Boc-D-Leu-OH
Boc-D-Leu-OH (CAS: 16937-99-8), with the molecular formula C11H21NO4 and a molecular weight of 231.29, is a protected derivative of the non-essential amino acid D-leucine. Its N-terminal tert-butyloxycarbonyl (Boc) group facilitates controlled peptide synthesis by preventing unwanted reactions. This compound is primarily utilised in peptide chemistry and organic synthesis for the construction of specific peptide sequences and complex organic molecules.
- IUPAC
- Boc-D-leucine

Peptide Synthesis
Boc-D-Leu-OH serves as a crucial building block in solid-phase and solution-phase peptide synthesis. The Boc protecting group enables sequential coupling of amino acids, allowing for the controlled assembly of peptide chains for research and development purposes.
Organic Synthesis
This compound finds application in general organic synthesis where a protected form of D-leucine is required. It can be incorporated into more complex molecular architectures, contributing to the development of novel chemical entities.
Chemical Biology Research
Boc-D-Leu-OH is employed in chemical biology to create modified peptides or peptidomimetics. These can be used to probe biological pathways, develop diagnostic tools, or explore structure-activity relationships.
| Molecular weight | 231.29 |
|---|---|
| Empirical formula | C11H21NO4 |
| Assay | ≥98.0% (TLC) |
| 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.
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 Boc-D-Leu-OH used for?
+
Boc-D-Leu-OH is primarily used as a protected building block in peptide synthesis and general organic synthesis, allowing for the controlled introduction of D-leucine into peptide chains or complex organic molecules.
What is the CAS number and formula for Boc-D-Leu-OH?
+
The CAS number for Boc-D-Leu-OH is 16937-99-8, and its empirical formula is C11H21NO4.
What grade and purity does Tech Serve Solutions supply for Boc-D-Leu-OH?
+
Tech Serve Solutions supplies Boc-D-Leu-OH with an assay of ≥98.0% (TLC). This product is not represented as USP, BP, or EP grade.
What are the safety and handling precautions for Boc-D-Leu-OH?
+
When handling Boc-D-Leu-OH, it is essential to wear appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter should be used if airborne exposure is possible. The product has a WGK rating of 3 in Germany, indicating a high hazard to water.
How is Boc-D-Leu-OH packed, shipped, and exported?
+
Boc-D-Leu-OH is carefully packed to ensure product integrity during transit. As a global supplier, Tech Serve Solutions exports chemicals worldwide, adhering to relevant shipping and customs regulations.
How can I request a sample or quote for Boc-D-Leu-OH?
+
To request a sample or a quote for Boc-D-Leu-OH, please contact our sales department through the website or by phone, providing your specific requirements.
▶ 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