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  • Trimethylchlorosilane (TMCS)  CAS :75-77-4

    Trimethylchlorosilane (TMCS) CAS :75-77-4

    Name: Chlorotrimethylsilane CAS number: 75-77-4 Molecular formula: C3H9ClSi Molecular weight: 108.64 EINECS number: 200-900-5 Mol file: 75-77-4.mol

  • Trimethylethoxysilane CAS :1825-62-3

    Trimethylethoxysilane CAS :1825-62-3

    Name: Ethoxytrimethylsilane CAS number: 1825-62-3 Molecular formula: C5H14OSi Molecular weight: 118.25 EINECS number: 217-370-6 Mol file: 1825-62-3.mol

  • Dimethyldimethoxysilane CAS1112-39-6 DMDMS

    Dimethyldimethoxysilane CAS1112-39-6 DMDMS

    Specification English name: Dimethyldimethoxysilane CAS number: 1112-39-6 Molecular formula: C4H12O2Si Molecular weight: 120.22 EINECS number: 214 189 4 Mol file: 1112-39-6.mol Applications As a structural control agent, chain extender, and filler treatment agent, it is widely used in the treatment of organic silica gel and white carbon black Purpose As a structural control agent, chain extender, and filler treatment agent, it is widely used in the treatment of organic silica gel and white carbon black. This product is used as a structural control agent and chain extender to improve mechanical processing performance, extend the storage time of rubber blends, and can replace hydroxyl silicone oil for use. Widely used in the treatment of organic silicone and white carbon black Purpose Dimethyldimethoxysilane is used as a structural control agent and chain extender to improve mechanical processing performance, extend the storage time of rubber blends, and can replace hydroxy silicone oil....

  • Iodotrimethylsilane CAS:16029-98-4 (TMIS)

    Iodotrimethylsilane CAS:16029-98-4 (TMIS)

    Properties of trimethyliodosilane Melting point<0 ° C Boiling point 106 ° C (lit.) Density 1.406 g/mL at 25 ° C (lit.) Refractive index n20/D 1.471 (lit.) Flash point − 25 ° F Storage conditions -20 ° C Solubility Reacts Form Liquid Specific gravity 1.47 Clear colors to reddish Water solubility reactions Sensitivity: Moisture&Light Sensitivity Hydrolysis sensitivity 8: Reacts quickly with moisture, water, protoc solvents BRN 1731136 Stability Sensitivity (Reactive) InchiKey CSRZQMIRAZTJOY-UHFFFFAOYSA-N CAS Database 16029-98-4 (CAS DataBase Reference) NIST Chemical Information Iodotrimethylsilane (16029-98-4) EPA Chemical Information Silane, iodotrimethyl - (16029-98-4)

  • Hexamethyldisilane CAS:1450-14-2 (HMD)

    Hexamethyldisilane CAS:1450-14-2 (HMD)

    Properties of Hexamethyldisilane Melting point 9-12 ° C (lit.) Boiling point 112-114 ° C (lit.) Density 0.715 g/mL at 25 ° C (lit.) Refractive index n20/D 1.422 (lit.) Flash point 29 ° F Storage conditions Store at<=20 ° C Sol common organic solvents; Insul H2O Form liquid Specific gravity 0.729 Colorless Insoluble in water Double in alcohol, ether and acetone Hydrolysis sensitivity 1: no significant reaction with acute systems BRN 1633463 Stability InchiKey NEXSMEBSBIABKL-UHFFFAOYSA-N CAS Database 1450-14-2 (CAS DataBase Reference) NIST Chemical Substance Information Disilane, hexagonal - (1450-14-2) EPA Chemical Substance Information Disilane, hexagonal - (1450-14-2)

  • Hexamethyldisiloxane CAS:107-46-0

    Hexamethyldisiloxane CAS:107-46-0

    Introduction:  Hexamethyldisiloxane (silicone ether, MM sealing agent) is a colorless and transparent liquid that is prone to deliquescence. Insoluble in water, soluble in various organic solvents. Used as silicone oil, silicone rubber, pharmaceuticals, gas chromatography stationary liquids, analytical reagents, hydrophobic agents, etc. Obtained by hydrolysis of trimethylchlorosilane.  The physical properties of hexamethyldisiloxane  colorless and transparent liquids. Easily deliquescent, flammable, and in contact with high heat, open flames, and strong oxidizing agents, there is a risk of combustion. Boiling point 99.5 ℃. Flash point -1.1 ℃. Relative density (d2525) 0.7606. The refractive index is 1.3750. Insoluble in water, soluble in various organic solvents.  Hexamethyldisiloxane is an important primary organic silicon raw material, often used as a capping agent in the production of silicone oil, or as a cleaning agent for silicone rubber, pharmaceuticals, gas c...

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Anhui Techchem Industrial Co.,Ltd. will participate in the Shanghai CPHI China 2026 exhibition.

Anhui Techchem Industrial Co.,Ltd. will participate in the Shanghai CPHI China 2026 exhibition.

Anhui Techchem Industrial Co.,Ltd. will participate in the Shanghai CPHI China 2026 exhibition. The 24th CPHI China 2026 will grandly kick off at the Shanghai New International Expo Center from June 1...

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  • 2-Hydroxy Ethyl Methacrylate CAS: 868-77-9

    2-Hydroxy Ethyl Methacrylate CAS: 868-77-9

    Hydroxyethyl methacrylate (HEMA) is a non-toxic, harmless, and widely used reagent, commonly used for soft lens materials, lens materials, or as a monomer for preparing dense ceramics and glass. Polyhydroxyethyl methacrylate (PHEMA) is a promising biopolymer with significant inertness, biocompatibility, and insolubility. Method 1: Place 100 ml of toluene, 62.1 (1 mol) parts of ethylene glycol, and enzymes (Novozym 435, 0.04 parts, 0.01 parts of sodium carbonate, and 0.01 parts of hydroquinone manufactured by Novo) into a 1-liter glass flask connected to a cooling tube receiver (for measuring moisture) and a reflux side tube, and heat to 40 ° C. 72.1 parts (1mol) of acrylic acid were added in batches within 10 minutes, while stirring step by step. After completing the total addition, the mixture was stirred at the same temperature under reduced pressure of 10mPa. After the reaction, the target acrylate was obtained by filtering and separating the catalyst and additives. The time required for the reaction is approximately 6 hours. The yield and composition of the obtained acrylate were determined by gas chromatography (hereinafter abbreviated as GC). [0044] [Example 2] [0045] Except for changing 72.1 parts (1 mol) of acrylic acid to 86.1 parts (1 mol) of methacrylic acid in Example 1, the target compound was obtained in a similar manner to Example 1. The time required for the reaction is approximately 5 hours. The yield of hydroxyethyl methacrylate (HEMA) was 98.5% by gas chromatography. The synthesis is continuous as shown in Figure 1. Method 2: Add 31.05g ethylene glycol (EG, 0.5mol), 47.35g (0.55mol) methacrylic acid, 40g (inside, 22g water in the catalyst before use, 18g dry weight) strong acid ion exchange resin (Amberlite IR124: gel type, 12% cross-linking degree, no pore), 0.086g HO-TEMPO, 0.086g hydroquinone and 200g toluene into a 500ml glass flask equipped with Dean Stark device, cooling pipe, thermometer and air inlet pipe, Then heat and stir at 100 ℃, while using a pump to add water at a rate of 2g/h. The water formed in the reaction is azeotropic with toluene and removed through the Dean Stark device. After 5 hours, the conversion rate of hydroxyethyl methacrylate was 87.3%. The synthesis is continuous as shown in Figure 1. purpose Hydroxyethyl methacrylate is mainly used for modifying resins and coatings. Copolymerization with other acrylic monomers can produce acrylic resins with active hydroxyl groups in the side chains, which can undergo esterification and crosslinking reactions, synthesize insoluble resins, improve adhesion, and can be used as fiber treatment agents. It reacts with melamine formaldehyde (or urea formaldehyde) resin, epoxy resin, etc. to manufacture two component coatings. Adding it to high-end car paint can maintain the mirror gloss for a long time. It can also be used as an adhesive for synthetic textiles and as a medical polymer monomer

    Tags : 2-Hydroxy Ethyl Methacrylate CAS: 868-77-9 C6H10O3 HEMA

  • 2-hydroxy ethyl methacrylate CAS: 868-77-9

    2-hydroxy ethyl methacrylate CAS: 868-77-9

    Hydroxyethyl methacrylate (HEMA) is a non-toxic, harmless, and widely used reagent, commonly used for soft lens materials, lens materials, or as a monomer for preparing dense ceramics and glass. Polyhydroxyethyl methacrylate (PHEMA) is a promising biopolymer with significant inertness, biocompatibility, and insolubility. Method 1: Place 100 ml of toluene, 62.1 (1 mol) parts of ethylene glycol, and enzymes (Novozym 435, 0.04 parts, 0.01 parts of sodium carbonate, and 0.01 parts of hydroquinone manufactured by Novo) into a 1-liter glass flask connected to a cooling tube receiver (for measuring moisture) and a reflux side tube, and heat to 40 ° C. 72.1 parts (1mol) of acrylic acid were added in batches within 10 minutes, while stirring step by step. After completing the total addition, the mixture was stirred at the same temperature under reduced pressure of 10mPa. After the reaction, the target acrylate was obtained by filtering and separating the catalyst and additives. The time required for the reaction is approximately 6 hours. The yield and composition of the obtained acrylate were determined by gas chromatography (hereinafter abbreviated as GC). [0044] [Example 2] [0045] Except for changing 72.1 parts (1 mol) of acrylic acid to 86.1 parts (1 mol) of methacrylic acid in Example 1, the target compound was obtained in a similar manner to Example 1. The time required for the reaction is approximately 5 hours. The yield of hydroxyethyl methacrylate (HEMA) was 98.5% by gas chromatography. The synthesis is continuous as shown in Figure 1. Method 2: Add 31.05g ethylene glycol (EG, 0.5mol), 47.35g (0.55mol) methacrylic acid, 40g (inside, 22g water in the catalyst before use, 18g dry weight) strong acid ion exchange resin (Amberlite IR124: gel type, 12% cross-linking degree, no pore), 0.086g HO-TEMPO, 0.086g hydroquinone and 200g toluene into a 500ml glass flask equipped with Dean Stark device, cooling pipe, thermometer and air inlet pipe, Then heat and stir at 100 ℃, while using a pump to add water at a rate of 2g/h. The water formed in the reaction is azeotropic with toluene and removed through the Dean Stark device. After 5 hours, the conversion rate of hydroxyethyl methacrylate was 87.3%. The synthesis is continuous as shown in Figure 1. purpose Hydroxyethyl methacrylate is mainly used for modifying resins and coatings. Copolymerization with other acrylic monomers can produce acrylic resins with active hydroxyl groups in the side chains, which can undergo esterification and crosslinking reactions, synthesize insoluble resins, improve adhesion, and can be used as fiber treatment agents. It reacts with melamine formaldehyde (or urea formaldehyde) resin, epoxy resin, etc. to manufacture two component coatings. Adding it to high-end car paint can maintain the mirror gloss for a long time. It can also be used as an adhesive for synthetic textiles and as a medical polymer monomer

    Tags : CAS No. 868-77-9 2-hydroxy ethyl methacrylate

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