Boc-Homoser-OH
Boc-L-homoserine (CAS: 41088-86-2), with the molecular formula C9H17NO5 and a molecular weight of 219.23 g/mol, is a protected amino acid derivative. It serves as a valuable building block in organic synthesis and peptide chemistry. Its primary applications lie in research and development, particularly for the synthesis of modified peptides and complex organic molecules.
- IUPAC
- Boc-L-homoserine
- Synonyms
- Boc-L-homoserine

Peptide Synthesis
Boc-L-homoserine is employed as a protected amino acid in solid-phase and solution-phase peptide synthesis. It allows for controlled incorporation into peptide chains, enabling the creation of novel peptide analogues.
Organic Synthesis Intermediate
This compound acts as a versatile intermediate in the synthesis of various organic molecules. Its functional groups can be further modified for the construction of complex structures in medicinal chemistry and materials science.
Biochemical Research
Used in biochemical studies and as a reagent for investigating protein structure and function. It is a useful tool for researchers exploring amino acid modifications and their biological implications.
| Molecular weight | 219.23 |
|---|---|
| Empirical formula | C9H17NO5 |
| Storage temperature | −20°C |
| 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-L-homoserine used for?
+
Boc-L-homoserine (CAS: 41088-86-2) is primarily used as a protected amino acid building block in peptide synthesis and as an intermediate in organic synthesis for research and development purposes.
What is the CAS number and formula for Boc-L-homoserine?
+
The CAS number for Boc-L-homoserine is 41088-86-2, and its molecular formula is C9H17NO5.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Boc-L-homoserine primarily for research and development purposes. The specific grade and purity are not indicated as USP, BP, or EP. Customers should refer to the Certificate of Analysis for detailed specifications.
What are the safety and handling precautions for Boc-L-homoserine?
+
Handling Boc-L-homoserine requires appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter is recommended. The substance is classified with a WGK Germany rating of 3, indicating a high hazard to water.
How is Boc-L-homoserine packed, shipped, and exported?
+
Boc-L-homoserine is typically stored at -20°C. Tech Serve Solutions adheres to strict protocols for packing, shipping, and exporting fine chemicals globally, ensuring product integrity and regulatory compliance.
How can I request a sample or quote for Boc-L-homoserine?
+
To request a sample or a quote for Boc-L-homoserine, please contact the Tech Serve Solutions sales team through our website or by phone, providing the product name and CAS number (41088-86-2).
▶ Related products
![(±)-(E)-4-Ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide (C8H13N3O4) — chemical structure, CAS 138472-01-2; Biochemicals & Reagents, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F138472-01-2.png&w=3840&q=75)
(±)-(E)-4-Ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide
C8H13N3O4
Biochemicals & Reagents![(±)-(E)-4-Ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1-yl-nicotinamide (C14H18N4O4) — chemical structure, CAS 162626-99-5; Biochemicals & Reagents, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F162626-99-5.png&w=3840&q=75)
(±)-(E)-4-Ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1-yl-nicotinamide
C14H18N4O4
Biochemicals & Reagents
(±)-2,5-Dimethoxy-4-bromoamphetamine hydrobromide
Biochemicals & Reagents

(±)-2-(p-Methoxyphenoxy)propionic acid
C10H12O4
Biochemicals & Reagents
(±)-2-Amino-6,7-dihydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide
C10H13NO2·HBr
Biochemicals & Reagents
(±)-2-Hydroxydecanoic acid
C10H20O3
Biochemicals & Reagents
(±)-3-Hydroxydecanoic acid
C10H20O3
Biochemicals & Reagents
(±)-3-Hydroxyoctanoic acid
C8H16O3
Biochemicals & Reagents▶ 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