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1,3 adamantanediol diacrylate 81665 82 9 structure

1,3-Adamantanediol diacrylate

1,3-Adamantanediol diacrylate, identified by CAS number 81665-82-9, is a specialized bifunctional monomer characterized by its rigid, cage-like adamantane core substituted with two reactive acrylate groups. This unique molecular architecture imparts exceptional thermal stability and mechanical strength to the resulting polymers. As a high-performance cross-linking agent, it is valued for its ability to enhance the physical

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Methyl E 3 2 Amino 3 Fluorophenyl Acrylate 690664 20 1 Structure

Methyl (E)-3-(2-amino-3-fluorophenyl)acrylate

Methyl (E)-3-(2-amino-3-fluorophenyl)acrylate, identified by CAS number 690664-20-1, is a specialized organic building block characterized by its cinnamate backbone, an ortho-amino group, and a fluorine substituent on the aromatic ring. This compound serves as a versatile intermediate in complex molecular assembly, offering multiple reactive sites for further chemical transformation. Its structural configuration, particularly the (E)-stereochemistry of

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Methylhydrosiloxane Dimethylsiloxane%20copolymer 69013 23 6 Structure 1024x768

Methylhydrosiloxane-dimethylsiloxane copolymer, hydride terminated

Methylhydrosiloxane-dimethylsiloxane copolymer, hydride terminated (CAS 69013-23-6), is a versatile reactive silicone fluid characterized by the presence of active silicon-hydrogen (Si-H) bonds both along the polymer backbone and at the chain ends. This specific molecular architecture combines the stability and flexibility of dimethylsiloxane units with the high reactivity of methylhydrosiloxane units. As a clear, low-to-medium viscosity

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2 Ethylhexyl Methacrylate 688 84 6 Structure

2-Ethylhexyl Methacrylate

2-Ethylhexyl Methacrylate, identified by CAS number 688-84-6, is a versatile methacrylate monomer characterized by its long-chain alkyl group. As a clear, colorless liquid with a characteristic odor, it serves as a critical building block in the synthesis of various acrylic polymers and copolymers. Its primary chemical advantage lies in its ability to impart internal plasticization

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Tetrabromobisphenol A Epoxy Resin Intermediate 68928 70 1 Structure

Tetrabromobisphenol A Epoxy Resin Intermediate

Tetrabromobisphenol A Epoxy Resin Intermediate, identified by CAS 68928-70-1, is a specialized brominated oligomeric compound primarily utilized in the synthesis of high-performance flame-retardant materials. This chemical intermediate is characterized by its significant bromine content and reactive epoxy groups, which allow it to integrate seamlessly into various polymer matrices. Its chemical structure provides a robust foundation

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Polyether Modified Silicone Oil 68937 54 2 Structure 1024x768

polyether-modified silicone oil

Polyether-modified silicone oil, identified by CAS 68937-54-2, is a versatile non-ionic surfactant belonging to the class of organosilicon compounds. It is synthesized by grafting polyether chains, typically ethylene oxide or propylene oxide, onto a polydimethylsiloxane backbone. This unique molecular architecture combines the low surface tension and lubricity of silicone with the hydrophilicity and solubility of

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oxidized polyethylene 68441 17 8 structure

Oxidized Polyethylene

Oxidized Polyethylene (OPE), identified by CAS 68441-17-8, is a functionalized polymer produced through the controlled oxidation of polyethylene. This chemical modification introduces polar functional groups, including carboxylic acids and esters, onto the hydrocarbon chain. These groups significantly improve the polymer’s emulsifiability and its compatibility with polar materials, distinguishing it from traditional non-polar polyethylene waxes. Technically,

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3 3 3 Trifluoropropyl Acrylate 65605 70 1 Structure

3,3,3-Trifluoropropyl acrylate

3,3,3-Trifluoropropyl acrylate (CAS 65605-70-1) is a specialized fluorinated monomer characterized by the presence of a trifluoromethyl group attached to a propyl chain, which is further esterified with acrylic acid. This chemical structure imparts unique physicochemical properties to the resulting polymers, including enhanced thermal stability, low surface energy, and improved resistance to chemical degradation. As a

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diphenylsiloxane dimethylsiloxane copolymer 68083 14 7 structure

diphenylsiloxane-dimethylsiloxane copolymer

Diphenylsiloxane-dimethylsiloxane copolymer, identified by CAS 68083-14-7, is a versatile phenyl-modified silicone fluid characterized by the incorporation of phenyl groups into a polydimethylsiloxane backbone. This chemical modification significantly enhances the polymer’s thermal stability and oxidative resistance compared to standard dimethyl silicone oils. It exhibits a high refractive index and remains stable across a wide temperature range,

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3 Diethoxy Methyl Silyl Propyl Methacrylate MPTMS Me 65100 04 1 Structure

3‑(Diethoxy(methyl)silyl)propyl Methacrylate (MPTMS‑Me)

3-(Diethoxy(methyl)silyl)propyl Methacrylate, identified by CAS 65100-04-1, is a versatile organosilane monomer featuring both a reactive methacrylate group and a hydrolyzable diethoxymethylsilyl moiety. This bifunctional structure allows the molecule to bridge the gap between organic polymers and inorganic substrates, facilitating the development of high-performance composite materials. As a clear, colorless liquid, it is valued for its

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light stabilizer 622 65447 77 0 structure

Light Stabilizer 622

Light Stabilizer 622, identified by CAS 65447-77-0, is a high-molecular-weight polymeric hindered amine light stabilizer (HALS). Chemically, it is a polyester composed of succinic acid and 4-hydroxy-2,2,6,6-tetramethyl-1-piperidineethanol. This specific structural composition grants the material exceptional thermal stability and low volatility, making it a preferred choice for applications requiring long-term durability under intense ultraviolet exposure. Its

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Styrenated Phenol 61788 44 1 Structure

Styrenated phenol

Styrenated phenol, identified by CAS number 61788-44-1, is a versatile chemical intermediate and antioxidant widely utilized across various industrial sectors. Chemically, it exists as a mixture of mono-, di-, and tri-styrenated phenols, typically appearing as a clear to light yellow viscous liquid. Its unique molecular structure, combining the aromatic properties of phenol with styrene substituents,

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M Tolyl Isocyanate 621 29 4 Structure

m‑Tolyl Isocyanate

m-Tolyl Isocyanate, identified by CAS number 621-29-4, is a highly reactive organic compound belonging to the isocyanate family. Also known as 3-methylphenyl isocyanate, this chemical appears as a colorless to pale yellow liquid with a characteristic pungent odor. It is characterized by the presence of a reactive isocyanate group attached to a meta-substituted toluene ring,

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P Tolyl Isocyanate 622 58 2 Structure

p‑Tolyl Isocyanate

p-Tolyl isocyanate, identified by CAS number 622-58-2, is a versatile aromatic isocyanate characterized by its reactive isocyanate group attached to a para-methyl substituted benzene ring. Typically appearing as a colorless to slightly yellow liquid or low-melting crystalline solid, this compound is a critical building block in organic chemistry. Its high reactivity toward nucleophiles makes it

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9 9 Dimethyl 10H Acridine Acridan 6267 02 3 Structure

9,9‑Dimethyl‑10H‑acridine (Acridan)

9,9-Dimethyl-10H-acridine, commonly known as a substituted acridan, is a specialized organic building block characterized by its rigid heterocyclic structure. With the CAS registry number 6267-02-3, this compound features a central acridine framework where the 9-position is substituted with two methyl groups, significantly influencing its conformational and electronic properties. It typically appears as a white to

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2 2 Naphthyloxy Ethyl Acrylate 64022 15 7 Structure

2‑(2‑Naphthyloxy)ethyl Acrylate

2-(2-Naphthyloxy)ethyl Acrylate, identified by CAS number 64022-15-7, is a specialized aromatic monofunctional monomer characterized by its naphthalene ring structure. This chemical exhibits a high refractive index and low volatility, making it a valuable component in the formulation of high-performance polymers and coatings. Its molecular architecture provides a balance of rigidity from the naphthyl group and

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