All Photos(1)

194301

Sigma-Aldrich

6-Acetamidohexanoic acid

99%

Linear Formula:
CH3CONH(CH2)5CO2H
CAS Number:
Molecular Weight:
173.21
EC Number:
MDL number:
PubChem Substance ID:

assay

99%

mp

102-104 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC(=O)NCCCCCC(O)=O

InChI

1S/C8H15NO3/c1-7(10)9-6-4-2-3-5-8(11)12/h2-6H2,1H3,(H,9,10)(H,11,12)

InChI key

WDSCBUNMANHPFH-UHFFFAOYSA-N

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Certificate of Origin

Allergic contact dermatitis to acexamic acid.
Ana Margarida Soares Reis et al.
Contact dermatitis, 58(4), 241-242 (2008-03-21)
A García-Plaza et al.
Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva, 88(11), 757-762 (1996-11-01)
A multicentric double-blind trial comparing 600 mg/d of Zinc Acexamate (ACZ) and 40 mg/d of Famotidine (FMT) in the short term treatment of acute duodenal ulcer included 199 patients, diagnosed by endoscopy. One-hundred and five patients received ACZ and 94
C Navarro et al.
Prostaglandins, leukotrienes, and essential fatty acids, 50(6), 305-310 (1994-06-01)
Gastrotoxic activities of different non-steroidal anti-inflammatory drugs (NSAIDs) (diclofenac, indomethacin, ketoprofen, naproxen and piroxicam) administered per os were compared with their ability to inhibit gastric prostaglandin E2 (PGE2) synthesis in the rat. In a parallel study, effects of pretreatment with
Seth Chitayat et al.
Biochemistry, 46(7), 1732-1742 (2007-02-01)
The plasma lipoprotein lipoprotein(a) [Lp(a)] comprises a low-density lipoprotein (LDL)-like particle covalently attached to the glycoprotein apolipoprotein(a) [apo(a)]. Apo(a) consists of multiple tandem repeating kringle modules, similar to plasminogen kringle IV (designated KIV1-KIV10), followed by modules homologous to the kringle
H Y Li et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 30(1), 17-20 (1995-01-01)
Zinc acexamate (ZAC) is a new antiulcer drug. This paper reports the pharmacokinetics of ZAC in rats after single oral administration. The concentrations in biological samples were detected by spectrophotometry. This study shows that the concentration-time curve of ZAC in

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