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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

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About This Item

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

Quality Level

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

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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’.

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Affinity chromatography of carboxypeptidase B.
M Sokolovsky
Methods in enzymology, 34, 411-414 (1974-01-01)
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
J. Frank et al.
Helvetica Chimica Acta, 60, 2550-2550 (1977)
The literature on affinity chromatography.
M Wilchek et al.
Methods in enzymology, 34, 3-10 (1974-01-01)

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