Acrylic acid - Anhydrous Grade, ≥99%, stabilized with 200 ppm MEHQ , CAS No.79-10-7

CAS: 79-10-7 Cat. No.: A397753 Formule: C3H4O2 Poids moléculaire: 72.06 Beilstein Registry Number: 635743 Numéro CE: 201-177-9
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Anhydrous Grade ? Anhydrous grade — water removed and packaged dry for moisture-sensitive chemistry. Use in reactions where even trace water would interfere or quench. ≥99% stabilized with 200 ppm MEHQ
Synonyms
Glacial acrylic acid | XPA | 2-Propenoic acid | ACRYLIC ACID [IARC] | RCRA waste number U008 | Carbopol 934 (TN) | Carbopol 940 (TN) | EINECS 201-177-9 | Jurimer AC 10P | Versicol E 7 | Viscon 103 | ACRYLIC ACID (IARC) | Aron A 10H | Acroleic acid | Arald
Storage
Protected from light,Room temperature,Argon charged,Desiccated
Shipped In
FedEx DG Service
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Taille
Allemagne (EU)
USA*
Prix
Qté
100g
A397753-100g
7 En stock
9 En stock
17,27€
500g
A397753-500g
7 En stock
En stock ≥10
47,64€
Enter a quantity for the sizes you want to add.
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Pourquoi cette qualité

Anhydrous Grade, ≥99%, stabilized with 200 ppm MEHQ Anhydrous Grade pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Protected from light,Room temperature,Argon charged,Desiccated Expédition FedEx DG Service. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 1545 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Acrylic acid is an unsaturated carboxylic acid that is commonly used as a versatile building block in the chemical industry because of its reactive double bond between the carbon and oxygen atoms. It is used to prepare various acrylic acid-based polymers, which are used for various applications such as adhesives, paints & coatings, medical devices, organic semiconductors,thin-film transistors, hydrogels and lithium-ion batteries. Additionally, acrylic acid also serves as one of the polyelectrolytes in the self-assembled polymeric film used for hydrogen generation.
Application
Acrylic acid can be primarily used as a monomer to produce various acrylic polymers, including polyacrylic acid, polymethyl methacrylate (PMMA), acrylonitrile butadiene styrene (ABS), and many others. These polymers exhibit a wide range of properties, such as transparency, scratch-resistant, flexibility, and resistance to water and chemicals, which make them valuable materials in various applications. Acrylic acid is also used as a key component in the synthesis of superabsorbent polymers(SAPs). These polymers possess a unique ability to quickly absorb and retain large quantities of water. Due to their excellent properties, SAPs have been widely used in many fields, such as drug-delivery systems, chemical industry, and personal care, etc.
Acrylic acid can also be used as:
A key component in the preparation of copolymer binder, which helps to optimize the performance of lithium-ion batteries.
A surface modifier for the carbon nanotubes with poly(acrylic acid) in order to improve adhesion and dispersion of the nanotubes in the oxide semiconductor matrix for thin-film transistor applications.
A reactive monomer for the surface modification of polydimethylsiloxane (PDMS)through a simultaneous polymerization process with ethylene glycol dimethacrylate. Modified PDMS potentially applied in new applications fields such as microfluidics or biomedical devices.
A precursor for the synthesis of cashew gum/acrylic acid nanoparticles via the copolymerization process. The use of acrylic acid in the synthesis is to introduce hydrophilic functional groups into the cashew gum backbone, thereby improving its solubility in water and increasing its compatibility with other hydrophilic materials.
AAc is used in preparing monodispersed poly (N-isopropylacryamide) (PNIPAM)/AAc microgels.[8] AAc has been plasma-deposited on surfaces for cell culture applications.Surface modification of poly(ethylene terephthalate) (PET) films via UV-induced graft copolymerization with AAc has been reported.AAc is used primarily as an intermediate in the production of acrylates.

Spécifications

Synonymes
Glacial acrylic acid | XPA | 2-Propenoic acid | ACRYLIC ACID [IARC] | RCRA waste number U008 | Carbopol 934 (TN) | Carbopol 940 (TN) | EINECS 201-177-9 | Jurimer AC 10P | Versicol E 7 | Viscon 103 | ACRYLIC ACID (IARC) | Aron A 10H | Acroleic acid | Arald
Spécifications et pureté
Anhydrous Grade, ≥99%, stabilized with 200 ppm MEHQ
Conditions de stockage de stockage
Protected from light,Room temperature,Argon charged,Desiccated
Expédié en
FedEx DG Service
Grade
Anhydrous Grade
Pureté
≥99%
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508811675
Sourires canoniques
C=CC(=O)O
IUPAC Name
prop-2-enoic acid
InChIKey
NIXOWILDQLNWCW-UHFFFAOYSA-N
INCHI
1S/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5)
Isomères SMILES
C=CC(=O)O
WGK Allemagne
1
RTECS
AS4375000
Numéro ONU
2218
Groupe d'emballage
II
Poids moléculaire
72.06
Beilstein
635743
Reaxy-Rn
635743
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635743&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassAcrylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentAcrylic acids
Alternative Parents Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Acrylic acid - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as acrylic acids. These are organic compounds containing acrylic acid CH2=CHCO2H.
External Descriptors Unsaturated fatty acids
Structure 3D
Modèle de structure chimique interactif





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CHAT Tchem Choline acetylase (63 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
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LMNA Tbio Prelamin-A/C (36751 Activities)
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Cibles associées (non humaines)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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32 results found

Lot NumberCertificate TypeDateArticle
A2615024A2615024Certificate of AnalysisOct 09, 2026 A397753
F2609175F2609175Certificate of AnalysisJun 23, 2026 A397753
F2609184F2609184Certificate of AnalysisJun 23, 2026 A397753
F2609185F2609185Certificate of AnalysisJun 22, 2026 A397753
C2605194C2605194Certificate of AnalysisMar 16, 2026 A397753
D2518096D2518096Certificate of AnalysisJan 21, 2026 A397753
B2604044B2604044Certificate of AnalysisJun 10, 2025 A397753
F2524157F2524157Certificate of AnalysisJun 10, 2025 A397753
F2524156F2524156Certificate of AnalysisJun 10, 2025 A397753
F2524118F2524118Certificate of AnalysisJun 10, 2025 A397753
F2524112F2524112Certificate of AnalysisJun 10, 2025 A397753
C2513187C2513187Certificate of AnalysisMar 20, 2025 A397753
H2309582H2309582Certificate of AnalysisJun 11, 2024 A397753
L2411301L2411301Certificate of AnalysisApr 02, 2024 A397753
J2429198J2429198Certificate of AnalysisApr 02, 2024 A397753
I2411032I2411032Certificate of AnalysisApr 02, 2024 A397753
D2411145D2411145Certificate of AnalysisApr 02, 2024 A397753
D2411144D2411144Certificate of AnalysisApr 02, 2024 A397753
D2411143D2411143Certificate of AnalysisApr 02, 2024 A397753
D2411142D2411142Certificate of AnalysisApr 02, 2024 A397753
D2411141D2411141Certificate of AnalysisApr 02, 2024 A397753
F2419071F2419071Certificate of AnalysisJun 14, 2023 A397753
F2314408F2314408Certificate of AnalysisJun 14, 2023 A397753
H2309576H2309576Certificate of AnalysisJun 14, 2023 A397753
C2310632C2310632Certificate of AnalysisMar 17, 2023 A397753
A2212048A2212048Certificate of AnalysisOct 21, 2022 A397753
I2212477I2212477Certificate of AnalysisSep 01, 2022 A397753
I2212478I2212478Certificate of AnalysisSep 01, 2022 A397753
I2212479I2212479Certificate of AnalysisSep 01, 2022 A397753
I2212480I2212480Certificate of AnalysisSep 01, 2022 A397753
A2417123A2417123Certificate of AnalysisSep 01, 2022 A397753
E2227114E2227114Certificate of AnalysisJun 01, 2022 A397753
Propriétés chimiques et physiques
SolubilitéSoluble in water, chloroform, ethanol, methanol, and DMF.
SensibilitéHygroscopic,Light & Air sensitive.
Indice de réfraction1.4192-1.4212
Point d'éclair (°F)119.3 °F - closed cup
Point d'éclair (°C)48.5 °C - closed cup
Point d'ébullition (°C)139°C
Point de fusion (°C)13°C
Poids moléculaire72.060 g/mol
XLogP30.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass72.0211 Da
Monoisotopic Mass72.0211 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count5
Formal Charge0
Complexity55.900
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQ et articles
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Application and Selection Guide for Alkyd Resin Coatings: Advantages, Limitations, Formulation Control, and Modification Directions
Structural and Performance Design of Acrylic Resins for Coatings: Monomer Composition, Key Parameters, and Film Formation/Curing Mechanisms
When Should You Choose Silicone Resin? Selection Comparison with Epoxy, Acrylic, Polyurethane, Fluororesin, and Other Coating Resins
Vinyl Acetate-Acrylic Emulsion (Vinyl Acrylic Emulsion): A Cost-Performance Balance Solution for Architectural Coatings
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VC/VAc Resins and Their Modification: An Analysis of VC/VAc Vinyl Resins for Coatings and Inks
How to Select Vinyl-Related Resins: Building Formulation Judgment Based on Substrate, Performance Targets, and Failure Risks
Waterborne Resin Technology Explained: Waterborne Forms, Performance Balance, and a Technology Map
Guide to Common Waterborne Resin Types and Application-Based Selection: How to Choose Acrylics, PUD, Waterborne Epoxy, Waterborne Alkyd, VAE, and Related Chemicals
From Water to Film: Film-Formation Mechanisms and Performance Development of Waterborne Emulsions and Dispersions
Diagnosis of Coating Performance Issues and Selection of Resin Modification Routes
Structural Design Logic of Common Resin Modification Technologies: Molecular Chain Structure, Functional Groups, Phase Structure, Crosslinked Networks, and Hybrid/Functional Design
Resin Polarity in Coating Formulations: From Molecular Structure to Dissolution, Compatibility, Interfacial Interactions, and Formulation Design
From Structure to Rheology: How Carbomer Forms Gel Structures and Enables Thickening, Suspension, and Auxiliary Emulsion Stabilization
Structure–Performance Relationship of Polyquaterniums in Hair and Personal Care Formulations: Smoothing Conditioning, Antistatic Performance, Film Formation, and Deposition Behavior
Key Variable in the Long-Term Stability of Waterborne Pigment Concentrates: How Dispersant Molecular Weight Distribution (MWD) Affects Pigment Dispersion, Surface Adsorption-Layer Formation, and Storage Stability
Citations of This Product
Calculateurs de solution
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