Product details： Fatty Alcohol Ethoxylate 10mol (Laureth-10) CAS NO. 68439-50-9 Payment:T/T Min order:1000kg Lead time:7-15 days

Product details： Fatty Alcohol Ethoxylate 12 mol CAS NO. 68439-50-9 Payment:T/T Min order:1000l Lead time:7-15 days

Product details： Sodium Alpha-olefin Sulfonate CAS NO. 68439-57-6 Payment:T/T Min order:1000kg Lead time:7-15 days

Product details： APG 0810 CAS NO. 68515-73- 1 Payment:T/T Min order:1000kg Lead time:7-15 days

Product details： APG1214 CAS NO. 110615-47-9 Payment:T/T Min order:1000kg Lead time:7-15 days

Product details： 1-Octadecanol  CAS NO. 112-92-5 Payment:T/T Min order:1000kg Lead time:7-15 days

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

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

Name:  Heptamethyldisilazane CAS No.:  920-68-3 Molecular formula: C7H21NSi2 Molecular weight: 175.42 UN Number: 2924 Product standard: HG/T 5797-2021 Appearance: Colorless transparent liquid

Name:  Chlorodimethylphenylsilane CAS No.:  768-33-2 Appearance: Colorless or light yellow liquid Molecular weight: 170.71 Relative density: 1.032 Purity: ≥98.0% Flash point: 61℃ Boiling point: 198℃ Melting point: ＜0℃ Refractive index nD20:1.506-1.510

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. Widely used in the treatment of organic silicone and white carbon black.

Name: Dichroromethylvinylsilane CAS number: 124-70-9 Molecular formula: C3H6Cl2Si Molecular weight: 141.07 EINECS number: 204-710-3 Mol file: 124-70-9.mol