08267
Acrylamide
certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Synonyme(s) :
2-Propenamide, Acrylic acid amide
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About This Item
Formule linéaire :
CH2=CHCONH2
Numéro CAS:
Poids moléculaire :
71.08
Numéro Beilstein :
605349
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24
Produits recommandés
Qualité
certified reference material
TraceCERT®
Niveau de qualité
Densité de vapeur
2.45 (vs air)
Pression de vapeur
0.03 mmHg ( 40 °C)
Fabricant/nom de marque
Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Technique(s)
HPLC: suitable
gas chromatography (GC): suitable
Point d'ébullition
125 °C/25 mmHg (lit.)
Pf
82-86 °C (lit.)
Application(s)
cleaning products
cosmetics
environmental
food and beverages
personal care
Format
neat
Chaîne SMILES
NC(=O)C=C
InChI
1S/C3H5NO/c1-2-3(4)5/h2H,1H2,(H2,4,5)
Clé InChI
HRPVXLWXLXDGHG-UHFFFAOYSA-N
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Description générale
This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here
Application
- Advanced Synthesis Techniques: Acrylamide is utilized in the synthesis of acyl cyclopentaquinolinones, showcasing its versatility in heterocyclic scaffold construction and acyl group introduction, proving essential for organic synthesis in pharmaceutical research (Xue et al., 2024).
- Material Development for Energy Sectors: Acrylamide-based polymers are applied in developing temperature-sensitive materials for oil and gas drilling, highlighting its importance in creating responsive materials for challenging environments (Yang et al., 2024).
- Innovations in Polymer Science: The use of acrylamide in the numerical simulation of polyacrylamide hydrogel via thermally initiated frontal polymerization provides insights into the controlled synthesis of hydrogels, useful in biomedical applications (Yi et al., 2024).
- Health Impact Studies: Research includes acrylamide in studies examining the inhibition of harmful Maillard reaction products by polyphenols, relevant for understanding chronic diseases linked to dietary acrylamide (Ye et al., 2024).
Conditionnement
Bottomless glass bottle. Contents are inside inserted fused cone.
Produits recommandés
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Informations légales
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
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
Organes cibles
Peripheral nervous system
Code de la classe de stockage
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
280.4 °F - closed cup
Point d'éclair (°C)
138 °C - closed cup
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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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