19240
Butyramide
≥98.0% (T)
Synonym(s):
Amide C4
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CH3CH2CH2CONH2
CAS Number:
Molecular Weight:
87.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-776-4
Beilstein/REAXYS Number:
1361528
MDL number:
Product Name
Butyramide, ≥98.0% (T)
InChI 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)
Looking for similar products? Visit Product Comparison Guide
Related Categories
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.
Storage Class
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
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
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
Rajendra Singh et al.
Bioprocess and biosystems engineering, 41(8), 1225-1232 (2018-05-12)
Butyramide is a commodity chemical having wide range of applications from material science to biological sciences including synthesis of therapeutic drugs, hydroxamic acids, and electrorheological fluids. The nitrile hydratase protein of Bacillus sp. APB-6 was explored to develop an efficient
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service