A7824

6-Aminocaproic acid

≥99%, BioUltra

• Synonym(s): ε-Aminocaproic acid, 6-Aminohexanoic acid, EACA
• Linear Formula: H₂N(CH₂)₅CO₂H
• CAS Number: 60-32-2
• Molecular Weight: 131.17
• Beilstein: 906872
• EC Number: 200-469-3
• MDL number: MFCD00008238
• UNSPSC Code: 12352202
• PubChem Substance ID: 24278238
• NACRES: NA.77

Properties

• biological source: synthetic (organic)
• product line: BioUltra
• Assay: ≥99%
• form: powder
• technique(s): cell culture | mammalian: suitable
• impurities: ≤0.005% Phosphorus (P); ≤0.1% Insoluble matter
• ign. residue: ≤0.1%
• mp: 207-209 °C (dec.) (lit.)
• solubility: H₂O: 0.5 M, clear, colorless
• anion traces: chloride (Cl^-): ≤0.05%; sulfate (SO₄^2-): ≤0.05%
• cation traces: Al: ≤0.0005%; Ca: ≤0.005%; Cu: ≤0.0005%; Fe: ≤0.0005%; K: ≤0.005%; Mg: ≤0.001%; NH₄⁺: ≤0.05%; Na: ≤0.02%; Pb: ≤0.001%; Zn: ≤0.0005%
• storage temp.: room temp
• SMILES string: NCCCCCC(O)=O
• InChI: 1S/C6H13NO2/c7-5-3-1-2-4-6(8)9/h1-5,7H2,(H,8,9)
• InChI key: SLXKOJJOQWFEFD-UHFFFAOYSA-N
• Gene Information: human ... PLAT(5327) , PLG(5340) ; rat ... Ppm1a(24666)

Description

Biochem/physiol Actions

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.

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 2
• Flash Point(F): 404.6 - 408.2 °F
• Flash Point(C): 207 - 209 °C
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves