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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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
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)
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
Zirconium-mediated conversion of amides to nitriles: a surprising additive effect.
Rebecca T Ruck et al.
Angewandte Chemie (International ed. in English), 43(40), 5375-5377 (2004-10-07)
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