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Documentos Principais

07260

Sigma-Aldrich

6-Aminohexanoic acid

≥98.5% (NT)

Sinônimo(s):

6-Aminocaproic acid, 6-ACA, Aca, Acp, Aha, Ahx, acikaprin, afibrin, amicar, ε-Aminocaproic acid, 6-Aminohexanoic acid, EACA

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About This Item

Fórmula linear:
H2N(CH2)5CO2H
Número CAS:
Peso molecular:
131.17
Beilstein:
906872
Número CE:
Número MDL:
Código UNSPSC:
12352202
ID de substância PubChem:
NACRES:
NA.77

Nível de qualidade

Ensaio

≥98.5% (NT)

pf

207-209 °C (dec.) (lit.)

cadeia de caracteres SMILES

NCCCCCC(O)=O

InChI

1S/C6H13NO2/c7-5-3-1-2-4-6(8)9/h1-5,7H2,(H,8,9)

chave InChI

SLXKOJJOQWFEFD-UHFFFAOYSA-N

Informações sobre genes

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Descrição geral

6-Aminohexanoic acid, or 6-aminocaproic acid, acts as an inhibitor of serine proteases. It shares structural similarities with the natural amino acid lysine but lacks an α-amino group.

Aplicação

6-Aminohexanoic acid has been used as a component of the growth medium for tenogenic differentiation of mesenchymal stem cells. It has also been used in the preparation of modified graphene quantum dots.

Ações bioquímicas/fisiológicas

Lysine analog. Promotes rapid dissociation of plasmin, thereby inhibiting the activation of plasminogen and subsequent fibrinolysis.
Lysine analog. Promotes rapid dissociation of plasmin, thereby inhibiting the activation of plasminogen and subsequent fibrinolysis. Reported to inhibit plasminogen binding to activated platelets. An early report indicated that it inhibits the activation of the first component of the complement system. Binds and inactivates Carboxypeptidase B.

Outras notas

Improves solubilization of membrane proteins in electrophoresis

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

404.6 - 408.2 °F

Ponto de fulgor (°C)

207 - 209 °C

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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