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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:
6404-29-1
Molecular Weight:
231.29
Beilstein:
2049561
MDL number:
MFCD00037798
UNSPSC Code:
12352209
PubChem Substance ID:
57647407
NACRES:
NA.22
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Quality Level

100

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.[1][2] Introduction of an aminocaproyl spacer arm in affinity chromatography.[3][4]

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCBT8222
BCBK1304V
1430415V
1430415
1212742

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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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