217700
DL-2-Aminocaprylic acid
99%
Sinônimo(s):
DL-2-Aminooctanoic acid
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About This Item
Fórmula linear:
CH3(CH2)5CH(NH2)CO2H
Número CAS:
Peso molecular:
159.23
Número CE:
Número MDL:
Código UNSPSC:
12352106
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
99%
Formulário
solid
adequação da reação
reaction type: solution phase peptide synthesis
pf
260 °C (dec.) (lit.)
aplicação(ões)
peptide synthesis
cadeia de caracteres SMILES
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)
chave InChI
AKVBCGQVQXPRLD-UHFFFAOYSA-N
Categorias relacionadas
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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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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