423548
N-Isopropylmethacrylamide
97%
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About This Item
Linear Formula:
H2C=C(CH3)CONHCH(CH3)2
CAS Number:
Molecular Weight:
127.18
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
237-331-7
MDL number:
InChI key
YQIGLEFUZMIVHU-UHFFFAOYSA-N
InChI
1S/C7H13NO/c1-5(2)7(9)8-6(3)4/h6H,1H2,2-4H3,(H,8,9)
SMILES string
CC(C)NC(=O)C(C)=C
assay
97%
mp
89-91 °C (lit.)
Related Categories
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 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Sonal Deshpande et al.
Soft matter, 14(20), 4169-4177 (2018-04-25)
RNAi is emerging as a promising technology for treatment of various diseases due to its ability to silence specific target genes. To date, a number of nanoparticle based formulations have been reported for the delivery of small interfering RNA (siRNA)
Shalini Saxena et al.
Journal of colloid and interface science, 455, 93-100 (2015-06-10)
We investigate the influence of microgel composition on phase behavior of binary microgel dispersions using poly(N-isopropylacrylamide) microgels cross-linked with 5 mol% and 1 mol% N,N'-methylenebis(acrylamide), or poly(N-isopropylmethacrylamide) microgels cross-linked with 5 mol% N,N'-methylenebis(acrylamide). We then explore the dispersion phase behavior
Loryn E Theune et al.
Materials science & engineering. C, Materials for biological applications, 100, 141-151 (2019-04-06)
Macromolecular bioactives, like proteins and peptides, emerged as highly efficient therapeutics. The main limitation for their clinical application is their instability and potential immunogenicity. Thus, controlled delivery systems able protect the proteins prior release are highly on demand. In the
Timo Brändel et al.
Polymers, 11(8) (2019-08-03)
The present study focuses on the development of multiresponsive core-shell microgels and the manipulation of their swelling properties by copolymerization of different acrylamides-especially N-isopropylacrylamide (NIPAM), N-isopropylmethacrylamide (NIPMAM), and NNPAM-and acrylic acid. We use atomic force microscopy for the dry-state characterization
Adriana M Mihut et al.
Science advances, 3(9), e1700321-e1700321 (2017-09-21)
We have seen a considerable effort in colloid sciences to copy Nature's successful strategies to fabricate complex functional structures through self-assembly. This includes attempts to design colloidal building blocks and their intermolecular interactions, such as creating the colloidal analogs of
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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