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01697

Supelco

Acrylamide solution

40% in H2O, for molecular biology

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About This Item

Fórmula linear:
CH2=CHCONH2
Número CAS:
79-06-1
Peso molecular:
71.08
Beilstein:
6185892
Número MDL:
MFCD00008032
Código UNSPSC:
12352111
eCl@ss:
39031205
ID de substância PubChem:
329747347
NACRES:
ND.02

grau

for molecular biology

Nível de qualidade

100

forma

liquid

concentração

40% in H2O

técnica(s)

electrophoresis: suitable

Impurezas

DNases, none detected
 RNases, none detected
 phosphatases, none detected
 proteases, none detected

traços de ânion

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤50 mg/kg

traços de cátion

Ca: ≤5 mg/kg
Cd: ≤1 mg/kg
Co: ≤1 mg/kg
Cr: ≤1 mg/kg
Cu: ≤1 mg/kg
Fe: ≤1 mg/kg
K: ≤10 mg/kg
Mg: ≤5 mg/kg
Mn: ≤1 mg/kg
Na: ≤50 mg/kg
Ni: ≤1 mg/kg
Pb: ≤1 mg/kg
Zn: ≤1 mg/kg

adequação

in accordance for electrophoresis test

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

NC(=O)C=C

InChI

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

chave InChI

HRPVXLWXLXDGHG-UHFFFAOYSA-N

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Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Peripheral nervous system

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
BCCC3516
BCBV0798
BCBN3237V
BCBH4170V
BCBD7503V

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Acrilamida certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

08267

Acrilamida

N,N′-Methylenebisacrylamide for electrophoresis, special grade for molecular biology

Sigma-Aldrich

1.01546

N,N′-Methylenebisacrylamide

N,N′-Methylenebisacrylamide powder, for molecular biology, suitable for electrophoresis, ≥99.5%

Sigma-Aldrich

M7279

N,N′-Methylenebisacrylamide

Acrilamida analytical standard

Supelco

23701

Acrilamida

Acrilamida purum, ≥98.0% (GC)

Sigma-Aldrich

01700

Acrilamida

Acrylamide/Bis-acrylamide for molecular biology, BioReagent, 19:1 (ratio)

Sigma-Aldrich

A2917

Acrylamide/Bis-acrylamide

Jonas S Laursen et al.
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
Arianna Rath et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(39), 15668-15673 (2013-09-11)
SDS/PAGE is universally used in biochemistry, cell biology, and immunology to resolve minute protein amounts readily from tissue and cell extracts. Although molecular weights of water-soluble proteins are reliably determined from their SDS/PAGE mobility, most helical membrane proteins, which comprise
Janneke G F Hogervorst et al.
Critical reviews in toxicology, 40(6), 485-512 (2010-02-23)
Since 2002, it is known that the probable human carcinogen acrylamide is present in commonly consumed carbohydrate-rich foods, such as French fries and potato chips. In this review, the authors discuss the body of evidence on acrylamide carcinogenicity from both
Janneke G F Hogervorst et al.
Carcinogenesis, 35(5), 1032-1038 (2014-01-09)
Acrylamide, a probable human carcinogen, is present in heat-treated carbohydrate-rich foods. Epidemiological studies have not shown a clear association between acrylamide intake and colorectal cancer (CRC) risk. This may be due to the molecular heterogeneity in colorectal tumors, which was
Chun-Hua Lu et al.
Nano letters, 13(3), 1298-1302 (2013-02-21)
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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HPLC Analysis of Acrylamide and Acrylic Acid on Discovery® HS F5

HPLC Analysis of Acrylamide and Acrylic Acid on Discovery® HS F5

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