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Merck
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Documentos

01-1300

Sigma-Aldrich

Acrilamida

≥98.0%

Sinónimos:

2-Propenamida, Amida del ácido acrílico

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About This Item

Fórmula lineal:
CH2=CHCONH2
Número de CAS:
79-06-1
Peso molecular:
71.08
Beilstein/REAXYS Number:
605349
MDL number:
MFCD00008032
UNSPSC Code:
41105305
PubChem Substance ID:
329747217

vapor density

2.45 (vs air)

vapor pressure

0.03 mmHg ( 40 °C)

assay

≥98.0%

form

solid

availability

available only in Japan

bp

125 °C/25 mmHg (lit.)

mp

82-86 °C (lit.)

SMILES string

NC(=O)C=C

InChI

1S/C3H5NO/c1-2-3(4)5/h2H,1H2,(H2,4,5)

InChI key

HRPVXLWXLXDGHG-UHFFFAOYSA-N

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Suitability

for electrophoresis

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Carc. 1B - Eye Irrit. 2 - Muta. 1B - Repr. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 1 Oral

target_organs

Peripheral nervous system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

280.4 °F

flash_point_c

138 °C

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Acrylamide (AA) is known as a neurotoxin in humans and it is classified as a probable human carcinogen by the International Agency of Research on Cancer. AA is produced as by-product of the Maillard reaction in starchy foods processed at
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Proceedings of the National Academy of Sciences of the United States of America, 110(39), 15668-15673 (2013-09-11)
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Copolymer chains consisting of acrylamide units and guanine (G)-containing oligonucleotide-tethered acrylamide units undergo, in the presence of K(+) ions, cross-linking by G-quadruplexes to yield a hydrogel. The hydrogel is dissociated upon addition of 18-crown-6 ether that traps the K(+) ions.
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Journal of the American Chemical Society, 135(7), 2835-2844 (2013-01-25)
Non-natural peptide analogs have significant potential for the development of new materials and pharmacologically active ligands. One such architecture, the β-peptoids (N-alkyl-β-alanines), has found use in a variety of biologically active compounds but has been sparsely studied with respect to
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