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07260

Sigma-Aldrich

6-Aminohexanoic acid

≥98.5% (NT)

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Synonym(s):
6-Aminocaproic acid, ε-Aminocaproic acid, 6-Aminohexanoic acid, EACA
Linear Formula:
H2N(CH2)5CO2H
CAS Number:
Molecular Weight:
131.17
Beilstein/REAXYS Number:
906872
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.77

Quality Level

assay

≥98.5% (NT)

mp

207-209 °C (dec.) (lit.)

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

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1 of 4

This Item
A25048.001451021000
6-Aminohexanoic acid ≥98.5% (NT)

07260

6-Aminohexanoic acid

6-Aminocaproic acid ≥99% (titration), powder

A2504

6-Aminocaproic acid

6-Aminohexanoic acid for synthesis

8.00145

6-Aminohexanoic acid

Aminocaproic acid United States Pharmacopeia (USP) Reference Standard

1021000

Aminocaproic acid

mp

207-209 °C (dec.) (lit.)

mp

207-209 °C (dec.) (lit.)

mp

205 °C

mp

207-209 °C (dec.) (lit.)

Quality Level

200

Quality Level

-

Quality Level

200

Quality Level

-

Gene Information

human ... PLAT(5327), PLG(5340)

Gene Information

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

Gene Information

-

Gene Information

human ... PLAT(5327), PLG(5340)

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.

Other Notes

Improves solubilization of membrane proteins in electrophoresis

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

404.6 - 408.2 °F

flash_point_c

207 - 209 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves


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