07260
6-Aminohexanoic acid
≥98.5% (NT)
Sinonimo/i:
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
Formula condensata:
H2N(CH2)5CO2H
Numero CAS:
Peso molecolare:
131.17
Beilstein:
906872
Numero CE:
Numero MDL:
Codice UNSPSC:
12352202
ID PubChem:
NACRES:
NA.77
Prodotti consigliati
Livello qualitativo
Saggio
≥98.5% (NT)
Punto di fusione
207-209 °C (dec.) (lit.)
Stringa SMILE
NCCCCCC(O)=O
InChI
1S/C6H13NO2/c7-5-3-1-2-4-6(8)9/h1-5,7H2,(H,8,9)
SLXKOJJOQWFEFD-UHFFFAOYSA-N
Informazioni sul gene
human ... PLAT(5327) , PLG(5340)
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Descrizione generale
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.
Applicazioni
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.
Azioni biochim/fisiol
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.
Altre note
Improves solubilization of membrane proteins in electrophoresis
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
404.6 - 408.2 °F
Punto d’infiammabilità (°C)
207 - 209 °C
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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