293393
Hexanoamide
98%
Synonym(s):
Caproamide
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About This Item
Linear Formula:
CH3(CH2)4CONH2
CAS Number:
Molecular Weight:
115.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
211-024-8
MDL number:
Assay:
98%
InChI key
ALBYIUDWACNRRB-UHFFFAOYSA-N
InChI
1S/C6H13NO/c1-2-3-4-5-6(7)8/h2-5H2,1H3,(H2,7,8)
SMILES string
CCCCCC(N)=O
assay
98%
mp
100-102 °C (lit.)
functional group
amide
General description
Hexanoamide is the most rapidly hydrolysed substrate for amidase from Aspergillus nidulans. Zirconium mediated conversion of hexanoamide to hexanenitrile has been reported.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
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)
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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
Daniel O Reddy et al.
Bulletin of environmental contamination and toxicology, 104(2), 253-258 (2020-01-04)
Polycyclic aromatic hydrocarbons (PAHs) and naphthenic acids (NAs) are toxic contaminants of environmental concern found in process water and mature fine tailings, or tailings, from the oil sands industry. BioTiger™, a patented microbial consortium of twelve natural environmental isolates, was
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