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About This Item
Empirical Formula (Hill Notation):
C7H13NO
CAS Number:
Molecular Weight:
127.18
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
MDL number:
InChI
1S/C7H13NO/c1-4-7(9)8(5-2)6-3/h4H,1,5-6H2,2-3H3
SMILES string
CCN(CC)C(=O)C=C
InChI key
OVHHHVAVHBHXAK-UHFFFAOYSA-N
assay
99%
form
liquid
contains
<200 ppm MEHQ as inhibitor
refractive index
n20/D 1.468
density
0.924 at 25 °C
storage temp.
2-8°C
Quality Level
Related Categories
Application
Acrylamide monomer used to make polymers for drug delivery; thermal responsive polymers; and solutions with specifically tuned LCSTs.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
192.0 °F
flash_point_c
88.89 °C
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Nuran Işıklan et al.
Carbohydrate polymers, 218, 112-125 (2019-06-22)
Pectin based micro/nanocarriers display promising properties for biomedical applications. In this study, thermo/pH-responsive chitosan coated pectin-graft-poly(N,N-diethyl acrylamide) (Pec-g-PDEAAm/CS) microcarriers containing 5-Fluorouracil (5-FU) as a model drug were developed. The structure, thermal stability and surface morphology of 5-FU-loaded microcarriers were investigated
Seog-Jin Jeon et al.
Soft matter, 16(3), 688-694 (2019-12-10)
Trilayer polymer films consisting of a thermoresponsive hydrogel, poly(diethyl acrylamide) (PDEAM), sandwiched by rigid layers of a glassy polymer, poly(para-methylstyrene) (PpMS), patterned into parallel striped features are prepared and used to drive temperature-responsive reversible anisotropic expansion. Significant swelling occurs along
Huynh Nguyen Anh Tuan et al.
Polymers, 12(5) (2020-05-21)
A series of semi-interpenetrating polymer network (semi-IPN) hydrogels based on N,N'-diethylacrylamide (DEA) and itaconamic acid (IAM) were synthesized by changing the molar ratio of linear copolymer P(DEA-co-IAM) and DEA monomer. Linear copolymer P(DEA-co-IAM) was introduced into a solution of DEA
Z Ding et al.
Nature, 411(6833), 59-62 (2001-05-03)
Many medical and biotechnological processes rely on controlling and manipulating the molecular-recognition capabilities of proteins. This can be achieved using small molecules capable of competing for protein binding or by changing environmental parameters that affect protein structure and hence binding.
Xiaoyu Zhuang et al.
Journal of the American Society for Mass Spectrometry, 28(2), 341-346 (2016-11-11)
We investigate the influence of three volatile alkylammonium acetate buffers on binding affinities for protein-ligand interactions determined by native electrospray ionization-mass spectrometry (ESI-MS). Four different types of proteins were chosen for this study. A charge-reduction effect was observed for all
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