293393
Hexanoamide
98%
Synonym(s):
Caproamide
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About This Item
Linear Formula:
CH3(CH2)4CONH2
CAS Number:
Molecular Weight:
115.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
98%
mp
100-102 °C (lit.)
functional group
amide
SMILES string
CCCCCC(N)=O
InChI
1S/C6H13NO/c1-2-3-4-5-6(7)8/h2-5H2,1H3,(H2,7,8)
InChI key
ALBYIUDWACNRRB-UHFFFAOYSA-N
General description
Hexanoamide is the most rapidly hydrolysed substrate for amidase from Aspergillus nidulans. Zirconium mediated conversion of hexanoamide to hexanenitrile has been reported.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Jianfei Zheng et al.
Bioconjugate chemistry, 19(6), 1227-1234 (2008-05-30)
Molecular conjugates of hormone receptor-ligands with molecular probes or functional domains are finding diverse applications in chemical biology. Whereas many examples of hormone conjugates that target steroid hormone receptors have been reported, practical ligand conjugates that target the nuclear thyroid
Alexandra Thomas et al.
Cancers, 12(8) (2020-08-23)
Pancreatic cancer remains a recalcitrant neoplasm associated with chemoresistance and high fatality. Because it is frequently resistant to apoptosis, exploiting autophagic cell death could offer a new treatment approach. We repurpose echinomycin, an antibiotic encapsulated within a syndecan-1 actively targeted
Aliphatic and enantioselective amidases: from hydrolysis to acyl transfer activity.
D Fournand et al.
Journal of applied microbiology, 91(3), 381-393 (2001-09-15)
Jyoti Choithani et al.
Analytical biochemistry, 357(2), 240-248 (2006-08-26)
Synthesis of a new heterobifunctional reagent, N-(3-triethoxysilylpropyl)-6-(N-maleimido)-hexanamide (TPMH), for the preparation of oligonucleotide microarrays is described. Its triethoxysilyl function is specific toward virgin glass surface and maleimide function undergoes conjugate addition to 3'- or 5'-thiol-modified oligonucleotides. The construction of microarrays
R W Fleischman et al.
Journal of environmental pathology and toxicology, 3(5-6), 149-170 (1980-06-01)
As a part of the National Cancer Institute's effort to screen environmental and occupational chemicals for chronic toxicity and carcinogenicity, the amides acetamide, hexanamide, adipamide, urea, and p-tolylurea were fed to male and female C57B1/6 mice and Fischer 344 rats
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