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Merck
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Documentos Principais

A7824

Sigma-Aldrich

6-Aminocaproic acid

BioUltra, ≥99%

Sinônimo(s):

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

fonte biológica

synthetic (organic)

grau

biotech. grade

linha de produto

BioUltra

Ensaio

≥99%

Formulário

powder

técnica(s)

cell culture | mammalian: suitable

Impurezas

≤0.005% Phosphorus (P)
≤0.1% Insoluble matter

resíduo de ignição

≤0.1%

pf

207-209 °C (dec.) (lit.)

solubilidade

H2O: 0.5 M, clear, colorless

traços de ânion

chloride (Cl-): ≤0.05%
sulfate (SO42-): ≤0.05%

traços de cátion

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%

temperatura de armazenamento

room temp

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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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.

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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