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| Product | Description | |
|---|---|---|
| Cellulose acetate | Pharmacopeia & Metrological Institutes Standards; Cation; European Pharmacopoeia (Ph. Eur.); Pharmacopoeial Standards. Uses: For analytical and research use. Group: Reagents. Alternative Names: Cellulose acetate, Cellulose Acetate. CAS No. 9004-35-7. |  |
| Cellulose Acetate | Cellulose Acetate. CAS No. 9004-35-7. Product ID: PE-0205. Molecular formula: [C6H7O2(OH)3-m(OOCCH3)m],m=0~3. Category: Coating Systems Excipients. Product Keywords: Pharmaceutical Excipients; Solid Dosage Form; Coating Systems Excipients; Cellulose Acetate; PE-0205; [C6H7O2(OH)3-m(OOCCH3)m],m=0~3; 9004-35-7; 9004-35-7. Appearance: White Powder. Standard: In-house standard. Grade: Pharmaceutical grade. Purity: 0.99. Solubility: The solubility of cellulose acetate is greatly influenced by the level of acetyl groups present. In general, cellulose acetates are soluble in acetone-water blends of varying ratios, dichloromethane- ethanol blends, dimethyl formamide, and dioxane. Storage: 2-8°C. Boiling Point: 230-300°C. Melting Point: 210 °C. Density: 1.3 g/mL at 25 °C (lit.). |  |
| Cellulose Acetate | Cellulose Acetate. CAS No. 9004-35-7. Product ID: PE-0300. Molecular formula: [C6H7O2(OH)3-m(OOCCH3)m],m=0~3. Category: Sustained & Controlled Release Materials. Product Keywords: Pharmaceutical Excipients; Sustained & Controlled Release Materials; Cellulose Acetate; PE-0300; [C6H7O2(OH)3-m(OOCCH3)m],m=0~3; 9004-35-7; 9004-35-7. Appearance: White Powder. Standard: In-house standard. Grade: Pharmaceutical grade. Purity: 0.99. Solubility: The solubility of cellulose acetate is greatly influenced by the level of acetyl groups present. In general, cellulose acetates are soluble in acetone-water blends of varying ratios, dichloromethane- ethanol blends, dimethyl formamide, and dioxane. Storage: 2-8°C. Boiling Point: 230-300°C. Melting Point: 210 °C. Density: 1.3 g/mL at 25 °C (lit.). | |
| Cellulose Acetate | Cellulose acetate was used in the fabrication of gold microelectrode for electrochemical monochloramine measurement. Cellulose acetate based membranes are used in the separations in aqueous systems and in reverse osmosis process. It has been reported to be used to desalinate seawater.Cellulose acetate was used for biosensor encapsulation. It was used in the preparation of cellulose acetate nanofibre felt structure, cellulose acetate fibers. Uses: Used as a polymer (acetate fibers, yarn, and plastics), waterproofing agent (fabrics), and to make rubber and celluloid substitutes; also used in nonflammable photographic films, varnishes and lacquers, filaments, phonograph records; magnetic tapes, coatings for skins, wire insulation, thermoplastic molds, cell membranes, sewage treatment, and food packaging. Group: Natural polymers and biopolymerspolymers. Alternative Names: Acetylcellulose Cellulose Acetate 9004-35-7 Acetylcellulose Cellulose, acetate Acetate cotton Acetate ester of cellulose Acetose. CAS No. 9004-35-7. Product ID: [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate. Molecular formula: 264.23g/mol. Mole weight: C10H16O8. CC(=O)OCC1C(C(C(C(O1)O)OC(=O)C)O)O. InChI=1S/C10H16O8/c1-4 (11)16-3-6-7 (13)8 (14)9 (10 (15)18-6)17-5 (2)12/h6-10, 13-15H, 3H2, 1-2H3/t6-, 7-, 8+, 9-, 10-/m1/s1. SMEGJBVQLJJKKX-HOTMZDKISA-N. |  |
| Cellulose acetate butyrate | Cellulose acetate butyrate. Group: Natural polymers and biopolymerspolymers. Alternative Names: Cellulose, acetate butanoate. CAS No. 9004-36-8. | |
| Cellulose acetate butyrate, 30-35% | Cellulose acetate butyrate, 30-35%. Group: Polymers. CAS No. 9004-36-8. | |
| Cellulose acetate butyrate, 35-39% | Cellulose acetate butyrate (CAB) is a cellulose mixed fatty acid ester obtained from cellulose, acetic anhydride and butyric anhydride under the action of an acid catalyst. CAB is a thermoplastic resin, and the content of acetyl and butyryl groups in different products varies greatly, which has a great impact on the performance and use of the product. Cellulose acetate butyrate is an additive widely used in the coating industry. Compared with traditional cellulose acetate, it has a wider range of solubility. It not only dissolves in strong polar solvents, but also cellulose acetate butyrate with high butyryl content even Soluble in alcohol solvents. Therefore, CAB is widely used in wood coatings, plastic coatings and other coatings, and has the functions of improving coating fluidity, leveling, outdoor durability, pigment orientation and flexibility. Uses: Used in high-grade coatings, such as uv-curable coatings;photographic chemicals;polymer modification;ink. Group: Polymers. CAS No. 9004-36-8. Molecular formula: Average Mn ~12 kDa. | |
| Cellulose acetate butyrate, 44-50% | Cellulose acetate butyrate (CAB) is a cellulose mixed fatty acid ester obtained from cellulose, acetic anhydride and butyric anhydride under the action of an acid catalyst. CAB is a thermoplastic resin, and the content of acetyl and butyryl groups in different products varies greatly, which has a great impact on the performance and use of the product. Cellulose acetate butyrate is an additive widely used in the coating industry. Compared with traditional cellulose acetate, it has a wider range of solubility. It not only dissolves in strong polar solvents, but also cellulose acetate butyrate with high butyryl content even Soluble in alcohol solvents. Therefore, CAB is widely used in wood coatings, plastic coatings and other coatings, and has the functions of improving coating fluidity, leveling, outdoor durability, pigment orientation and flexibility. Uses: Used in high-grade coatings, such as uv-curable coatings;photographic chemicals;polymer modification;ink. Group: Polymers. CAS No. 9004-36-8. Molecular formula: Average Mn ~12 kDa. | |
| Cellulose acetate butyrate, 50-54% | Cellulose acetate butyrate, 50-54%. Group: Polymers. CAS No. 9004-36-8. | |
| Cellulose acetate hydrogen phthalate | Cas No. 9004-38-0. |  |
| Cellulose acetate - MW 30,000 | Cellulose acetate was used in the fabrication of gold microelectrode for electrochemical monochloramine measurement. Cellulose acetate based membranes are used in the separations in aqueous systems and in reverse osmosis process. It has been reported to be used to desalinate seawater.Cellulose acetate was used for biosensor encapsulation. It was used in the preparation of cellulose acetate nanofibre felt structure, cellulose acetate fibers. Synonyms: Acetic acid, cellulose ester; Acetyl cellulose; Acetylcellulose. CAS No. 9004-35-7. | |
| Cellulose Acetate Ph. Eur | Cellulose Acetate Ph. Eur. CAS No. 9004-35-7. Molecular formula: C2H4O2 (C6H10O5)n. |  |
| Cellulose acetate phthalate | 100g Pack Size. Group: Carbohydrates. Formula: C116H116O64. CAS No. 9004-38-0. Prepack ID 50349243-100g. Molecular Weight 2534.12. See USA prepack pricing. |  |
| Cellulose acetate phthalate | Cellulose is one of the most abundant renewable macromolecular natural resources in the world. Cellulose, hemicellulose and lignin exist in plant cells in a combined or semi-combined manner. Due to the strong interaction between cellulose molecules due to the hydrogen bonding of hydroxyl groups, and the existence of a large number of hydroxyl groups on the cellulose molecular chain, cellulose has strong reactivity. Cellulose acetate phthalate is an enteric coating auxiliary material for preparing capsules and tablets. It is used as an inert substance, but it is also found to have biological activity during use and is used as an embolic material. Uses: Enteric coating excipients for capsules and tablets;preparation of a cellulose/hectorite hybrid composite for purification of phenolic organic wastewater;for the preparation of a pharmaceutical composition comprising a plurality of controlled release coated microparticles. Group: Chemically modified hydrocolloids. CAS No. 9004-38-0. Mole weight: 2534.12 g/mol. Appearance: Powder. Catalog: ACM9004380-1. |  |
| CELLULOSE ACETATE SHEET | CELLULOSE ACETATE SHEET. Group: Polymers. | |
| Cellulose triacetate | Cellulose triacetate is a compound produced from a source of cellulose and acetate (usually acetic anhydride). Triacetates are commonly used in the manufacture of fibers and film bases. It is chemically similar to cellulose acetate. Its distinguishing feature is that in triacetate, at least 92% of the hydroxyl groups are acetylated. During the production of triacetate, cellulose is fully acetylated; in normal cellulose acetate or cellulose diacetate, it is only partially acetylated. The heat resistance of triacetate is significantly higher than that of cellulose acetate. Uses: Plastic film base field: raw material for photographic film base (or film), special film such as x-ray, film base and insulating film separator. aerospace and aerospace materials: materials such as membranes and solid propellant cladding. reverse osmosis membrane: when the acetic acid content is 52.33% ~ 55.95%, cellulose acetate can produce a membrane with excellent performance. Group: Polymers. CAS No. 9012-9-3. Molecular formula: 966.84 g/mol. Mole weight: C6H7O2(OOCH3)3. | |
| Cellulose triacetate | It is widely used in the sustained-release applications and taste masking in pharmaceutical formulatiosn. Synonyms: Cellulose Triacetate Polymer; 2,3,6-Tri-O-acetyl Cellulose; Acetate Flake L 30. CAS No. 9012-9-3. | |
| 01-A-Metals-37mm spiked cassette capsules | 01-A-Metals-37mm spiked cassette capsules. Uses: For analytical and research use. Group: Environmental proficiency testing. Catalog: APS003845. Format: 4 x 37 mm diameter cellulose acetate "cassette capsule" spiked with metal solutions plus 2 x blank capsules. | |
| 1,1,1,2-Tetrachloroethane | 1,?1,?1,?2-?Tetrachloroethane is a chlorinated hydrocarbon and used as a solvent for cellulose, acetate, fat, waxes, greases, rubber, and sulfur. It is a contaminant in groundwater. 1,?1,?1,?2-?Tetrachloroethane can also induce heptotoxicity. Group: Biochemicals. Grades: Highly Purified. CAS No. 630-20-6. Pack Sizes: 1g, 5g. Molecular Formula: C2H2Cl4, Molecular Weight: 167.85. US Biological Life Sciences. |  Worldwide |
| 1,4-Dioxane | 1,4-Dioxane is a heterocyclic organic compound that is commonly used as a solvent in several chemical reactions. It is also used as a stabilizer in chlorinated solvents. Uses: 1,4-dioxane is used as a stabilizer for 1,1,1-trichloroethane and chlorinated solvents. it acts as a solvent for cellulose acetate, ethyl cellulose, benzyl cellulose, resins, oils, waxes, dyes, other organic and inorganic compounds. it acts as a substitute for tetrahydrofuran due to its higher boiling point and lower toxicity. further, it is used as an internal standard for proton nmr spectroscopy in deuterium oxide. it plays an important role in liquid scintillation counting in biological procedures, and as a wetting and dispersing agent in textile processing. it is involved in the preparation of dimethylmagnesium by reacting with methylmagnesium bromide, and in the preparation of histological sections for microscopic examination. Group: Solvents. Alternative Names: dioxane dioxane, technical grade dioxaan-1,4 dioxane-1,4 glycol ethylene ether 1,4-dioxanne glycolethylenether diethylene dioxide dioxan-1,4 diossano-1,4. CAS No. 123-91-1. Molecular formula: C4H8O2. Mole weight: 88.11. IUPACName: 1,4-dioxane. Canonical SMILES: C1COCCO1. Density: 1.033 g/mL. ECNumber: 204-661-8. Catalog: ACM123911-1. | |
| 1-Ethyl-2,3-dimethylimidazolium Acetate | 1-Ethyl-2,3-dimethylimidazolium Acetate is used in the study of cellulose dissolution and solubility. Group: Biochemicals. Grades: Highly Purified. CAS No. 141085-38-3. Pack Sizes: 50mg, 100mg. Molecular Formula: C12H22N2O2, Molecular Weight: 226.17. US Biological Life Sciences. | Worldwide |
| 2-Nitrophenyl octyl ether | 2-Nitrophenyl octyl ether (NPOE) is an organic solvent, which is mainly used as a plasticizer and a charge transferring liquid that can be used in electrochemical devices. Its water solubility is low and has a high molar volume with a relative permittivity of 24.2. Uses: Npoe can be used as a plasticizer in a polymeric inclusion membrane (pim) that enhances the transport of copper(II) in the solution of ammonia. it can be incorporated in a cellulose tri-acetate/carbon nanotube (cta/cnt) based membrane, which is used in the transport and detection of melamine from milk samples. Group: Polymer/macromolecule. Alternative Names: 1-Nitro-2-octyloxybenzene. CAS No. 37682-29-4. Molecular formula: O2NC6H4O(CH2)7CH3. Mole weight: 251.32. Purity: >98.0%(GC). Canonical SMILES: CCCCCCCCOc1ccccc1[N+]([O-])=O. Density: 1.04 g/mL at 25 °C (lit.). ECNumber: 253-623-7. Catalog: ACM37682294-1. | |
| Acetic Anhydride-d6 | Acetic Anhydride-d6 is the labeled analog of acetic anhydride, a reagent used generally in acetylation reactions in organic chemistry, primarily cellulose acetate and film material. Group: Biochemicals. Alternative Names: Hexadeuterioacetic Anhydride; Perdeuterioacetic Anhydride; 1,1'-Anhydride Acetic-2,2,2-d3 Acid. Grades: Highly Purified. CAS No. 16649-49-3. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Cellacefate | Cellacefate. CAS No. 9004-38-0. Product ID: PE-0208. Molecular formula: C116H116O64. Mole weight: 2534.12. Category: Coating Systems Excipients. Product Keywords: Pharmaceutical Excipients; Solid Dosage Form; Coating Systems Excipients; Cellacefate; PE-0208; C116H116O64; 9004-38-0; 9004-38-0. Appearance: Neat. Standard: USP. Grade: Pharmaceutical primary standard. Synonym(s): Cellulose acetate phthalate. Solubility: Practically insoluble in water, freely soluble in acetone, soluble in diethylene glycol, practically insoluble in ethanol (96 per cent) and in methylene chloride. It dissolves in dilute solutions of alkali hydroxides. Storage: Cellulose acetate phthalate is stable if stored in a well-closed container in a cool, dry place. | |
| Cellobiohydrolase I from Hypocrea jecorina, Recombinant | Cellulose 1,4-beta-cellobiosidase (non-reducing end) is an enzyme with system name 4-beta-D-glucan cellobiohydrolase (non-reducing end). This enzyme catalyses the following chemical reaction:Hydrolysis of (1->4)-beta-D-glucosidic linkages in cellulose and cellotetraose, releasing [cellobiose] from the non-reducing ends of the chains. Cellubiohydrolase i is an enzyme present in many fungi, but particularly wood rot fungi. it is a monomer of 53 kda with a catalytic domain and a cellulose binding domain. the reaction adds water to the glucose bonds in cellulose (non-reducing ends of the chain), yielding cellobiose. Applications: Cellobiohydrolase i can be used in com...ellobiohydrolase; 1,4-beta-D-glucan cellobiohydrolase. Enzyme Commission Number: EC 3.2.1.91. CAS No. 253-465-9. Cellulose 1,4-beta-cellobiosidase. Activity: 0.13 U/mg. Form: Enzyme is provided in a sodium acetate and ammonium sulfate solution, containing 0.02% sodium azide. Source: Corn. Species: Hypocrea jecorina. Cellobiohydrolase I; Cellobiosidase; EC 3.2.1.91; Cel7A; Cellulase; exo-cellobiohydrolase; beta-1,4-glucan cellobiohydrolase; beta-1,4-glucan cellobiosylhydrolase; 1,4-beta-glucan cellobiosidase; exoglucanase; avicelase; CBH 1; C1 cellulase; cellobiohydrolase; exo-beta-1,4-glucan cellobiohydrolase; 1,4-beta-D-glucan cellobiohydrolase. Cat No: NATE-0112. |  |
| Cellulose, adhesive-free, powder, for TLC | Cellulose, adhesive-free, powder, for TLC. Group: Polymers. CAS No. 9004-35-7. Product ID: [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate. Molecular formula: 264.23g/mol. Mole weight: C10H16O8. CC(=O)OCC1C(C(C(C(O1)O)OC(=O)C)O)O. InChI=1S/C10H16O8/c1-4 (11)16-3-6-7 (13)8 (14)9 (10 (15)18-6)17-5 (2)12/h6-10, 13-15H, 3H2, 1-2H3/t6-, 7-, 8+, 9-, 10-/m1/s1. SMEGJBVQLJJKKX-HOTMZDKISA-N. | |
| Cellulose propionate | Cellulose propionate. Group: Natural polymers and biopolymers. Alternative Names: Cellulose,acetatepropanoate; CELLULOSE PROPIONATE; CELLULOSE ACETATE PROPIONATE; CELLULOSE ACETATE PROPIONATE, 42.5 WT. %PROPIONYL CONTENT, AVE. MN CA. 15,000; CELLULOSE ACETATE PROPIONATE, 46 WT. % P ROPIONYL CONTENT, AVE. MN CA. 75,000; CELLULOSE ACETATE PRO. CAS No. 9004-39-1. Product ID: 2-(hydroxymethyl)-6-[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol; [4,5,6-triacetyloxy-3-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate; [4,5,6-tri(propanoyloxy)-3-[3,4,5-tri(propanoyloxy)-6-(propanoyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl propanoate. Molecular formula: 1811.7g/mol. Mole weight: C76H114O49. CCC (=O)OCC1C (C (C (C (O1)OC (=O)CC)OC (=O)CC)OC (=O)CC)OC2C (C (C (C (O2)COC (=O)CC)OC (=O)CC)OC (=O)CC)OC (=O)CC. CC (=O)OCC1C (C (C (C (O1)OC (=O)C)OC (=O)C)OC (=O)C)OC2C (C (C (C (O2)COC (=O)C)OC (=O)C)OC (=O)C)OC (=O)C. C (C1C (C (C (C (O1)OC2C (OC (C (C2O)O)O)CO)O)O)O)O. InChI=1S/C36H54O19. C28H38O19. C12H22O11/c1-9-21 (37)45-17-19-29 (49-23 (39)11-3)31 (50-24 (40)12-4)34 (53-27 (43)15-7)36 (48-19)55-30-20 (18-46-22 (38)10-2)47-35 (54-28 (44)16-8)33 (52-26 (42)14-6)32 (30)51-25 (41)13-5; 1-11 (29)37-9-19-21 (39-13 (3)31)23 (40-14 (4)32)26 (43-17 (7)35)28 (46-19)47-22-20 (10-38-12 (2)30)45-27 (44-18 (8)36)25 (42-16 (6)34)24 (22)41-15 (5)33; 13-1-3-5 (15)6 (16)9 (19)12 (22-3)23-10-4 (2-14)21 | |
| Di-(2-Ethylhexyl) (2-(2-Hydroxyethyl)-hexyl) Phosphate | Di-(2-Ethylhexyl) (2-(2-Hydroxyethyl)-hexyl) Phosphate is derived from γ-Butyrolactone (B760995), which is a solvent for polyacrylonitrile, cellulose acetate, methyl methacrylate polymers, polystyrene. Constituent of paint removers, textile aids, drilling oils. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C24H51O5P, Molecular Weight: 450.63. US Biological Life Sciences. | Worldwide |
| Dimethyl Phthalate | Dimethyl phthalate is a organic compound with molecular formula (C2H3O2)2C6H4. The methyl ester of phthalic acid, it is a Colorless liquid that is soluble in organic solvents.Dimethyl phthalate is used as an insect repellent for mosquitoes and flies. It is also an ectoparasiticide and has many other uses, including in solid rocket propellants, and plastics. Its LD50 is 8 200 mg/kg (rats, oral). Uses: Dmp can be used to plasticize cellulose acetate which can be further used in the production of laminated safety glass for flight helmets and goggles. it can be used as a plasticizer that forms complexes with polyvinyl alcohol (pva) and lithium salts for the development of solid polymer electrolyte (spe) for solar cell (sc) s. it may also be used as a mixture of polymeric solvents which can be used in the preparation of polyvinylidene fluoride (pvdf). Group: Heterocyclic organic compound. Alternative Names: DMP. CAS No. 131-11-3. Molecular formula: C10H10O4. Mole weight: 194.2. Appearance: Oil. Purity: 0.98. IUPACName: dimethyl benzene-1,2-dicarboxylate. Canonical SMILES: COC(=O)C1=CC=CC=C1C(=O)OC. Density: 1.192. ECNumber: 205-011-6. Catalog: ACM131113-3. | |
| Dimethyl Phthalate | Dimethyl phthalate is a organic compound with molecular formula (C2H3O2)2C6H4. The methyl ester of phthalic acid, it is a Colorless liquid that is soluble in organic solvents.Dimethyl phthalate is used as an insect repellent for mosquitoes and flies. It is also an ectoparasiticide and has many other uses, including in solid rocket propellants, and plastics. Its LD50 is 8 200 mg/kg (rats, oral). Uses: Dmp can be used to plasticize cellulose acetate which can be further used in the production of laminated safety glass for flight helmets and goggles. it can be used as a plasticizer that forms complexes with polyvinyl alcohol (pva) and lithium salts for the development of solid polymer electrolyte (spe) for solar cell (sc) s. it may also be used as a mixture of polymeric solvents which can be used in the preparation of polyvinylidene fluoride (pvdf). Group: Plastic additivespolymersplasticizers. Alternative Names: DMP. CAS No. 131-11-3. Pack Sizes: Packaging 1, 4 L in poly bottle. Product ID: dimethyl benzene-1,2-dicarboxylate. Molecular formula: 194.2. Mole weight: C10H10O4. COC(=O)C1=CC=CC=C1C(=O)OC. InChI=1S/C10H10O4/c1-13-9 (11)7-5-3-4-6-8 (7)10 (12)14-2/h3-6H, 1-2H3. NIQCNGHVCWTJSM-UHFFFAOYSA-N. 98%. | |
| Ethyl lactate,C5H10O3,97-64-3 | Ethyl Lactate is a solvent manufactured from l(+) lactic acid which is miscible in water and most organic solvents and is cleared for use as a flavoring agent. it is a naturally occurring constituent of california and spanish sherries. it is a clear, colorless, nontoxic liquid of low volatility, having a ph of 7-7.5. it is used as a food and beverage flavoring agent.formulationsand recently as a co-solvent in emulsions and microemulsion technologies. It has also been used as a solvent for nitrocellulose, cellulose acetate, cellulose ethers, polyvinyl and other resins. It has been applied topically in the treatment of acne vulgaris,where it accumulates in the sebaceous glands and is hydrolyzed to ethanol and lactic acid, lowering the skin pH and exerting a bactericidal effect. Group: Platinum catalysts. Alternative Names: ethyl-lactate; Ethyl racemic-lactate; I14-2597; Ethyl 2-hydroxypropanoate; Mono-Ethyl mono-lactate; Tox21_200889; SY030456; Lactic acid, ethyl ester; L0003; Propanoicacid, 2-hydroxy-, ethyl ester, (2R)-. CAS No. 97-64-3. Molecular formula: C5H10O3. Mole weight: 118.132g/mol. IUPACName: ethyl 2-hydroxypropanoate. Canonical SMILES: CCOC(=O)C(C)O. Density: 1.03 at 68 ° F (USCG, 1999);1.0328 g.cu cm at 20 deg C;1.03. ECNumber: 202-598-0. Catalog: ACM97643. | |
| GAA. (Glacial Acetic Acid 99%) | GAA. (Glacial Acetic Acid 99%). Uses: Chemical industry: raw material in the production of various chemical compounds, such as ethyl acetate, vinyl acetate, cellulose acetate and other esters. -food and beverage industry: used as a food additive in the food and beverage industry. -textile industry: used in the textile dyeing and finishing process. helps fix dyes in textile fibers and improve color fastness. - cleaning and disinfection industry: cleaning and disinfection products due to their antimicrobial properties. it can be used to remove stains, descale surfaces and disinfect areas. ?. Purity: Industrial. CAS No. 64-19-7. Pack Sizes: BULK. Product ID: UN2789. |  |
| γ-Butyrolactone-d4 | γ-Butyrolactone-d4 is an isotope labelled solvent for polyacrylonitrile, cellulose acetate, methyl methacrylate polymers, polystyrene. Constituent of paint removers, textile aids, drilling oils. Group: Biochemicals. Grades: Highly Purified. CAS No. 1224441-94-4. Pack Sizes: 25mg, 100mg. Molecular Formula: C4H2D4O2. US Biological Life Sciences. | Worldwide |
| γ-Butyrolactone-d6 | γ-Butyrolactone-d6 is an isotope labelled solvent for polyacrylonitrile, cellulose acetate, methyl methacrylate polymers, polystyrene. Constituent of paint removers, textile aids, drilling oils. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 250mg. Molecular Formula: C4D6O2. US Biological Life Sciences. | Worldwide |
| Hypromellose Acetate Succinate | Hypromellose acetate succinate is a white to off-white powder or granules. It has a faint acetic acid-like odor and a barely detectable taste. Hypromellose acetate succinate is available in several grades, according to the pH at which the polymer dissolves (low, L; medium, M; and high, H) and its predominant particle size (cohesive fine powder, F; or free-flowing granules, G). Synonyms: Aqoat; Aqoat AS-HF/HG; Aqoat AS-LF/LG; Aqoat AS-MF/MG; cellulose, 2-hydroxypropyl methyl ether, acetate succinate; HPMCAS. CAS No. 71138-97-1. Product ID: PE-0594. Category: Controlled-release Agents; Coating Agents; Film-forming Agents; Sustained-release Agents. Product Keywords: Excipients for Liquid Dosage Form; Solubilizer Excipients; PE-0594; Hypromellose Acetate Succinate; Controlled-release Agents; Coating Agents; Film-forming Agents; Sustained-release Agents; ; 71138-97-1. UNII: NA. Chemical Name: Cellulose, 2-hydroxypropylmethyl ether, acetate hydrogen butanedioate. Grade: Pharmceutical Excipients. Administration route: Oral. Dosage Form: Capsules, and delayed-action preparations. Stability and Storage Conditions: Hypromellose acetate succinate should be stored in a well-closed container, in a cool, dry place. In such storage conditions, hypromellose acetate succinate is a stable material. Hypromellose acetate succinate is hygroscopic. It is hydrolyzed to acetic acid and succinic acid, and the hypromellose po | |
| Meldola Blue | A biosensor for the measurement of lactate in serum has been developed, which is based on a screen-printed carbon electrode, modified with Meldola's Blue-Reinecke Salt (MBRS-SPCE), coated with the enzyme lactate dehydrogenase NAD+ dependent (from Porcine heart), and NAD+. A cellulose acetate layer was deposited on the top of the device to act as a permselective membrane. Group: Biochemicals. Alternative Names: 9- (Dimethylamino) benzo[a]phenoxazin-7-ium Chloride Zinc Chloride; Meldola's Blue; Zinc Chloride 9- (Dimethylamino) benzo[a]phenoxazin-7-ium Chloride; Basic Leather Blue D; Meldola Blue. CAS No. 7057-57-0. Pack Sizes: 2.5mg. Molecular Formula: C??H??ClN?O xZnCl?. US Biological Life Sciences. | Worldwide |
| N-Ethyl-p-toluenesulfonamide | N-Ethyl-4-toluene sulfonamide is a resin carrier in dental materials used for isolating cavities below restorations; plasticizer in polyvinyl alcohollacquers, polyamides, cellulose acetate, etc. Group: Heterocyclic organic compound. CAS No. 80-39-7. Molecular formula: C9H13NO2S. Mole weight: 199.27. Appearance: Off-white crystalline solid. Purity: MP 63-64.5deg. Density: 1.153 g/cm³. Catalog: ACM80397. | |
| Phenoxyethanol (CAS 122-99-6) | Phenoxyethanol is a colorless liquid with a slightly floral odor. It is a commonly used preservative in various cosmetic products such as skincare, haircare, and makeup products. It has broad-spectrum antimicrobial properties that help to prevent the growth of bacteria, yeast, and mold in these products. Additionally, it can also be used as a fragrance enhancer and solvent in cosmetics. Uses: 1. phenoxyethanol is used as a preservative in various cosmetic products, such as creams, lotions, and shampoos. 2. it is also used as a stabilizer in perfumes and soaps. 3. phenoxyethanol has been used as a bactericide in vaccines and in medicine as a local anesthetic. 4. it is also used in industrial applications as a solvent for cellulose acetate, dyes, and inks. 5. phenoxyethanol is known for its antimicrobial properties and acts by inhibiting the growth of bacteria and fungi in various products. Group: Hair actives. CAS No. 122-99-6. Appearance: clear, oily liquid with a faint rose-like odor. Catalog: CI-HC-0211. | |
| Tributyl Phosphate (TBP) | The products are mainly used as plasticizers for cellulose acetate, nitrocellulose, chlorinated rubber and PVC, solvents for paints, inks and adhesives, defoamers and antistatic agents, and organic synthetic intermediates; It is also used as building material additive, lubricating oil, pressure resistance and anti-wear agent; It is used as flame retardant of aircraft hydraulic oil and solvent for extraction and purification of rare earth elements, defoamer of oil casing well cement, solvent for processing nuclear fuel, carrier of fluorescent dyes and extractant for purification of wet process phosphoric acid. Group: Phosphate ester flame retardant. Alternative Names: Tributyl phosphate(TBP). CAS No. 126-73-8. Appearance: colorless transparent liquid. Purity: ≥ 99%. Catalog: ACM126738. | |
| 2,3,6,2,3,4,6-Hepta-O-acetyl-a-D-cellobiosyl fluoride | 2,3,6,2,3,4,6-Hepta-O-acetyl-a-D-cellobiosyl fluoride is a derivative originating from cellulose. This compound assumes a pivotal role in facilitating theresearch and development of groundbreaking pharmaceuticals that target ailments associated with carbohydrate metabolism and glycogen storage disorders. Synonyms: Peracetylated cellobiosyl fluoride. CAS No. 14227-64-6. Molecular formula: C26H35FO17. Mole weight: 638.54. | |
| Bis(2,4-pentanedionato)titanium(IV) Oxide | Bis(2,4-pentanedionato)titanium(IV) Oxide. Uses: Cross-linking agent for cellulosic lacquers. Group: Salt. Alternative Names: Titanium(IV)oxide acetylacetonate; Titanyl acetylacetonate; ZMTWFOKZRDNMEJ-SUKNRPLKSA-L; Bis(2,4-pentanedionato)titanium oxide; AKOS025311138; 14024-64-7; MFCD00013505; Titanium, oxobis(2,4-pentanedionato-.kappa.O. kappa.O')-; Titanium(IV) oxide bis(2,4-pentanedionate). CAS No. 14024-64-7. Product ID: (Z)-4-hydroxypent-3-en-2-one; oxotitanium. Molecular formula: 264.1g/mol. Mole weight: C10H16O5Ti. CC(=CC(=O)C)O.CC(=CC(=O)C)O.O=[Ti]. InChI=1S/2C5H8O2. O. Ti/c2*1-4(6)3-5(2)7; ; /h2*3, 6H, 1-2H3; ; /b2*4-3-; ;. ADVORQMAWLEPOI-SUKNRPLKSA-N. | |
| Bis(2,4-pentanedionato)titanium(IV) Oxide | Cross-linking agent for cellulosic lacquers. Group: Micro/nanoelectronics. Alternative Names: Titanium(IV)oxide acetylacetonate; Titanyl acetylacetonate; ZMTWFOKZRDNMEJ-SUKNRPLKSA-L; Bis(2,4-pentanedionato)titanium oxide; AKOS025311138; 14024-64-7; MFCD00013505; Titanium, oxobis(2,4-pentanedionato-.kappa.O. kappa.O')-; Titanium(IV) oxide bis(2,4-pentanedionate). CAS No. 14024-64-7. Molecular formula: C10H16O5Ti. Mole weight: 264.1g/mol. IUPACName: (Z)-4-hydroxypent-3-en-2-one;oxotitanium. Canonical SMILES: CC(=CC(=O)C)O.CC(=CC(=O)C)O.O=[Ti]. ECNumber: 237-861-9. Catalog: ACM14024647. | |
| C-19 steroid 1α-hydroxylase | The enzyme, characterized from the bacterium Sorangium cellulosum, is a class I cytochrome P-450, and uses ferredoxin as its electron donor. It was shown to act on several C-19 steroid substrates, including testosterone, androstenedione, testosterone-acetate and 11-oxoandrostenedione. Group: Enzymes. Synonyms: CYP260A1. Enzyme Commission Number: EC 1.14.15.19. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0944; C-19 steroid 1α-hydroxylase; EC 1.14.15.19; CYP260A1. Cat No: EXWM-0944. | |
| Carmellose | Pharmacopeia & Metrological Institutes Standards; European Pharmacopoeia (Ph. Eur.); Pharmacopoeial Standards. Uses: For analytical and research use. Group: Reagents. Alternative Names: Almelose, Colloresine, Finnfix GDA, Apergel, Mavibond CP-O 8000, Cellulose carboxymethylate, Carbose, Cellogen BSH 10, HV-CMC, CM-Cellulose, Carboxylmethyl cellulose, Glycolic acid cellulose ether, Glycocel TA, Cellulose, (carboxymethyl)-, CMC 4LF,Acetic acid, hydroxy-, cellulose ether, Celluloseglycolic acid, Cellulose Gum 7H, Carboxymethyl cellulose ether, Carboxymethyl cellulose, KMTs, Carboxymethylated cellulose pulp, Apeyel, Cellulose, ether with glycolic acid, Celish KY 100G carboxymethyl ether, Duodcel, Finnfix 2, Finnfix V, CMC, Carmellose. CAS No. 9000-11-7. Pack Sizes: 500MG. | |
| Cellulase 5C & Acetyl xylan esterase 2A from Clostridium thermocellum, Recombinant | Cellulase is any of several enzymes produced chiefly by fungi, bacteria, and protozoans that catalyze cellulolysis, the decomposition of cellulose and of some related polysaccharides; specifically, the hydrolysis of the 1,4-beta-D-glycosidic linkages in cellulose, hemicellulose, lichenin, and cereal beta-D-glucans. Cellulases break down the cellulose molecule into monosaccharides ("simple sugars") such as beta-glucose, or shorter polysaccharides and oligosaccharides. The name is also used for any naturally occurring mixture or complex of various such enzymes, that act serially or synergistically to decompose cellulosic material. Group: Enzymes. Synony...is enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium thermocellum. Cellulase, thermostable; 1,4-(1,3:1,4)-β-D-Glucan 4-glucano-hydrolase; EC 3.2.1.4; Cellulase; endo-1,4-β-D-glucanase; β-1,4-glucanase; β-1,4-endoglucan hydrolase; celluase A; cellulosin AP; endoglucanase D; alkali cellulase; cellulase A 3; celludextrinase; 9.5 cellulase; avicelase; pancellase SS; Cellulase 5C; Acetylxylan esterase; EC 3.1.1.72; Acetyl xylan esterase 2A. Cat No: NATE-1374. | |
| Cellulose microcrystalline | Cellulose microcrystalline. CAS No. 9004-34-6. Product ID: CDC10-0017. Molecular formula: C6H10O5. Category: Cosmetic Chemical Abrasives. Product Keywords: Cosmetic Ingredients; Cosmetic Chemical Abrasives; Cellulose microcrystalline; CDC10-0017; 9004-34-6; C6H10O5; 232-674-9; 9004-34-6. Purity: 0.99. Color: White or almost white. EC Number: 232-674-9. Physical State: Powder. Solubility: Practically insoluble in water, in acetone, in anhydrous ethanol, in toluene, in dilute acids and in a 50 g/L solution of sodium hydroxide. Storage: Store at room temperature. Boiling Point: 237.6±35.0 °C at 760 mmHg. Melting Point: 260-270ºC. Density: 0.9±0.1 g/cm3. | |
| Chitin | The monomers are identified as N-Acetyl-Amnioglucose. Chitin is a polysaccharide containing nitrogen in which monomers occur with the glycosidically linked components beta 1,4. It is the same coupling as glucose with cellulose, however in chitin the hydroxyl group of the monomer is replaced with an acetyl amine group. The resulting, stronger hydrogen bond between the bordering polymers makes chitin harder and more stabile than cellulose. Group: Biomaterials. Alternative Names: (1,4)-N-acetyl-D-glucos-2-amine. CAS No. 1398-61-4. Molecular formula: (C8H13NO5)n. Mole weight: 161.16. Appearance: White to beige solid. Purity: 0.96. IUPACName: N-[(2R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide. Canonical SMILES: CC(=O)NC1[C@@H](OC(C(C1O)O)CO)O. Density: 1.37g/ml. Catalog: ACM1398614. | |
| Chitin | The monomers are identified as N-Acetyl-Amnioglucose. Chitin is a polysaccharide containing nitrogen in which monomers occur with the glycosidically linked components beta 1,4. It is the same coupling as glucose with cellulose, however in chitin the hydroxyl group of the monomer is replaced with an acetyl amine group. The resulting, stronger hydrogen bond between the bordering polymers makes chitin harder and more stabile than cellulose. Group: Polymers. Alternative Names: (1,4)-N-acetyl-D-glucos-2-amine. CAS No. 1398-61-4. Pack Sizes: 1 ton. Product ID: N-[(2R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide. Molecular formula: 161.16. Mole weight: (C8H13NO5)n. CC(=O)NC1[C@@H](OC(C(C1O)O)CO)O. OVRNDRQMDRJTHS-WTZNIHQSSA-N. InChI=1S/C8H15NO6/c1-3 (11)9-5-7 (13)6 (12)4 (2-10)15-8 (5)14/h4-8, 10, 12-14H, 2H2, 1H3, (H, 9, 11)/t4?, 5?, 6?, 7?, 8-/m1/s1. 96%. | |
| Chitinase 18A from Bacillus cereus, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.14. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 38.3 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus cereus. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 18A. Cat No: NATE-1377. | |
| Chitinase 18A from Bacillus licheniformis, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.14. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 49.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus licheniformis. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 18A. Cat No: NATE-1378. | |
| Chitinase 18A from Clostridium thermocellum, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.14. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 43.9 kDa. Activity: 25 U/mg. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium thermocellum. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 18A. Cat No: NATE-1379. | |
| Chitosanase 46A from Bacillus subtilis, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 29.5 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 46A. Cat No: NATE-1376. | |
| Chitosanase 8B from Bacillus cereus, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 47.8 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus cereus. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 8B. Cat No: NATE-1375. | |
| Levulinic Acid | Levulinic Acid is derived from the degredation of cellulose and is a potential precursor to biofuels. Levulinic acid is also a photosensitizer for photodynamic therapy. Group: Biochemicals. Alternative Names: 3-Acetylpropionic Acid; 3-Oxobutanecarboxylic Acid; 4-Ketovaleric Acid; 4-Oxopentanoic Acid; 4-Oxovaleric Acid; Laevulinic Acid; Levulic Acid; NSC 3716; β-Acetylpropionic Acid; γ-Ketovaleric Acid. Grades: Highly Purified. CAS No. 123-76-2. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| Native Streptomyces griseus Chitosanase | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Applications: Chitosanase from streptomyces griseus has been used in a study to assess the effect of chitin sources on production of chitinase and chitosanase. chitosanase from streptomyces griseus has also been used in a study to investigate the effective production of chitinase an...cete aphanomyces euteiches, a major parasite of legume plants. it has also been used for the enzymatic hydrolysis of the fully de-n-acetylated chitosan to get chitosan oligomer mixtures during the preparation of biocompatible chitosan-alginate gel. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.132. CAS No. 51570-20-8. Chitosanase. Activity: >50 units/mg protein (Bradford). Storage: -20°C. Form: Lyophilized powder containing potassium phosphate buffer salts. Source: Streptomyces griseus. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Cat No: NATE-0125. | |
| Xanthan gum | Xanthan gum is a kind of microbial polysaccharide produced by Xanomonas campestris. The structure of xanthan is based on a cellulosic backbone of β-(1-4)-linked glucose units which have a trisaccharide side chain of mannose-glucuronic acid-mannose linked to every second glucose unit in the main chain. Some terminal mannose units are pyruvylated and some of the inner mannose units are acetylated. Due to its unique rheological and gelatinous properties, it is widely used in the food and petroleum industry as a food additive, thickener and stabilizer. Uses: Shampoo shower gel body care face care. Synonyms: Corn sugar gum; E415; Grindsted; Keldent; Keltrol; polysaccharide B-1459; Rhodicare S; Rhodigel; Vanzan NF; xanthani gummi; Xantural. CAS No. 11138-66-2. Molecular formula: (C35H49O29)n. | |
| Xanthan gum | Xanthan gum is a microbial polysaccharide produced by Xanthomonas campestris. The structure of xanthan gum is based on a cellulose backbone of β-(1-4)-linked glucose units with a trisaccharide side of mannose-glucuronic acid-mannose attached to every other glucose unit in the backbone chain. Some terminal mannose units are pyruvated and some internal mannose units are acetylated. Due to its unique rheology and gelling properties, it is widely used as a food additive, thickener and stabilizer in the food and petroleum industries. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 11138-66-2. Pack Sizes: 500 g. Product ID: HY-A0103. |  |
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