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Merck

217700

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
NACRES:
NA.22
PubChem Substance ID:
24853027
UNSPSC Code:
12352106
EC Number:
211-424-2
MDL number:
MFCD00008102

Key Documents

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Product Name

DL-2-Aminocaprylic acid, 99%

InChI key

AKVBCGQVQXPRLD-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCCCC(N)C(O)=O

assay

99%

form

solid

reaction suitability

reaction type: solution phase peptide synthesis

mp

260 °C (dec.) (lit.)

application(s)

peptide synthesis

Quality Level

100

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1 of 4

This Item
A0637292915488917
DL-2-Aminocaprylic acid 99%

Sigma-Aldrich

217700

DL-2-Aminocaprylic acid

DL-2-Aminoadipic acid ≥99%

Sigma-Aldrich

A0637

DL-2-Aminoadipic acid

2-Pyrrolidone-5-carboxylic acid 99%

Sigma-Aldrich

292915

2-Pyrrolidone-5-carboxylic acid

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

Sigma-Aldrich

488917

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

form

solid

form

powder

form

-

form

solid

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX7362
MKBL8593V
STBB7662V
STBB7662
04409MH

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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)
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
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
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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