His(Trt)-OH should be stored at 2-8°C. TSS ensures appropriate packaging and adherence to regulations for global export and supply.
How can I request a quote or sample for Fmoc-D-His(Trt)-OH?
+
Please contact our sales team via the website or direct inquiry to request a quote or sample for Fmoc-D-His(Trt)-OH.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis