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217700

Sigma-Aldrich

DL-2-Aminocaprylic acid

99%

Synonym(s):

DL-2-Aminooctanoic acid

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About This Item

Linear Formula:
CH3(CH2)5CH(NH2)CO2H
CAS Number:
644-90-6
Molecular Weight:
159.23
EC Number:
211-424-2
MDL number:
MFCD00008102
UNSPSC Code:
12352106
PubChem Substance ID:
24853027
NACRES:
NA.22

Quality Level

100

assay

99%

form

solid

reaction suitability

reaction type: solution phase peptide synthesis

mp

260 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

CCCCCCC(N)C(O)=O

InChI

1S/C8H17NO2/c1-2-3-4-5-6-7(9)8(10)11/h7H,2-6,9H2,1H3,(H,10,11)

InChI key

AKVBCGQVQXPRLD-UHFFFAOYSA-N

Related Categories

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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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Seon-Hee Kim et al.
PLoS neglected tropical diseases, 6(10), e1868-e1868 (2012-11-15)
Fatty acid (FA) binding proteins (FABPs) of helminths are implicated in acquisition and utilization of host-derived hydrophobic substances, as well as in signaling and cellular interactions. We previously demonstrated that secretory hydrophobic ligand binding proteins (HLBPs) of Taenia solium metacestode
Arik Dahan et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 108, 78-85 (2017-06-20)
The enzyme phospholipase A
Milica Markovic et al.
Pharmaceutics, 11(4) (2019-04-19)
In ulcerative colitis (UC), the inflammation is localized in the colon, and one of the successful strategies for colon-targeting drug delivery is the prodrug approach. In this work, we present a novel phospholipid (PL)-based prodrug approach, as a tool for
Paper chromatography of 56 amino compounds using phenol and butanol-acetic acid as solvents with illustrative chromatograms of normal and abnormal urines.
T E PARRY
Clinica chimica acta; international journal of clinical chemistry, 2(2), 115-125 (1957-04-01)
Sarah A Almahboub et al.
Applied microbiology and biotechnology, 102(2), 789-799 (2017-11-28)
Terminal modification of peptides is frequently used to improve their hydrophobicity. While N-terminal modification with fatty acids (lipidation) has been reported previously, C-terminal lipidation is limited as it requires the use of linkers. Here we report the use of a
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