Hydroxypropyl methacrylate (HPMA) - ≥97%, stabilized with s0.02% 4-methoxyphenol , CAS No.27813-02-1

CAS: 27813-02-1 Cat. No.: H109880 Peso molecular: 144.17 Beilstein Registry Number: 1752228 Número EC: 248-666-3
Disponible para pedir
GRADE & PURITY ≥97% stabilized with s0.02% 4-methoxyphenol
Synonyms
2-Hydroxypropylmethacrylate | 2-hydroxypropyl 2-methylprop-2-enoate
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25ml
H109880-25ml
9

11,90US$

13,90US$
Guardar 2,00 US$ (14.39%)
100ml
H109880-100ml
10
15,90US$
250ml
H109880-250ml
4
23,90US$
500ml
H109880-500ml
3
41,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥97%, stabilized with s0.02% 4-methoxyphenol for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

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 53 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
2-Hydroxypropylmethacrylate | 2-hydroxypropyl 2-methylprop-2-enoate
Especificaciones y pureza
≥97%, stabilized with s0.02% 4-methoxyphenol
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥97%
Nombres e identificadores
Pubchem Sid504752458
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504752458
Sonrisas canónicasCC(COC(=O)C(=C)C)O
IUPAC Name2-hydroxypropyl 2-methylprop-2-enoate
InChIKeyVHSHLMUCYSAUQU-UHFFFAOYSA-N
INCHI1S/C7H12O3/c1-5(2)7(9)10-4-6(3)8/h6,8H,1,4H2,2-3H3
Isómeros SMILES CC(COC(=O)C(=C)C)O
WGK Alemania 1
RTECS UD3442500
Peso molecular 144.17
Beilstein 1752228
Reaxy-Rn 1752228
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1752228&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
ClaseCarboxylic acids and derivatives
SubclassCarboxylic acid derivatives
Intermediate Tree Nodes Carboxylic acid esters - Alpha,beta-unsaturated carboxylic esters
Direct ParentEnoate esters
Alternative Parents Secondary alcohols  Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Enoate ester - Secondary alcohol - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as enoate esters. These are an alpha,beta-unsaturated carboxylic ester of general formula R1C(R2)=C(R3)C(=O)OR4 (R4= organyl compound) in which the ester C=O function is conjugated to a C=C double bond at the alpha,beta position.
External Descriptors enoate ester
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

47 results found

Lot NumberCertificate TypeFechaArticulo
H2407697Certificate of AnalysisMay 19, 2026 H109880
L2519016Certificate of AnalysisJun 16, 2025 H109880
G2504238Certificate of AnalysisJun 16, 2025 H109880
G2504236Certificate of AnalysisJun 16, 2025 H109880
G2504235Certificate of AnalysisJun 16, 2025 H109880
G2504215Certificate of AnalysisJun 16, 2025 H109880
G2504173Certificate of AnalysisJun 16, 2025 H109880
G2504172Certificate of AnalysisJun 16, 2025 H109880
E2620190Certificate of AnalysisJun 16, 2025 H109880
E2607021Certificate of AnalysisJun 16, 2025 H109880
G2322742Certificate of AnalysisApr 18, 2025 H109880
D2510301Certificate of AnalysisMar 28, 2025 H109880
D2510302Certificate of AnalysisMar 28, 2025 H109880
D2510300Certificate of AnalysisMar 28, 2025 H109880
D2510299Certificate of AnalysisMar 28, 2025 H109880
D2308666Certificate of AnalysisJan 07, 2025 H109880
D2308667Certificate of AnalysisJan 07, 2025 H109880
D2308675Certificate of AnalysisJan 07, 2025 H109880
D2308690Certificate of AnalysisJan 07, 2025 H109880
D2308681Certificate of AnalysisJan 07, 2025 H109880
D2308679Certificate of AnalysisJan 07, 2025 H109880
H2422086Certificate of AnalysisJul 26, 2024 H109880
H2422063Certificate of AnalysisJul 26, 2024 H109880
H2422062Certificate of AnalysisJul 26, 2024 H109880
D2423443Certificate of AnalysisMar 15, 2024 H109880
D2423442Certificate of AnalysisMar 15, 2024 H109880
D2423440Certificate of AnalysisMar 15, 2024 H109880
D2423441Certificate of AnalysisMar 15, 2024 H109880
G2412132Certificate of AnalysisMar 15, 2024 H109880
D2423439Certificate of AnalysisMar 15, 2024 H109880
D2423446Certificate of AnalysisMar 15, 2024 H109880
D2423447Certificate of AnalysisMar 15, 2024 H109880
G2521055Certificate of AnalysisMar 15, 2024 H109880
D2423445Certificate of AnalysisMar 15, 2024 H109880
G2521085Certificate of AnalysisMar 15, 2024 H109880
G2322748Certificate of AnalysisJun 29, 2023 H109880
G2322739Certificate of AnalysisJun 29, 2023 H109880
G2107174Certificate of AnalysisApr 12, 2023 H109880
D2308664Certificate of AnalysisMar 28, 2023 H109880
D2308669Certificate of AnalysisMar 28, 2023 H109880
D2308692Certificate of AnalysisMar 28, 2023 H109880
C2310610Certificate of AnalysisMar 17, 2023 H109880
B2102033Certificate of AnalysisDec 12, 2022 H109880
H1822037Certificate of AnalysisMay 10, 2022 H109880
C2031032Certificate of AnalysisJan 18, 2022 H109880
I2221011Certificate of AnalysisApr 09, 2021 H109880
B2328232Certificate of AnalysisApr 09, 2021 H109880

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Propiedades químicas y físicas
SensibilidadLight sensitive
Índice de refracción1.447
Punto de inflamación (°F)203 °F
Punto de inflamación (°C)95 °C
Punto de ebullición (°C)57°C
Peso molecular144.170 g/mol
XLogP31.000
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass144.079 Da
Monoisotopic Mass144.079 Da
Topological Polar Surface Area46.500 Ų
Heavy Atom Count10
Formal Charge0
Complexity140.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Structural and Performance Design of Acrylic Resins for Coatings: Monomer Composition, Key Parameters, and Film Formation/Curing Mechanisms
Guide to Selecting Polyurethane Coating Systems: Application Analysis for Wood, Flooring, Plastics, Automotive, and Industrial Protection
How Do Isocyanates and Polyols Affect the Performance of Polyurethane Coating Films: Structure, Raw Material Selection, and Performance Design Essentials
When Should You Choose Silicone Resin? Selection Comparison with Epoxy, Acrylic, Polyurethane, Fluororesin, and Other Coating Resins
Polyurethane Coating Resins: Not a Single Resin, but a Designable High-Performance System
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
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
Citations of This Product
Referencias
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5. Tianwei Zhang, Shanjun Gao, Jianying Yu, Yanheng He, Xiaobing Han, Ronghua Zhuang.  (2023)  Preparation and performance of self-healing SBS modified bitumen based on dynamic disulfide bonds.  CONSTRUCTION AND BUILDING MATERIALS,      [PMID:] [10.1016/j.conbuildmat.2023.132394]
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