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2-HYDROXY-PROPYL METHACRYLATE (2-HPMA)

2-Hydroxy-Propyl Methacrylate (2-HPMA) is also used as a co-monomer in styrene based unsaturated polyesters, PMMA based acrylic resins and vinyl ester formulations in anchor bolts and chemical fixings.
2-Hydroxy-Propyl Methacrylate (2-HPMA) may also be used in the production of emulsion polymers in combination with other commodity methacrylates and acrylates, notably for textile coatings and textile sizes.

CAS Number: 27813-02-1 (commonly used)
Alternative CAS Number: 923-26-2
EC Number (EINECS): 248-666-3
Molecular Formula: C₇H₁₂O₃
Molecular Weight: 144.17 g/mol

SYNONYMS:
2-Hydroxypropyl Methacrylate, 2-HPMA, HPMA, Methacrylic Acid 2-Hydroxypropyl Ester, β-Hydroxypropyl Methacrylate, 2-Hydroxypropyl 2-Methylacrylate, 2-Hydroxypropyl 2-Methyl-2-Propenoate, Propylene Glycol Monomethacrylate, 2-Propenoic Acid 2-Methyl-2-Hydroxypropyl Ester, 1,2-Propanediol Methacrylate, Hydroxypropyl Methacrylate, Photomer® 2317,2-Hydroxypropyl methacrylate,923-26-2,Acryester HP,beta-Hydroxypropyl methacrylate,2-Hydroxypropyl 2-methyl-2-propenoate,2-Propenoic acid, 2-methyl-, 2-hydroxypropyl ester,METHACRYLIC ACID, 2-HYDROXYPROPYL ESTER,2-HPMA,V9B8S034AW,CHEBI:53440,BLEMMER P,RefChem:87608,GlyTouCan:G03618RH,G03618RH,213-090-3,2-Hydroxypropylmethacrylate,2-hydroxypropyl 2-methylprop-2-enoate,2-Hydroxypropyl 2-methylacrylate,DTXSID1029629,methacrylic acid 2-hydroxypropyl ester,.beta.-hydroxypropyl methacrylate,DSSTox_CID_5934,EINECS 213-090-3,BRN 1752228,UNII-V9B8S034AW,2HPMA,Epitope ID:131322,DSSTox_RID_77971,DSSTox_RID_78619,DSSTox_GSID_25934,DSSTox_GSID_27936,SCHEMBL19017,SCHEMBL166150,SCHEMBL198125,DTXCID805934,2-hydroxy-n-propyl methacrylate,2-hydroxy-3-propyl methacrylate,CHEMBL1873783,SCHEMBL27697323,SCHEMBL28747006,1,2-Propanediol, 1-methacrylate,2-Hydroxypropyl 2-methylacrylate #,Tox21_200694,Tox21_201232,Tox21_202531,2-Hydroxypropyl methacrylate (HPMA),MFCD00004536,AKOS015899917,CS-W011008,NCGC00090806-01,NCGC00090806-02,NCGC00090806-03,NCGC00258248-01,NCGC00258784-01,NCGC00260080-01,AS-59279,CAS-923-26-2,CAS-25703-79-1,CAS-27813-02-1,M0512,NS00014926,Hydroxypropyl methacrylate, mixture of isomers,D93082,2-Propenoic acid,2-methyl-,2-hydroxypropyl ester,Q27124054, HYDROXYPROPYL METHACRYLATE,METHACRYLIC ACID 2-HYDROXYPROPYL ESTER,methacrylic acid, monoester with propane-1,2-diol,2HPMA,L-61040,rocryl410,Photomer 2317,2-Hydroxypropyl meth,CHLUMICRYL HPMA Monomer,Hydroxy propyl ethacrylate,2-Propenoic acid,2-methyl-,monoester with 1,2-propanediol,Methacrylic acid,monoester with 1,2-propanediol,Methacrylic acid,ester with 1,2-propanediol,1,2-Propanediol,monomethacrylate,Hydroxypropyl methacrylate,Rocryl 410,Propylene glycol monomethacrylate,HPMA 98,Bisomer HPMA,HPMA 97,1,2-Propylene glycol methacrylate,Propylene glycol methacrylate,Visiomer HPMA 98,Visiomer MPMA 98,99609-88-8,122413-04-1,124742-02-5,138258-23-8,27072-46-4,30348-68-6,32073-20-4,50851-93-9,50975-16-1,51424-40-9,51480-40-1,63625-57-0,191411-56-0,204013-27-4,Meracryl HPMA, bisomer HPMA, beta-hydroxypropyl methacrylate, Acryester HP, 2hydroxypropyl 2-methacrylate,poly(2-hydroxypropylmethacrylate),2-hydroxypropyl 2-methyl-2-propenoate,2-Propenoicacid,2-methyl-,monoesterwith1,2-propanediol,METHACRYLIC ACID 2-HYDROXYPROPYL ESTER,METHACRYLIC ACID HYDROXYPROPYL ESTER,HYDROXYPROPYL METHACRYLATE,methacrylic acid, monoester with propane-1,2-diol,HYDROXYPROPYL METHACRYLATE, MIXTURE OF I SOMERS, STAB.,HYDROXYPROPYL METHACRYLATE, 97%, MIXTURE OF ISOMERS,METHACRYLIC ACID HYDROXYPROPYL ESTER (MIXTURE OF 2-HYDROXY-N-PROPYL AND 2-HYDROXY-1-METHYLETHYL METHACRYLATE)(STABILIZED WITH MEHQ) 95+%,2-hydroxypropyl 2-methyl-2-propenoate,2-hydroxypropyl 2-methylacrylate,3-hydroxypropyl 2-methylprop-2-enoate,2-hydroxypropyl methacrylate,2-hydroxypropylmethacrylate,methacrylic acid 2-hydroxypropyl ester,methacrylic acid hydroxypropyl ester,methacrylic acid monoester with 1,2-propane diol,methacrylic acid, 2-hydroxypropyl ester,methacrylic acid, monoester with propane-1,2-diol,2-methyl-2-propenoic acid 2-hydroxypropyl ester,1,2-propanediol, monomethacrylate (8CI),2-propenoic acid, 2-methyl-, 2-hydroxypropyl ester,2-propenoic acid, 2-methyl-, monoester with 1,2-propanediol

2-Hydroxy-Propyl Methacrylate (2-HPMA) is a clear, colourless liquid with a characteristic odour.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is an ester of methacrylic acid.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is relatively non-volatile, non-toxic and non-yellowing.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is a clear, colorless liquid with a pungent, sweet odor.
2-Hydroxy-Propyl Methacrylate (2-HPMA) contains low levels of a polymerization inhibitor along with small amounts of methacrylic acid, and propylene oxide.

2-Hydroxy-Propyl Methacrylate (2-HPMA) copolymerizes readily with a wide variety of monomers, and the added hydroxyl groups improve adhesion to surfaces, incorporate cross-linking sites, and impart corrosion, fogging, and abrasion resistance, as well as contribute to low odour, colour, and volatility.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is a white liquid with a light unpleasant odor.
2-Hydroxy-Propyl Methacrylate (2-HPMA) may float or sink in water.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is an ester of Methacrylic acid and is used as a raw material component in the synthesis of polymers.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is a functional hydrophobic hydroxy monomer consisting of a methacrylate group with a characteristic high reactivity and a cyclic hydrophobic group.
2-Hydroxy-Propyl Methacrylate (2-HPMA) forms a homopolymer and copolymer.

Copolymers of 2-Hydroxy-Propyl Methacrylate (2-HPMA) can be prepared with (meth)acrylic acid and its salts, amides, and esters, as well as with (meth)acrylates, acrylonitrile, maleic acid esters, vinyl acetate, vinyl chloride, vinylidene chloride, styrene, butadiene, and other monomers.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a clear, colorless liquid with a pungent, sweet odor.

2-Hydroxy-Propyl Methacrylate (2-HPMA) contains low levels of a polymerization inhibitor along with small amounts of methacrylic acid, and propylene oxide.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used in the manufacture of acrylic polymers for adhesives, inks, and coatings for automotive, appliance and metal applications.

The added hydroxyl groups improve adhesion to surfaces, incorporate cross-link sites, and impart corrosion, fogging, and abrasion resistance.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a clear colorless liquid
Uses of 2-Hydroxy-Propyl Methacrylate (2-HPMA): Monomer for acrylic resins, nonwoven fabric binders, detergent lubricating-oil additives.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is an enoate ester that is the 1-methacryloyl derivative of propane-1,2-diol.
2-Hydroxy-Propyl Methacrylate (2-HPMA) has a role as a polymerisation monomer.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is functionally related to a propane-1,2-diol and a methacrylic acid.

2-Hydroxy-Propyl Methacrylate (2-HPMA), which easily enters into the reaction of accession with a wide range of organic and inorganic substances, is used to synthesize organic low molecular weight substances.
2-Hydroxy-Propyl Methacrylate (2-HPMA), also known as 2-HPMA, is a monofunctional methacrylic monomer commonly used in the formulation of dental composites and sealants.

2-Hydroxy-Propyl Methacrylate (2-HPMA) possesses reactive hydroxyl groups that enable cross-linking and improved mechanical properties, making it a valuable component in dental materials.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a clear, colorless, low-volatility monomer used primarily to produce acrylic polymers, coatings, adhesives, and UV-curable inks.

Known for improving adhesion, flexibility, and chemical/weather resistance, 2-Hydroxy-Propyl Methacrylate (2-HPMA) serves as a reactive diluent in unsaturated polyesters and in automotive coatings.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is an acrylic ester monomer belonging to the methacrylate family.

2-Hydroxy-Propyl Methacrylate (2-HPMA) contains both a methacrylate functional group and a hydroxyl group, which makes it highly reactive and suitable for polymerization reactions.
Due to the presence of the hydroxyl functionality, 2-Hydroxy-Propyl Methacrylate (2-HPMA) can participate in cross-linking and copolymerization processes, making it valuable in the production of acrylic resins, coatings, adhesives, and UV-curable systems.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is commonly supplied as a clear, colorless to slightly yellow liquid and is soluble in water and many organic solvents.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is widely used as a reactive diluent, crosslinking monomer, and polymer modifier in various industrial applications including coatings, plastics, adhesives, and biomedical materials.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is an ester of Methacrylic Acid and is used as a raw material in polymer synthesis.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a functional hydrophobic-hydroxy monomer, consisting of a cyclic hydrophobic group with characteristic high reactivity of methacrylate.

2-Hydroxy-Propyl Methacrylate (2-HPMA) can form both homopolymers and copolymers.
Copolymers of 2-Hydroxy-Propyl Methacrylate (2-HPMA) can be prepared with (meth)acrylic acid and its salts, amides, and esters, as well as with (meth)acrylates, acrylonitrile, maleic acid esters, vinyl acetate, vinyl chloride, vinylidene chloride, styrene, butadiene, and other monomers.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is a hydroxy functional monomer used to make acrylic polyols and other hydrophilic polymers.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is an enoate ester that is the 1-methacryloyl derivative of propane-1,2-diol.
2-Hydroxy-Propyl Methacrylate (2-HPMA) has a role as a polymerisation monomer.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is functionally related to a propane-1,2-diol and a methacrylic acid.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is crystals or white crystalline solid.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a clear, colourless liquid with a characteristic odour.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is an ester of methacrylic acid.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is relatively non-volatile, non-toxic and non-yellowing.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is compared to HEMA is more suitable when a better water resistance is required, together with a better shrinkage resistance.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a methacrylate monomer derived from methacrylic acid.

2-Hydroxy-Propyl Methacrylate (2-HPMA) features a hydroxyl group attached to a propyl chain, which is connected to a methacrylate ester.
This structure gives 2-Hydroxy-Propyl Methacrylate (2-HPMA) dual functionalities: the methacrylate end is well-suited for free-radical polymerization, while the hydroxyl group enhances hydrophilicity and allows for further chemical modifications.

These characteristics provide scientists and engineers with an array of possibilities to design polymers with tailored properties.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is typically available as a colorless, viscous liquid with a mild odor.

2-Hydroxy-Propyl Methacrylate (2-HPMA) exhibits good solubility in water and many organic solvents, which enhances its utility in diverse applications, from coatings to biomedical devices.

With a boiling point of approximately 210°C and a density of 1.06 g/cm³, 2-Hydroxy-Propyl Methacrylate (2-HPMA) is relatively easy to handle under standard laboratory conditions, making it an ideal candidate for both academic and industrial research.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is non-toxic and non-yellowing.

USES and APPLICATIONS of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used extensively in the production of acrylic polyols for automotive OEM and refinish coatings as well as industrial coatings.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is also used as a co-monomer in styrene based unsaturated polyesters, PMMA based acrylic resins and vinyl ester formulations in anchor bolts and chemical fixings.

2-Hydroxy-Propyl Methacrylate (2-HPMA) may also be used in the production of emulsion polymers in combination with other commodity methacrylates and acrylates, notably for textile coatings and textile sizes.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is particularly useful as a hydrophobic hydroxy monomer in the production of vacuum impregnation sealants for cast aluminium components.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is also extensively used in the production of flexible, UV curable photopolymer printing plates.
2-Hydroxy-Propyl Methacrylate (2-HPMA)’s robust and adaptable nature has seen it integrated into several key industrial sectors.
In coatings and adhesives, 2-Hydroxy-Propyl Methacrylate (2-HPMA) is widely utilized to enhance durability and flexibility, especially in environments requiring superior weather and UV resistance.

The hydrophilic nature of 2-Hydroxy-Propyl Methacrylate (2-HPMA)-modified polymers also makes them excellent candidates for applications in the medical and pharmaceutical industries, where 2-Hydroxy-Propyl Methacrylate (2-HPMA) is a preferred choice in the production of hydrogels, dental materials, and contact lenses due to its excellent biocompatibility.

Furthermore, 2-Hydroxy-Propyl Methacrylate (2-HPMA)'s reactivity and functional groups are exploited in the creation of specialty polymers that are designed for high-performance uses.
These polymers are integral in the manufacture of sophisticated membranes, waterborne paints, and even 3D-printing materials, where precise control over mechanical and thermal properties is necessary.

The ability to create polymers that respond to environmental stimuli or exhibit self-healing properties is a testament to 2-Hydroxy-Propyl Methacrylate (2-HPMA)’s versatility in contemporary material science.
One of the most promising avenues for 2-Hydroxy-Propyl Methacrylate (2-HPMA) is its role in biomedical research, particularly in the development of drug delivery systems.

By incorporating 2-Hydroxy-Propyl Methacrylate (2-HPMA) into polymeric drug carriers, researchers have managed to achieve improved drug solubility, stability, and release kinetics.
These carriers often form hydrogels that can encapsulate pharmaceuticals and deliver them in a controlled manner, responding to specific physiological conditions such as pH or temperature changes.

In cancer therapy, for example, 2-Hydroxy-Propyl Methacrylate (2-HPMA)-based copolymers have shown promise in targeting tumors with increased specificity, minimizing side effects associated with traditional chemotherapy.
This is possible due to 2-Hydroxy-Propyl Methacrylate (2-HPMA)'s ability to form block copolymers that can be modified with targeting ligands or stimuli-responsive elements.

These innovations demonstrate 2-Hydroxy-Propyl Methacrylate (2-HPMA)’s crucial role in the ongoing evolution of smart materials within the medical field.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used for experimental / research use only.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is used in the manufacture of acrylic polymers for adhesives, inks, and coatings for automotive, appliance and metal applications.
The added hydroxyl groups improve adhesion to surfaces, incorporate cross-link sites, and impart corrosion, fogging, and abrasion resistance.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is a reactive monomer and functional intermediate widely used to synthesize water-compatible polyacrylates and hydrogel-forming polymers.
In practice, 2-Hydroxy-Propyl Methacrylate (2-HPMA) serves as a reactive diluent and hydroxyl-functional monomer for UV-curable coatings and inks, enabling improved crosslinking and surface adhesion.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is also employed in adhesive formulations and specialty resins where the pendant hydroxyl group allows post-polymerization modification.
Additionally, 2-Hydroxy-Propyl Methacrylate (2-HPMA) participates in hydrogel materials and polymer networks with swelling properties, and can be used as a modifier in resin systems to introduce hydroxyl functionality for coatings and related applications.

2-Hydroxy-Propyl Methacrylate (2-HPMA) used in the preparation of solid and emulsion polymers, acrylic dispersions in combination with other (meth) acrylates, which are used in various industries, especially for textile coatings and dressings.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is widely used in the production of acrylic polyols for automotive components, refurbishment coatings, and industrial coatings.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is also used as a comonomer in styrene-based unsaturated polyesters, PMMA-based acrylic resins, and vinyl ester formulations in anchor bolts and chemical anchors.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is particularly useful as a hydrophobic hydroxy monomer in the manufacture of sealants for vacuum impregnation of cast aluminum components.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is also widely used in the production of flexible UV-curable photopolymer printing plates.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a functional monomer for the preparation of hot solid acrylic coatings, styrene-butadiene latex modifiers, acrylic modified polyurethane coating ,water-soluble plating coatings , adhesives ,textile finishing agent ,paper coating , photosensitive paint and polyurethane vinyl resin modified agent.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is mainly used in the manufacture are active groups of hydroxyl acrylic resin.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used in reactive diluent and cross-linking agent in the UV curing system.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used in the preparation of solid and emulsion polymers, acrylic dispersions in conjunction with other (meth)acrylates, and finds applications in various industries, particularly in textile coatings and garments.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is used as a comonomer in the production of acrylic rollers for automotive components, maintenance coatings, and industrial coatings,
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used as a comonomer in styrene-based unsaturated polyesters, PMMA-based acrylic resins, and vinyl ester formulations for chemical anchors and chemical fasteners,

2-Hydroxy-Propyl Methacrylate (2-HPMA) is used as a hydrophobic hydroxy monomer in vacuum impregnation adhesives for cast aluminum components.
2-Hydroxy-Propyl Methacrylate (2-HPMA) used in the preparation of solid and emulsion polymers, acrylic dispersions in combination with other (meth) acrylates, which are used in various industries, especially for textile coatings and dressings.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is widely used in the production of acrylic polyols for automotive components, refurbishment coatings, and industrial coatings.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is also used as a comonomer in styrene-based unsaturated polyesters, PMMA-based acrylic resins, and vinyl ester formulations in anchor bolts and chemical anchors.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is particularly useful as a hydrophobic hydroxy monomer in the manufacture of sealants for vacuum impregnation of cast aluminum components.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is also widely used in the production of flexible UV-curable photopolymer printing plates.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is also used in textile treatments, where it improves wear resistance and water repellency of fabrics.

Additional applications of 2-Hydroxy-Propyl Methacrylate (2-HPMA) include medical adhesives, dental materials, photosensitive imaging materials, lubricant additives, and polymer modification processes.
2-Hydroxy-Propyl Methacrylate (2-HPMA) has several technical characteristics that make it useful in polymer chemistry and industrial formulations.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is a reactive monomer with high polymerization activity and good compatibility with other acrylic and methacrylate monomers.
The presence of a hydroxyl group enables strong adhesion and improved bonding to different substrates.

2-Hydroxy-Propyl Methacrylate (2-HPMA) demonstrates good solubility in both water and organic solvents, which allows it to be easily incorporated into coating, adhesive, and resin formulations.
2-Hydroxy-Propyl Methacrylate (2-HPMA) also provides improved mechanical properties and flexibility in polymers while maintaining chemical stability during processing.

2-Hydroxy-Propyl Methacrylate (2-HPMA) provides several benefits when used in polymer and coating systems.
2-Hydroxy-Propyl Methacrylate (2-HPMA) enhances cross-link density in resins, which improves mechanical strength and durability.
The hydroxyl functionality promotes adhesion and bonding between polymers and substrates.

2-Hydroxy-Propyl Methacrylate (2-HPMA) also contributes to improved chemical resistance, weather resistance, and flexibility in coatings and polymer materials.
Additionally, 2-Hydroxy-Propyl Methacrylate (2-HPMA) functions effectively as a reactive diluent in radiation-curable systems, helping reduce viscosity while maintaining polymer reactivity.

These properties make 2-Hydroxy-Propyl Methacrylate (2-HPMA) valuable in high-performance coatings, adhesives, and polymer formulations.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is widely used in many industrial sectors due to its polymerization capability and reactive hydroxyl group.

In the coatings industry, 2-Hydroxy-Propyl Methacrylate (2-HPMA) is used in automotive coatings, architectural coatings, and industrial coatings, where it helps improve durability, adhesion, and chemical resistance.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is also used as a reactive diluent in UV-curable coatings and radiation-curing systems to control viscosity and improve curing efficiency.

In adhesives and sealants, 2-Hydroxy-Propyl Methacrylate (2-HPMA) acts as a crosslinking monomer that enhances bonding strength and mechanical properties.
In plastics and rubber processing, it can function as a modifier that improves flexibility and durability.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is used monomer for acrylic resins, nonwoven fabric binders, detergent lubricating-oil additives.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a functional monomer for the preparation of hot solid acrylic coatings, styrene-butadiene latex modifiers, acrylic modified polyurethane coating, water-soluble plating coatings, adhesives, textile finishing agent, paper coating, photosensitive paint and polyurethane vinyl resin modified agent.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is mainly used in the manufacture are active groups of hydroxyl acrylic resin.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used in the preparation of solid and emulsion polymers, acrylic dispersions in combination with other (meth) acrylates, which are used in various industries, especially for textile coatings and dressings.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is mainly used for hot curing acrylic coating, UV-curable acrylic materials, photosensitive coating, water soluble plating coating, adhesive, textile treatment agent, ester polymer, modifier polymer, and stem acid water reducing agent, etc.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used in reactive diluent and cross-linking agent in the UV curing system.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is used in the manufacture of acrylic polymers for adhesives, printing inks, coatings and metal applications.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is also used as reactive diluent and alternative to styrene in unsatured polyester (UPR).

-2-Hydroxy-Propyl Methacrylate (2-HPMA) used in Ink Industry:
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used as a component in UV-curable resins for inks, where its reactive nature allows for rapid curing under ultraviolet light.
This results in inks with excellent adhesion, durability, and resistance to various environmental factors, making them suitable for a wide range of applications.

-2-Hydroxy-Propyl Methacrylate (2-HPMA) used in Dental Industry:
2-Hydroxy-Propyl Methacrylate (2-HPMA) is used as a monomer in dental composites and sealants for its ability to enhance the mechanical properties and durability of these materials.
2-Hydroxy-Propyl Methacrylate (2-HPMA)'s reactive hydroxyl groups allow for effective cross-linking, leading to improved strength and stability in dental applications.

KEY DETAILS AND APPLICATIONS of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
*Chemical Properties:
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a hydroxy-functional monomer that copolymerizes with various monomers (styrene, acrylic acid, etc.) to enhance cross-linking.

*Key Uses:
2-Hydroxy-Propyl Methacrylate (2-HPMA) is widely utilized in UV-curable coatings, printing plates, industrial coatings, water-soluble, and solvent-based acrylic resins.

*Industry Applications:
Essential in automotive finishes, textile treating, adhesives, paper coatings, and dental materials.

*Performance Benefits:
2-Hydroxy-Propyl Methacrylate (2-HPMA) improves flexibility, corrosion resistance, and adhesion to surfaces.
Safety: While used in nail products, 2-Hydroxy-Propyl Methacrylate (2-HPMA) requires careful handling to avoid skin sensitization.

2-HYDROXY-PROPYL METHACRYLATE (2-HPMA): A VERSATILE MONOMER IN MODERN CHEMISTRY
2-Hydroxy-Propyl Methacrylate (2-HPMA) has gained significant attention within the realm of polymer chemistry.
2-Hydroxy-Propyl Methacrylate (2-HPMA) is increasingly becoming a staple in a variety of industrial and research applications.
2-Hydroxy-Propyl Methacrylate (2-HPMA)’s unique properties, such as its reactive methacrylate group and hydrophilic hydroxy group, make it an indispensable component in the synthesis of polymers and copolymers, serving as a bridge between organic chemistry and material science.

KEY PROPERTIES AND REACTIVITY of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
The primary allure of 2-Hydroxy-Propyl Methacrylate (2-HPMA) lies in its functional versatility.
The methacrylate moiety allows 2-Hydroxy-Propyl Methacrylate (2-HPMA) to undergo free-radical polymerization, which is a common method for producing polymers with a variety of structures and properties.

By participating in copolymerization reactions with other monomers—such as styrene, acrylates, or vinyl compounds—2-Hydroxy-Propyl Methacrylate (2-HPMA) imparts enhanced adhesive strength, improved thermal stability, and greater mechanical flexibility to the resultant polymers.
Additionally, the hydroxyl group present in 2-Hydroxy-Propyl Methacrylate (2-HPMA) serves as a reactive site for subsequent chemical reactions, such as esterification, etherification, or cross-linking.

This enables the creation of complex polymer networks or grafted structures, which are crucial for specialized applications.
The inclusion of the hydroxyl group also improves compatibility with a range of substrates, thereby extending 2-Hydroxy-Propyl Methacrylate (2-HPMA)’s application scope into advanced fields like drug delivery systems, where biocompatibility and hydrophilicity are essential.

PROPERTIES of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
*Chemical resistance
*Hydrolytic stability
*Hydrophobicity
*Flexibility
*Adhesion
*Shock resistance
*Weather resistance

CHEMICAL PROPERTIES of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
2-Hydroxy-Propyl Methacrylate (2-HPMA) is a reactive methacrylate monomer containing both vinyl and hydroxyl functional groups.
The methacrylate double bond readily participates in free-radical polymerization reactions, allowing 2-Hydroxy-Propyl Methacrylate (2-HPMA) to form homopolymers or copolymers with other acrylic monomers.

The hydroxyl group provides additional reactivity and enables cross-linking reactions with isocyanates, epoxies, or other reactive compounds.
2-Hydroxy-Propyl Methacrylate (2-HPMA) exhibits good compatibility with acrylic resins and polymer matrices.

2-Hydroxy-Propyl Methacrylate (2-HPMA) is often stabilized with small amounts of polymerization inhibitors such as MEHQ (hydroquinone monomethyl ether) to prevent premature polymerization during storage.
Due to its chemical structure, 2-Hydroxy-Propyl Methacrylate (2-HPMA) improves adhesion, flexibility, and chemical resistance in polymer systems.

2-HYDROXY-PROPYL METHACRYLATE (2-HPMA) IS APPLIED IN THE PRODUCTION OF;
*Automotive coatings
*Architectural coatings
*Industrial coatings
*Plastics
*Hygiene products
*Adhesives and sealants
*Textile finishes
*Modifications
*Photosensitive materials
*Additives for oil production and transportation

PHYSICAL and CHEMICAL PROPERTIES of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
Formula: C7H12O3
Formula Weight: 144.17
CAS #: 27813-02-1
Boiling Point: 70°C/1mmHg
Specific Gravity @25°C: 1.028
Solubility in Water: 13%
Appearance: White odorless crystals
Physical state: solid
Color: No data available
Odor: No data available

Melting point/freezing point:
Melting point/range: 70 °C
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: No data available
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available

Appearance: Clear liquid, free of particles
Water content, % (mass): 0.1 max
Inhibitor (MEHQ) content, ppm (mass): 200 - 300
Acid number, mgKOH/g: 1.0 max.
Colour number, Pt/Co: 10 max
Assay, % (mass): 97.0 min
Diester (PGDMA), % (mass): 0.2 max
Molecular weight (av), g/mol: 144
PSA: 46.53000
XLogP3: 0.48650
Appearance: Crystals or white crystalline solid.

Density: 1.066 g/cm3 @ Temp: 25 °C
Melting Point: -89 °C
Boiling Point: 96 °C
Flash Point: 206 °F
Refractive Index: 1.447
Water Solubility: less than 1 mg/mL at 73° F
Storage Conditions: 0-6ºC
Vapor Pressure: 0.05 mm Hg ( 20 °C)
Vapor Density: >1 (vs air)Odor: Slight acrylic odor

Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: ca.1,002 g/cm3
Relative density: No data available
Relative vapor density: No data available

Particl characteristics: No data available
Explosive properties: No data available
Oxidizing properties: No data available
Other safety information: No data available
Molecular Weight: 144.17 g/mol
XLogP3: 1
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 4
Exact Mass: 144.078644241 g/mol

Monoisotopic Mass: 144.078644241 g/mol
Topological Polar Surface Area: 46.5Å²
Heavy Atom Count: 10
Formal Charge: 0
Complexity: 140
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0

Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Empirical Formula: C7H12O3
CAS No.: 27813-02-1
Color: max.30 (Pt-Co)
Stabilization: 200±20ppm MEHQ
Appearance: Clear, colorless liquid
Molecular weight: 144.7 g/mol
Density: 1.066 g/cm3 (25ºC)
Refractive index: 1.447(25ºC)

Boiling point: 92ºC
Flashpoint: 96ºC
Solubility: Soluble in : Organic Solvent, Water
Melting point: -58°C
Boiling point: 57 °C/0.5 mmHg (lit.)
Density: 1.066 g/mL at 25 °C (lit.)
vapor density: >1 (vs air)
vapor pressure: 0.05 mm Hg ( 20 °C)
refractive index: n20/D 1.447(lit.)
Flash point: 206 °F

storage temp.: 2-8°C
solubility: 107g/l
form: Liquid
color: Clear
Specific Gravity: 1.066
PH: 6 (50g/l, H2O, 20℃)
Viscosity: 8.88mm2/s
Water Solubility: Soluble in water.

BRN: 1752228
InChIKey: GNSFRPWPOGYVLO-UHFFFAOYSA-N
LogP: 0.97 at 20℃
Indirect Additives used in Food Contact Substances: HYDROXYPROPYL METHACRYLATE
FDA 21 CFR: 175.105
CAS DataBase Reference: 27813-02-1(CAS DataBase Reference)
FDA UNII: UKW89XAX2X
EPA Substance Registry System: Hydroxypropyl methacrylate (27813-02-1)

XLogP3: 1
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 4
Exact Mass: 144.078644241 Da
Monoisotopic Mass: 144.078644241 Da
Topological Polar Surface Area: 46.5 Å²
Heavy Atom Count: 10
Formal Charge: 0
Complexity: 140
Isotope Atom Count: 0

Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Other (deleted CASRN): 122413-04-1
ECHA EINECS - REACH Pre-Reg: 248-666-3
FDA UNII: UKW89XAX2X

Nikkaji Web: J101.364E
Beilstein Number: 1752228
XlogP3: 1.30 (est)
Molecular Weight: 144.17024000
Formula: C7 H12 O3
Appearance: colorless to pale yellow clear liquid (est)
Assay: 95.00 to 100.00 sum of isomers
Food Chemicals Codex Listed: No
Specific Gravity: 1.06600 @ 25.00 °C
Boiling Point: 218.76 °C @ 760.00 mm Hg (est)

Vapor Pressure: 0.026000 mmHg @ 25.00 °C (est)
Flash Point: 206.00 °F TCC (96.67 °C)
logP (o/w): 0.781 (est)
Soluble in: water, 3.863e+004 mg/L @ 25 °C (est)
Chemical Name: 2-Hydroxypropyl Methacrylate
CAS Number: 27813-02-1 (commonly used)
Alternative CAS Number: 923-26-2
EC Number (EINECS): 248-666-3
Molecular Formula: C7H12O3

Molecular Weight: 144.17 g/mol
Chemical Class: Methacrylate ester / Acrylic monomer
Appearance: Colorless to light yellow transparent liquid
Physical State: Liquid
Odor: Mild acrylic odor
Density: ~1.066 g/cm³ at 20–25 °C
Melting / Freezing Point: −58 °C
Boiling Point: ~218 °C (760 mmHg)
Flash Point: ~104 °C

Vapor Pressure: ~0.05 mmHg at 20 °C
Refractive Index: ~1.447
Viscosity: ~8.9 mPa·s (20 °C)
Solubility: Soluble in water and many organic solvents
pH: ~6 (50 g/L aqueous solution)
LogP: ~0.85–0.97
Exact Mass: 144.0786
Surface Polarity (PSA): ~46.53 Å²
Molecular Weight: 144.17 g/mol

Product Name: Hydroxypropyl methacrylate
CAS No.: 27813-02-1
Molecular Formula: C7H12O3
InChIKeys: VHSHLMUCYSAUQU-UHFFFAOYSA-N
Molecular Weight: 144.16800
Exact Mass: 144.07900
EC Number: 213-090-3
HScode: 2916140000
Categories: Organic Reagents
PSA: 46.53000

XLogP3: 0.48650
Appearance: Crystals or white crystalline solid.
Density: 1.066 g/cm3 @ Temp: 25 °C
Melting Point: -89 °C
Boiling Point: 96 °C
Flash Point: 206 °F
Refractive Index: 1.447
Water Solubility: less than 1 mg/mL at 73° F
Storage Conditions: 0-6 ºC

Vapor Pressure: 0.05 mm Hg (20 °C)
Vapor Density: >1 (vs air)
Odor: Slight acrylic odor
CAS Number: 27813-02-1
MDL number: MFCD00051317
UNSPSC Code: 12162002
PubChem Substance ID: 24856280
NACRES: NA.23

Beilstein/REAXYS Number: 1752228
Physical state: liquid
Color: No data available
Odor: No data available
Melting point/range: -60 °C
Boiling point/boiling range: 205 - 209 °C
Flammability: No data available
Upper explosion limit / Upper flammability limit: No data available
Lower explosion limit / Lower flammability limit: No data available

Flash point: 95 °C
Method: closed cup
Autoignition temperature: 355 °C
Decomposition temperature: No data available
pH: No data available
Viscosity, dynamic: No data available
Viscosity, kinematic: No data available
Flow time: No data available
Water solubility: No data available

Partition coefficient: noctanol/water: No data available
Vapor pressure: 0,066 hPa (20 °C)
Relative density: No data available
Density: 1,066 g/cm3 (25 °C)
Method: lit.
Relative vapour density: No data available
Other information
Explosives: Not classified as explosive.
Oxidizing properties: none

Burning rate: No data available
Evaporation rate: No data available
Molecular weight: 144,17 g/mol
Melting point: -58 °C
Boiling point: 57 °C/0.5 mmHg (lit.)
Density: 1.066 g/mL at 25 °C (lit.)
Vapor density: >1 (vs air)
Vapor pressure: 0.05 mm Hg (20 °C)
Refractive index: n20/D 1.447 (lit.)

Fp: 206 °F
Storage temp: 2-8 °C
Solubility: 107 g/l
Form: Liquid
Color: Clear
Specific Gravity: 1.066
PH: 6 (50 g/l, H2O, 20 ℃)
Water Solubility: Soluble in water.
BRN: 1752228
InChIKey: GNSFRPWPOGYVLO-UHFFFAOYSA-N

LogP: 0.97 at 20 ℃
CAS DataBase Reference: 27813-02-1 (CAS DataBase Reference)
EPA Substance Registry System: Hydroxypropyl methacrylate (27813-02-1)
CBNumber: CB9299748
Molecular Formula: C7H12O3
Molecular Weight: 144.17
MDL Number: MFCD00004536
MOL File: 27813-02-1.mol
Melting Point: -58 °C

Boiling Point: 57 °C/0.5 mmHg (lit.)
Density: 1.066 g/mL at 25 °C (lit.)
Vapor Density: >1 (vs air)
Vapor Pressure: 0.05 mm Hg (20 °C)
Refractive Index: n20/D 1.447 (lit.)
Flash Point: 206 °F
Storage Temp: 2-8 °C
Solubility: 107 g/l
Form: Liquid

Specific Gravity: 1.066
Color: Clear
PH: 6 (50 g/l, H2O, 20 ℃)
Viscosity: 8.88 mm2/s
Water Solubility: Soluble in water.
BRN: 1752228
Cosmetics Ingredients Functions: FILM FORMING
InChIKey: GNSFRPWPOGYVLO-UHFFFAOYSA-N
LogP: 0.97 at 20 ℃

CAS DataBase Reference: 27813-02-1 (CAS DataBase Reference)
Indirect Additives Used in Food Contact Substances: HYDROXYPROPYL METHACRYLATE
FDA 21 CFR: 175.105
FDA UNII: UKW89XAX2X
EPA Substance Registry System: Hydroxypropyl methacrylate (27813-02-1)
UNSPSC Code: 12162002
NACRES: NA.23
Appearance: clear
Physical Form: liquid

Odor: -
Molecular Weight: 144.17 g/mol
Polymer Tg: -
Tg: -
Density: 1,029 g/cm3 at 20 °C
Boiling Point: 209 °C (5 mmHg)
Freezing Point: -58 °C
Flash Point: 104 °C
Melting Point: -58 °C
Viscosity: 8.9 mPa · s at 20 °C
Vapor Point: 0.05 mm Hg at 20 °C

FIRST AID MEASURES of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
-Description of first-aid measures:
*General advice:
Consult a physician.
*If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
*In case of skin contact:
Wash off with soap and plenty of water.
Consult a physician.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Rinse mouth with water.
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available

ACCIDENTAL RELEASE MEASURES of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Sweep up and shovel.
Keep in suitable, closed containers for disposal.

FIRE FIGHTING MEASURES of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available

EXPOSURE CONTROLS/PERSONAL PROTECTION of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Respiratory protection:
Respiratory protection is not required.
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
-Precautions for safe handling:
*Hygiene measures:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
*Storage stability:
Recommended storage temperature: 2 - 8 °C
Handle under nitrogen, protect from moisture.
Store under nitrogen.
Heat- and airsensitive.
Moisture sensitive.

STABILITY and REACTIVITY of 2-HYDROXY-PROPYL METHACRYLATE (2-HPMA):
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available