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

CAS: 79-10-7 Cat. No.: A397753 Formula: C3H4O2 Molecular Weight: 72.06 Beilstein Registry Number: 635743 EC Number: 201-177-9
AVAILABLE TO ORDER
GRADE & PURITY 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
★
Size
USA
Germany (EU)*
Price
Qty
100g
A397753-100g
9 In stock
7 In stock
$19.90
500g
A397753-500g
In stock ≥10
7 In stock
$54.90
Enter a quantity for the sizes you want to add.
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Why this grade

Anhydrous Grade, ≥99%, stabilized with 200 ppm MEHQ Anhydrous Grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature,Argon charged,Desiccated Ships FedEx DG Service Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 1524 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

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.

Specifications

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
Specifications & Purity
Anhydrous Grade, ≥99%, stabilized with 200 ppm MEHQ
Storage
Protected from light,Room temperature,Argon charged,Desiccated
Shipped In
FedEx DG Service
Grade
Anhydrous Grade
Purity
≥99%
Names and Identifiers
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508811675
Canonical Smiles
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)
Isomeric SMILES
C=CC(=O)O
WGK Germany
1
RTECS
AS4375000
UN Number
2218
Packing Group
II
Molecular Weight
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

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
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
Associated Targets(non-human)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

32 results found

Lot NumberCertificate TypeDateItem
A2615024Certificate of AnalysisOct 09, 2026 A397753
F2609175Certificate of AnalysisJun 23, 2026 A397753
F2609184Certificate of AnalysisJun 23, 2026 A397753
F2609185Certificate of AnalysisJun 22, 2026 A397753
C2605194Certificate of AnalysisMar 16, 2026 A397753
D2518096Certificate of AnalysisJan 21, 2026 A397753
B2604044Certificate of AnalysisJun 10, 2025 A397753
F2524157Certificate of AnalysisJun 10, 2025 A397753
F2524156Certificate of AnalysisJun 10, 2025 A397753
F2524118Certificate of AnalysisJun 10, 2025 A397753
F2524112Certificate of AnalysisJun 10, 2025 A397753
C2513187Certificate of AnalysisMar 20, 2025 A397753
H2309582Certificate of AnalysisJun 11, 2024 A397753
L2411301Certificate of AnalysisApr 02, 2024 A397753
J2429198Certificate of AnalysisApr 02, 2024 A397753
I2411032Certificate of AnalysisApr 02, 2024 A397753
D2411145Certificate of AnalysisApr 02, 2024 A397753
D2411144Certificate of AnalysisApr 02, 2024 A397753
D2411143Certificate of AnalysisApr 02, 2024 A397753
D2411142Certificate of AnalysisApr 02, 2024 A397753
D2411141Certificate of AnalysisApr 02, 2024 A397753
F2419071Certificate of AnalysisJun 14, 2023 A397753
F2314408Certificate of AnalysisJun 14, 2023 A397753
H2309576Certificate of AnalysisJun 14, 2023 A397753
C2310632Certificate of AnalysisMar 17, 2023 A397753
A2212048Certificate of AnalysisOct 21, 2022 A397753
I2212477Certificate of AnalysisSep 01, 2022 A397753
I2212478Certificate of AnalysisSep 01, 2022 A397753
I2212479Certificate of AnalysisSep 01, 2022 A397753
I2212480Certificate of AnalysisSep 01, 2022 A397753
A2417123Certificate of AnalysisSep 01, 2022 A397753
E2227114Certificate of AnalysisJun 01, 2022 A397753
Chemical and Physical Properties
SolubilitySoluble in water, chloroform, ethanol, methanol, and DMF.
SensitivityHygroscopic,Light & Air sensitive.
Refractive Index1.4192-1.4212
Flash Point(°F)119.3 °F - closed cup
Flash Point(°C)48.5 °C - closed cup
Boil Point(°C)139°C
Melt Point(°C)13°C
Molecular Weight72.060 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
Documents & Articles
Innovative Materials for Glass Ionomer Cements (GICs): Dental Applications
Stimulus-responsive materials for intelligent drug delivery systems
RAFT Polymerization
Designing Temperature and pH Sensitive NIPAM Based Polymers
The Guide to Anhydrous Grade for Reagents
Materials Can “Switch”: How Smart Polymers Respond to Temperature, pH, and Light (with Experimental Selection Tips & Product Navigation)
How Organic Acids “Stabilize a System”: Selection Logic via the pH Window, Salt Forms, and Metal-Ion Management (with a navigation guide to Tables A–E)
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
Solution Calculators
Reviews

Customer Reviews

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