Beschreibung
ACMO Monomer / 4-Acryloylmorpholin cas 5117-12-4
Artikel | Spezifikation |
Erscheinungsbild | Farblose oder hellgelbe klare Flüssigkeit |
Assay | ≥98.0% |
Farbe | ≤50APHA |
Viskosität | ≤12cps(25℃) |
Luftfeuchtigkeit | ≤0,3% |
ACMO Monomer / 4-Acryloylmorpholin Anwendung
1. ACMO, as a heat-resistant functional monomer of great importance in the field of materials science, exhibits a number of remarkable qualities. In terms of skin irritation, its P.I.I. value is as low as 0.5, which means that its potential irritation to human skin is minimal, greatly guaranteeing its safety in relevant application scenarios. It is also worth mentioning that ACMO has a very low vapor pressure, which makes it virtually odorless during use, effectively avoiding the impact of bad odors from volatiles on the environment and the user, thus broadening its application scope, for example, in the field of interior decoration materials or personal care products that are sensitive to odors.
2. In practical applications, ACMO’s low viscosity combined with its fast curing advantage makes it an indispensable active diluent in UV-curable resins. Take the coating of electronic products as an example, ACMO can be quickly and uniformly dispersed in the resin system, curing rapidly under UV irradiation to form a tough and stable protective film, effectively improving the wear and corrosion resistance of the product, and meeting the demand for thin, light and durable coatings for electronic products.
3. In-depth exploration of the homopolymer of ACMO, its good dilution and solubility make it can be perfectly adapted with a variety of solvents. This property plays a key role in the coatings and inks industries. For example, in the development of waterborne coatings, ACMO homopolymers help to disperse pigments and ensure good leveling and spreading properties, which improves the quality of the coatings and the efficiency of their application.
4. ACMO shows excellent compatibility with oligomers, functional propionates and tree cells. In the preparation of composite materials, this good compatibility enables ACMO to be closely combined with other components to synergize their respective advantages and significantly improve the comprehensive performance of the materials. For example, in high-performance fiber-reinforced composites, the addition of ACMO can optimize the interfacial bonding between resin matrix and fibers, and enhance the mechanical properties and durability of the materials.
5. In the process of polymerization reaction, compared with most of the propionic acid monomers, the curing speed of ACMO has obvious advantages. From the point of view of chemical reaction kinetics, the molecular structure and reactive groups of ACMO enable it to react more efficiently with other monomers during the polymerization process to form a stable polymer network. This property is of great value in rapid prototyping processes. For example, in the field of 3D printing, resin materials using ACMO as one of the monomers can achieve rapid layer-by-layer curing, improving printing efficiency and model accuracy.
6. ACMO-modified UV and EB curing resins exhibit excellent resistance to moisture absorption, acids and alkalis, and solvents. In the coating of chemical storage containers, these resins are effective in resisting acid and alkali solutions and organic solvents, preventing rust and corrosion, extending the life of the container, and reducing maintenance costs and safety risks for organizations.
The nitrogen radical in the ACMO molecule contains a unique chemical activity that effectively inhibits oxygen-induced polymerization reactions. This property is critical in scenarios where the precision of the polymerization reaction is critical, such as in the preparation of optical materials, where the presence of ACMO ensures that the polymerization reaction proceeds as expected, avoiding defects due to oxygen interference, thus ensuring high transparency and stability of the optical properties of the optical material.
ACMO Monomer / 4-Acryloylmorpholin Eigenschaften
1.wasserlösliches Monomer
2. schnelle Aushärtung
3. niedrige Viskosität
4. geringe Volatilität
5. geringere Reizung der Haut.
ACMO Monomer / 4-Acryloylmorpholin Verpackung und Versand
Verpackung: 25L oder 200L/Fass.
Lieferung: innerhalb von 5-7 Arbeitstagen.
ACMO Monomer / 4-Acryloylmorpholin Lagerung
An einem kühlen, trockenen Ort ohne direkte Sonneneinstrahlung aufbewahren.
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Polythiol/Polymercaptan | ||
DMES Monomer | Bis(2-mercaptoethyl)sulfid | 3570-55-6 |
DMPT Monomer | THIOCURE DMPT | 131538-00-6 |
PETMP-Monomer | 7575-23-7 | |
PM839 Monomer | Polyoxy(methyl-1,2-ethandiyl) | 72244-98-5 |
Monofunktionelles Monomer | ||
HEMA-Monomer | 2-Hydroxyethylmethacrylat | 868-77-9 |
HPMA-Monomer | 2-Hydroxypropylmethacrylat | 27813-02-1 |
THFA-Monomer | Tetrahydrofurfurylacrylat | 2399-48-6 |
HDCPA Monomer | Hydriertes Dicyclopentenylacrylat | 79637-74-4 |
DCPMA-Monomer | Dihydrodicyclopentadienylmethacrylat | 30798-39-1 |
DCPA Monomer | Dihydrodicyclopentadienyl-Acrylat | 12542-30-2 |
DCPEMA-Monomer | Dicyclopentenyloxyethylmethacrylat | 68586-19-6 |
DCPEOA-Monomer | Dicyclopentenyloxyethylacrylat | 65983-31-5 |
NP-4EA Monomer | (4) ethoxyliertes Nonylphenol | 50974-47-5 |
LA Monomer | Laurylacrylat / Dodecylacrylat | 2156-97-0 |
THFMA Monomer | Tetrahydrofurfurylmethacrylat | 2455-24-5 |
PHEA-Monomer | 2-PHENOXYETHYLACRYLAT | 48145-04-6 |
LMA Monomer | Laurylmethacrylat | 142-90-5 |
IDA Monomer | Isodecylacrylat | 1330-61-6 |
IBOMA Monomer | Isobornylmethacrylat | 7534-94-3 |
IBOA Monomer | Isobornylacrylat | 5888-33-5 |
EOEOEA Monomer | 2-(2-Ethoxyethoxy)ethylacrylat | 7328-17-8 |
Multifunktionelles Monomer | ||
DPHA Monomer | 29570-58-9 | |
DI-TMPTA Monomer | DI(TRIMETHYLOLPROPAN)TETRAACRYLAT | 94108-97-1 |
Acrylamid-Monomer | ||
ACMO Monomer | 4-Acryloylmorpholin | 5117-12-4 |
Difunktionelles Monomer | ||
PEGDMA-Monomer | Poly(ethylenglykol)dimethacrylat | 25852-47-5 |
TPGDA Monomer | Tripropylenglykol-Diacrylat | 42978-66-5 |
TEGDMA-Monomer | Triethylenglykol-Dimethacrylat | 109-16-0 |
PO2-NPGDA Monomer | Propoxylat-Neopentylenglykol-Diacrylat | 84170-74-1 |
PEGDA-Monomer | Polyethylenglykol-Diacrylat | 26570-48-9 |
PDDA-Monomer | Phthalat Diethylenglykol-Diacrylat | |
NPGDA Monomer | Neopentylglykol-Diacrylat | 2223-82-7 |
HDDA-Monomer | Hexamethylen-Diacrylat | 13048-33-4 |
EO4-BPADA Monomer | ETHOXYLIERTES (4) BISPHENOL-A-DIACRYLAT | 64401-02-1 |
EO10-BPADA Monomer | ETHOXYLIERTES (10) BISPHENOL-A-DIACRYLAT | 64401-02-1 |
EGDMA Monomer | Ethylenglykol-Dimethacrylat | 97-90-5 |
DPGDA-Monomer | Dipropylenglykol-Dienoat | 57472-68-1 |
Bis-GMA-Monomer | Bisphenol A Glycidylmethacrylat | 1565-94-2 |
Trifunktionelles Monomer | ||
TMPTMA Monomer | Trimethylolpropantrimethacrylat | 3290-92-4 |
TMPTA-Monomer | Trimethylolpropantriacrylat | 15625-89-5 |
PETA Monomer | 3524-68-3 | |
GPTA ( G3POTA ) Monomer | GLYCERIN-PROPOXYTRIACRYLAT | 52408-84-1 |
EO3-TMPTA Monomer | Ethoxyliertes Trimethylolpropantriacrylat | 28961-43-5 |
Photoresist Monomer | ||
IPAMA-Monomer | 2-Isopropyl-2-adamantylmethacrylat | 297156-50-4 |
ECPMA Monomer | 1-Ethylcyclopentylmethacrylat | 266308-58-1 |
ADAMA Monomer | 1-Adamantylmethacrylat | 16887-36-8 |
Methacrylat-Monomer | ||
TBAEMA Monomer | 2-(Tert-Butylamino)ethylmethacrylat | 3775-90-4 |
NBMA Monomer | n-Butylmethacrylat | 97-88-1 |
MEMA Monomer | 2-Methoxyethylmethacrylat | 6976-93-8 |
i-BMA Monomer | Isobutylmethacrylat | 97-86-9 |
EHMA Monomer | 2-Ethylhexylmethacrylat | 688-84-6 |
EGDMP-Monomer | Ethylenglykol-Bis(3-mercaptopropionat) | 22504-50-3 |
EEMA Monomer | 2-Ethoxyethyl-2-methylprop-2-enoat | 2370-63-0 |
DMAEMA Monomer | N,M-Dimethylaminoethylmethacrylat | 2867-47-2 |
DEAM Monomer | Diethylaminoethylmethacrylat | 105-16-8 |
CHMA Monomer | Cyclohexylmethacrylat | 101-43-9 |
BZMA-Monomer | Benzylmethacrylat | 2495-37-6 |
BDDMP-Monomer | 1,4-Butandiol Di(3-mercaptopropionat) | 92140-97-1 |
BDDMA-Monomer | 1,4-Butandioldimethacrylat | 2082-81-7 |
AMA Monomer | Allylmethacrylat | 96-05-9 |
AAEM Monomer | Acetylacetoxyethylmethacrylat | 21282-97-3 |
Acrylate Monomer | ||
IBA Monomer | Isobutyl-Acrylat | 106-63-8 |
EMA-Monomer | Ethylmethacrylat | 97-63-2 |
DMAEA Monomer | Dimethylaminoethylacrylat | 2439-35-2 |
DEAEA Monomer | 2-(Diethylamino)ethylprop-2-enoat | 2426-54-2 |
CHA Monomer | Cyclohexylprop-2-enoat | 3066-71-5 |
BZA Monomer | Benzylprop-2-enoat | 2495-35-4 |
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