Accéder au contenu
Merck
Toutes les photos(5)

Documents

A2504

Sigma-Aldrich

6-Aminocaproic acid

≥99% (titration), powder

Synonyme(s) :

ε-Aminocaproic acid, 6-Aminohexanoic acid, EACA

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(5)

About This Item

Formule linéaire :
H2N(CH2)5CO2H
Numéro CAS:
60-32-2
Poids moléculaire :
131.17
Numéro Beilstein :
906872
Numéro CE :
200-469-3
Numéro MDL:
MFCD00008238
Code UNSPSC :
12352202
ID de substance PubChem :
24890662
Nomenclature NACRES :
NA.77

Source biologique

synthetic

Pureté

≥99% (titration)

Forme

powder

Technique(s)

cell culture | mammalian: suitable

Couleur

white

Pf

207-209 °C (dec.) (lit.)

Solubilité

H2O: 50 mg/mL

Chaîne SMILES 

NCCCCCC(O)=O

InChI

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

Clé InChI

SLXKOJJOQWFEFD-UHFFFAOYSA-N

Informations sur le gène

human ... PLAT(5327) , PLG(5340)
rat ... Ppm1a(24666)

Vous recherchez des produits similaires ? Visite Guide de comparaison des produits

Catégories apparentées

Application

EACA is directly soluble in water at 25 mg/ml. As an inhibitor of plasmin it is has been utilized in the clotting buffer for fibrinogen assays. This buffer is 10 mM potassium and sodium phosphate, pH 6.4, with 0.20 g CaCl2, 5 g 6-Aminohexanoic acid, 1 g sodium azide, and 9 g NaCl in 1 liter. The buffer is stable indefinitely at room temperature.

Actions biochimiques/physiologiques

EACA is reported to inhibit chymotrypsin, Factor VIIa, lysine carbo­xy­peptidase, plasmin, and plasminogen activator.
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.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

404.6 - 408.2 °F

Point d'éclair (°C)

207 - 209 °C

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Les clients ont également consulté

Slide 1 of 4

1 of 4

Benzamidine hydrochloride hydrate ≥99%

Sigma-Aldrich

B6506

Benzamidine hydrochloride hydrate

8-Aminooctanoic acid 99%

Sigma-Aldrich

855294

8-Aminooctanoic acid

7-Aminoheptanoic acid 98%

Sigma-Aldrich

284637

7-Aminoheptanoic acid

Benzamidine ≥95.0%

Sigma-Aldrich

12072

Benzamidine

Kazuki Yamamoto et al.
Lab on a chip, 21(10), 1897-1907 (2021-05-20)
Engineered three-dimensional models of neuromuscular tissues are promising for use in mimicking their disorder states in vitro. Although several models have been developed, it is still challenging to mimic the physically separated structures of motor neurons (MNs) and skeletal muscle
Moamen Bydoun et al.
Molecular oncology, 12(11), 1895-1916 (2018-07-17)
Pancreatic cancer is arguably the deadliest cancer type. The efficacy of current therapies is often hindered by the inability to predict patient outcome. As such, the development of tools for early detection and risk prediction is key for improving outcome
Brian Hutton et al.
BMJ (Clinical research ed.), 345, e5798-e5798 (2012-09-13)
To estimate the relative risks of death, myocardial infarction, stroke, and renal failure or dysfunction between antifibrinolytics and no treatment following the suspension of aprotinin from the market in 2008 for safety reasons and its recent reintroduction in Europe and
Lajos Gera et al.
Peptides, 34(2), 433-446 (2012-02-22)
Peptide agonists and antagonists of both bradykinin (BK) B(1) and B(2) receptors (B(1)R, B(2)R) are known to tolerate to a certain level N-terminal sequence extensions. Using this strategy, we produced and characterized the full set of fluorescent ligands by extending
Ai Kia Yip et al.
Biophysical journal, 104(1), 19-29 (2013-01-22)
Cells sense the rigidity of their substrate; however, little is known about the physical variables that determine their response to this rigidity. Here, we report traction stress measurements carried out using fibroblasts on polyacrylamide gels with Young's moduli ranging from
Afficher tous les articles scientifiques apparentés

Articles

Chymotrypsin

Analytical Enzyme Chymotrypsin: Chymotrypsin is produced in the acinar cells of the pancreas as the inactive precursor, chymotrypsinogen.

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique