19240
Butyramide
≥98.0% (T)
Sinónimos:
Amide C4
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Fórmula lineal:
CH3CH2CH2CONH2
Número CAS:
Peso molecular:
87.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-776-4
Beilstein/REAXYS Number:
1361528
MDL number:
Assay:
≥98.0% (T)
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Permítanos ayudarleInChI key
DNSISZSEWVHGLH-UHFFFAOYSA-N
InChI
1S/C4H9NO/c1-2-3-4(5)6/h2-3H2,1H3,(H2,5,6)
SMILES string
CCCC(N)=O
assay
≥98.0% (T)
mp
114-116 °C
solubility
alcohol: soluble(lit.), diethyl ether: slightly soluble(lit.), water: soluble(lit.)
functional group
amide
Quality Level
Gene Information
rat ... Ggt1(116568)
Categorías relacionadas
Application
Butyramide was used in the synthesis of hydroxamic acids, electrorheological fluids and β-amodoorganotin compounds. It was used as substrate of (+)-γ-lactamase to develop a microreactor to study enzyme stability, activity, kinetics and substrate specificity.
Clase de almacenamiento
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Jiahua Jiang et al.
PloS one, 7(3), e34283-e34283 (2012-04-06)
We have recently synthesized novel N-alkylated amino acid-derived hydroxamate, 2-[Benzyl-(2-nitro-benzenesulfonyl)-amino]-N-hydroxy-3-methyl-N-propyl-butyramide (NAHA). Here, we evaluate the anticancer activity of NAHA against highly invasive human breast cancer cells MDA-MB-231 in vitro and in vivo. Cell growth was evaluated by MTT and soft
L J Hellebrekers et al.
Laboratory animals, 24(3), 200-204 (1990-07-01)
A number of experiments was carried out to determine the sequence of events leading to death following administration of the euthanizing agent T61. Simultaneous recordings of the EMG, EEG, ECG and end-tidal CO2 (dogs only) were obtained in acutely instrumented
Jiang Hong et al.
Biophysical journal, 109(1), 144-153 (2015-07-15)
Biopolymer homeostasis underlies the health of organisms, and protective osmolytes have emerged as one strategy used by Nature to preserve biopolymer homeostasis. However, a great deal remains unknown about the mechanism of action of osmolytes. Trehalose, as a prominent example
Maja D Vitorović-Todorović et al.
Bioorganic & medicinal chemistry, 18(3), 1181-1193 (2010-01-12)
Synthesis and anticholinesterase activity of 4-aryl-4-oxo-N-phenyl-2-aminylbutyramides, novel class of reversible, moderately potent cholinesterase inhibitors, are reported. Simple substituent variation on aroyl moiety changes anti-AChE activity for two orders of magnitude; also substitution and type of hetero(ali)cycle in position 2 of
B P O'Hara et al.
Protein engineering, 13(2), 129-132 (2000-03-10)
The AmiC protein in Pseudomonas aeruginosa is the negative regulator and ligand receptor for an amide-inducible aliphatic amidase operon. In the wild-type PAC1 strain, amidase expression is induced by acetamide or lactamide, but not by butyramide. A mutant strain of
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