07260
6-Aminohexanoic acid
≥98.5% (NT)
Sinónimos:
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 lineal:
H2N(CH2)5CO2H
Número de CAS:
Peso molecular:
131.17
Beilstein:
906872
Número CE:
Número MDL:
Código UNSPSC:
12352202
ID de la sustancia en PubChem:
NACRES:
NA.77
Productos recomendados
Nivel de calidad
Ensayo
≥98.5% (NT)
mp
207-209 °C (dec.) (lit.)
cadena SMILES
NCCCCCC(O)=O
InChI
1S/C6H13NO2/c7-5-3-1-2-4-6(8)9/h1-5,7H2,(H,8,9)
Clave InChI
SLXKOJJOQWFEFD-UHFFFAOYSA-N
Información sobre el gen
human ... PLAT(5327) , PLG(5340)
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Descripción general
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.
Aplicación
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.
Acciones bioquímicas o 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.
Otras notas
Improves solubilization of membrane proteins in electrophoresis
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 2
Punto de inflamabilidad (°F)
404.6 - 408.2 °F
Punto de inflamabilidad (°C)
207 - 209 °C
Equipo de protección personal
dust mask type N95 (US), Eyeshields, Gloves
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