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284637

Sigma-Aldrich

7-Aminoheptanoic acid

98%

Synonym(s):

7-Aminooenanthic acid

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About This Item

Linear Formula:
H2N(CH2)6CO2H
CAS Number:
929-17-9
Molecular Weight:
145.20
Beilstein:
906887
EC Number:
213-197-5
MDL number:
MFCD00008242
UNSPSC Code:
12352106
PubChem Substance ID:
24857170
NACRES:
NA.22

Assay

98%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

mp

192-195 °C (lit.)

application(s)

peptide synthesis

SMILES string

NCCCCCCC(O)=O

InChI

1S/C7H15NO2/c8-6-4-2-1-3-5-7(9)10/h1-6,8H2,(H,9,10)

InChI key

XDOLZJYETYVRKV-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Is there any need for a TAFI(a) inhibitor as thrombolytic drug?
Ellen Vercauteren et al.
Thrombosis research, 130(4), 574-575 (2012-07-31)
V S De Serrano et al.
Biochemistry, 32(14), 3540-3548 (1993-04-13)
The involvement of specific aspartic acid (D) and glutamic acid (E) residues of the recombinant (r) kringle 2 (K2) domain of tissue-type plasminogen activator (tPA) in stabilizing its interaction with omega-amino acid ligands has been assessed by examination of these
Tomoyuki Sasaki et al.
Thrombosis research, 130(4), e222-e228 (2012-07-17)
Thrombin-activatable fibrinolysis inhibitor (TAFI) is a plasma zymogen that is activated by thrombin in plasma. In fibrinolytic processes, carboxy-terminal lysine (Lys) residues in partially degraded fibrin are important sites for plasminogen binding and activation, and an active form of TAFI
V S De Serrano et al.
Biochemistry, 31(47), 11698-11706 (1992-12-01)
The properties of the cationic locus within the recombinant (r) kringle 2 domain (residues 180-261) of tissue-type plasminogen activator ([K2tPA]) that are responsible for stabilization of its interaction with the carboxylate moiety of omega-amino acid ligands have been assessed by
A A Ooka et al.
Biospectroscopy, 5(1), 9-17 (1999-04-29)
Surface enhanced Raman spectroscopy (SERS) was used to characterize a homologous series of alpha,omega-amino acids on colloidal gold and silver. Raman and SER spectra of the alpha,omega-amino acids, NH2(CH2)nCOOH (n = 3-7), are presented and analyzed, revealing the probable conformations
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