Skip to Content
Merck
All Photos(1)

Documents

15395

Sigma-Aldrich

Boc-6-Ahx-OH

≥99.0% (T)

Synonym(s):

6-(Boc-amino)caproic acid, 6-(Boc-amino)hexanoic acid, Boc-6-aminohexanoic acid

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CH3)3CO2CNH(CH2)5CO2H
CAS Number:
6404-29-1
Molecular Weight:
231.29
Beilstein:
2049561
MDL number:
MFCD00037798
UNSPSC Code:
12352209
PubChem Substance ID:
57647407
NACRES:
NA.22

Assay

≥99.0% (T)

form

solid

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

35-40 °C

application(s)

peptide synthesis

storage temp.

2-8°C

SMILES string

CC(C)(C)OC(=O)NCCCCCC(O)=O

InChI

1S/C11H21NO4/c1-11(2,3)16-10(15)12-8-6-4-5-7-9(13)14/h4-8H2,1-3H3,(H,12,15)(H,13,14)

InChI key

RUFDYIJGNPVTAY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Other Notes

Protected derivative to introduce the ε-aminocaproyl moiety in various compounds. Introduction of an aminocaproyl spacer arm in affinity chromatography.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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 J Schroit et al.
Biochemistry, 22(15), 3617-3623 (1983-07-19)
An efficient method for the synthesis and purification of a variety of iodinated phospholipid analogues is described. 1-Acyl-2-[[[3-(3-[125I]iodo-4-hydroxyphenyl)- propionyl]amino]caproyl]phosphatidylcholine (125I-PC) was prepared by alkylation of 1-acyl-2-(aminocaproyl)phosphatidylcholine with monoiodinated Bolton-Hunter reagent. 125I-Labeled phosphatidic acid, phosphatidylethanolamine, and phosphatidylserine were produced from 125I-PC
The literature on affinity chromatography.
M Wilchek et al.
Methods in enzymology, 34, 3-10 (1974-01-01)
J. Frank et al.
Helvetica Chimica Acta, 60, 2550-2550 (1977)
Affinity chromatography of carboxypeptidase B.
M Sokolovsky
Methods in enzymology, 34, 411-414 (1974-01-01)

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