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

CAS: 79-10-7 Cat. No.: A397753 Fórmula: C3H4O2 Peso molecular: 72.06 Beilstein Registry Number: 635743 Número CE: 201-177-9
Disponível para encomenda
GRAU & PUREZA 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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Tamanho
USA
Alemanha (EU)*
Preço
Qtd
100g
A397753-100g
9 Em stock
7 Em stock
19,90US$
500g
A397753-500g
Em stock ≥10
7 Em stock
54,90US$
Enter a quantity for the sizes you want to add.
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Por que este grau

Anhydrous Grade, ≥99%, stabilized with 200 ppm MEHQ Anhydrous Grade para fluxos de trabalho cromatográficos e analíticos sensíveis que exigem interferência mínima da linha de base.

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Armazenamento e envio

Protected from light,Room temperature,Argon charged,Desiccated Envio FedEx DG Service. Consulte o COA específico do lote para obter as especificações exatas.

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Documentos de qualidade

SDS, COA, ficha técnica e folha de especificações disponíveis para download. COA específico do lote acessível por meio de pesquisa por número de lote.

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Comprovação documental

Citado em 1545 publicações revisadas por pares nas áreas de cromatografia, síntese orgânica e reações de acoplamento cruzado.

Visão geral

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.

Especificações

Sinónimos
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
Especificações e pureza
Anhydrous Grade, ≥99%, stabilized with 200 ppm MEHQ
Condições de armazenamento de armazenamento
Protected from light,Room temperature,Argon charged,Desiccated
Enviado em
FedEx DG Service
Grau
Anhydrous Grade
Pureza
≥99%
Nomes e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508811675
Sorrisos canónicos
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)
SMILES isoméricas
C=CC(=O)O
WGK Alemanha
1
RTECS
AS4375000
Número UN
2218
Grupo de embalagem
II
Peso molecular
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=

Documentação

📋 Ficha de dados de segurança (FDS)

Documento abrangente sobre perigos, manuseamento, armazenamento e conformidade regulamentar.

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✅ Certificado de análise (COA)

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📊 Ficha técnica

Resumo de referência rápida das especificações e aplicações do produto.

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🔬 Folha de especificações

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Dados avançados

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
DescriçãoThis 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
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
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)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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32 results found

Lot NumberCertificate TypeDataItem
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
Propriedades químicas e físicas
SolubilidadeSoluble in water, chloroform, ethanol, methanol, and DMF.
SensibilidadeHygroscopic,Light & Air sensitive.
Índice de refração1.4192-1.4212
Ponto de inflamação (°F)119.3 °F - closed cup
Ponto de inflamação (°C)48.5 °C - closed cup
Ponto de ebulição (°C)139°C
Ponto de fusão (°C)13°C
Peso molecular72.060 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
FAQs e artigos
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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
Vinyl Ester Resin Systems: Structural Features, Curing Mechanism, and Key Application Considerations
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
Calculadoras de soluções
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