Skip to Content
Merck
CN
All Photos(3)

Documents

Safety Information

B4645

Sigma-Aldrich

Boc-Homoser-OH

>99%

Sign Into View Organizational & Contract Pricing

Synonym(s):
Boc-L-homoserine
Empirical Formula (Hill Notation):
C9H17NO5
CAS Number:
Molecular Weight:
219.23
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26

Assay

>99%

form

powder

color

white

application(s)

peptide synthesis

storage temp.

−20°C

SMILES string

CC(C)(C)OC(=O)NC(CCO)C(O)=O

InChI

1S/C9H17NO5/c1-9(2,3)15-8(14)10-6(4-5-11)7(12)13/h6,11H,4-5H2,1-3H3,(H,10,14)(H,12,13)

InChI key

PZEMWPDUXBZKJN-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Biochem/physiol Actions

Boc-L-homoserine is N-terminal protected α amino acid used in organic synthesis of compounds such as the functionalizable methionine surrogate azidohomoalanine.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

A James Link et al.
Nature protocols, 2(8), 1884-1887 (2007-08-19)
This protocol describes a synthetic route to the non-canonical amino acid azidohomoalanine (AHA) using protected homoserine as a starting material. An alternative route to AHA is presented in a companion paper. This synthesis can be completed in 5 days.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service