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217700

Sigma-Aldrich

DL-2-Aminocaprylic acid

99%

Synonym(s):

DL-2-Aminooctanoic acid

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100 MG
$236.00

$236.00

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100 MG
$236.00

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

$236.00

Available to ship onApril 18, 2025Details

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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

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This Item
A0637292915488917
DL-2-Aminocaprylic acid 99%

217700

DL-2-Aminocaprylic acid

DL-2-Aminoadipic acid ≥99%

A0637

DL-2-Aminoadipic acid

2-Pyrrolidone-5-carboxylic acid 99%

292915

2-Pyrrolidone-5-carboxylic acid

DL-Alanine-2,3,3,3-d4 98 atom % D

488917

DL-Alanine-2,3,3,3-d4

assay

99%

assay

≥99%

assay

99%

assay

99% (CP)

mp

260 °C (dec.) (lit.)

mp

196-198 °C (lit.)

mp

183-185 °C (lit.)

mp

289 °C (dec.) (lit.)

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

-

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

-

application(s)

peptide synthesis

application(s)

-

application(s)

peptide synthesis

application(s)

-

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)

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    MKBL8593V
    STBB7662V
    STBB7662
    04409MH
    02528LH

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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
    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)
    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
    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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