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| Product | Description | |
|---|---|---|
| 2-(2H-Benzotriazol-2-yl)-4,6-bis(1-methyl-1-phenylethyl)phenol | 2-(2H-Benzotriazol-2-yl)-4,6-bis(1-methyl-1-phenylethyl)phenol. Uses: Low volatile benzotriazole uv light absorber and stabilizer. imparts outstanding light stability for polymers processed at high temperatures such as polycarbonate, polyesters, polyacetal, polyamides, polyphenylene sulfide, polyphenylene oxide, aromatic copolymers, thermoplastic polyurethane and polyurethane fibers also highly effective for polyvinylchloride, styrene homo- and copolymers. Group: Plastic additives. Alternative Names: 2-(2-Hydroxy-3,5-dicumyl)benzotriazole, 2-[2-Hydroxy-3, 5-bis(α, α-dimethylbenzyl)phenyl]-2H -benzotriazole, 2-(2-Hydroxy-3,5-di-α-cumylphenyl)-2H -benzotriazole, 2-(3', 5'-Bis(α, α-dimethylbenzyl)-2'-hydroxyphenyl)benzotriazole, 2-(Benzotriazol-2-yl)-4,6-bis(2-phenylpropan-2-yl)phenol, 2-(2H -Benzotriazol-2-yl)-4,6-bis(1-methyl-1-phenylethyl)phenol, 2-(2H -Benzotriazol-2-yl)-4,6-bis(1-methyl-l-phenylethyl)phenol. CAS No. 70321-86-7. Pack Sizes: Packaging 100 g in glass bottle. Product ID: 2-(benzotriazol-2-yl)-4,6-bis(2-phenylpropan-2-yl)phenol. Molecular formula: 447.57. Mole weight: C30H29N3O. CC (C) (c1ccccc1)c2cc (c (O)c (c2)C (C) (C)c3ccccc3)-n4nc5ccccc5n4. 1S/C30H29N3O/c1-29 (2, 21-13-7-5-8-14-21)23-19-24 (30 (3, 4)22-15-9-6-10-16-22)28 (34)27 (20-23)33-31-25-17-11-12-18-26 (25)32-33/h5-20, 34H, 1-4H3. OLFNXLXEGXRUOI-UHFFFAOYSA-N. 99%. |  |
| 2-(2H-Benzotriazol-2-yl)-4,6-bis(1-methyl-1-phenylethyl)phenol | Low volatile benzotriazole UV light absorber and stabilizer. Imparts outstanding light stability for polymers processed at high temperatures such as polycarbonate, polyesters, polyacetal, polyamides, polyphenylene sulfide, polyphenylene oxide, aromatic copolymers, thermoplastic polyurethane and polyurethane fibers also highly effective for polyvinylchloride, styrene homo- and copolymers. Group: Polymer/macromolecule. Alternative Names: 2-(2-Hydroxy-3,5-dicumyl)benzotriazole, 2-[2-Hydroxy-3, 5-bis(α, α-dimethylbenzyl)phenyl]-2H -benzotriazole, 2-(2-Hydroxy-3,5-di-α-cumylphenyl)-2H -benzotriazole, 2-(3', 5'-Bis(α, α-dimethylbenzyl)-2'-hydroxyphenyl)benzotriazole, 2-(Benzotriazol-2-yl)-4,6-bis(2-phenylpropan-2-yl)phenol, 2-(2H -Benzotriazol-2-yl)-4,6-bis(1-methyl-1-phenylethyl)phenol, 2-(2H -Benzotriazol-2-yl)-4,6-bis(1-methyl-l-phenylethyl)phenol. CAS No. 70321-86-7. Molecular formula: C30H29N3O. Mole weight: 447.57. Purity: 0.99. IUPACName: 2-(benzotriazol-2-yl)-4,6-bis(2-phenylpropan-2-yl)phenol. Canonical SMILES: CC (C) (c1ccccc1)c2cc (c (O)c (c2)C (C) (C)c3ccccc3)-n4nc5ccccc5n4. Density: 1.12 g/cm³. ECNumber: 274-570-6. Catalog: ACM70321867-2. |  |
| 2-[4,6-Bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)phenol | 2-[4,6-Bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)phenol is used as a stabilizer for olefin polymers intended for use in contact with food. 2-[4,6-Bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)phenol is also used as UV light absorber/stabilizer in other polymers. Group: Biochemicals. Alternative Names: 2-(4,6-Di-2,4-xylyl-s-triazin-2-yl)-5-(octyloxy)phenol; 2,4-Bis(2,4-dimethylphenyl)-6-(2-hydroxy-4-n-octyloxyphenyl)-1,3,5-triazine; 2,4-Bis(2,4-dimethylphenyl)-6-(2-hydroxy-4-octyloxyphenyl)-1,3,5-triazine; 2,4-Bis(2,4-dimethylphenyl)-6-(2-hydroxy-4-octyloxyphenyl)-s-triazine; 2,6-Bis(2,4-dimethylphenyl)-4-(2-hydroxy-4-octyloxyphenyl)-s-triazine; 2-(4,6-Bis(2,4-dimethylphenyl)-1,3,5-triazine-2-yl)-5-octyloxyphenol; Cyagard UV 1164; Cyasorb 1164; Cyasorb UV 1164; Cytec UV 1164; Tinuvin 1545; UV 1164. Grades: Highly Purified. CAS No. 2725-22-6. Pack Sizes: 1g. US Biological Life Sciences. |  Worldwide |
| 2-(4,6-Diphenyl-1,3,5-triazine-2-yl)-5-[(hexyl)oxy]phenol | 2-(4,6-Diphenyl-1,3,5-triazine-2-yl)-5-[(hexyl)oxy]phenol is used as a light stabilizer/UV absorber for polyethylene phthalate polymers intended for use in contact with food. Group: Biochemicals. Alternative Names: 2,4-Diphenyl-6-(2-hydroxy-4-hexyloxyphenyl)-s-triazine; 2,4-Diphenyl-6-[2-hydroxy-4-(hexyloxy)phenyl]-1,3,5-triazine; 2-(2-Hydroxy-4-hexyloxyphenyl)-4,6-diphenyl-1,3,5-triazine; 2-(4,6-Diphenyl-1,3,5-triazin-2-yl)-5-hexyloxyphenol; 2-(4,6-Diphenyl-s-triazin-2-yl)-5-hexyloxyphenol; 2-[4-(Hexyloxy)-2-hydroxyphenyl]-4,6-diphenyl-1,3,5-triazine; 4,6-Diphenyl-2-(4-hexyloxy-2-hydroxyphenyl)-s-triazine; Tinuvin 1577; Tinuvin 1577ED; Tinuvin 1577FF; Tinuvin 167FF; Tinuvin 577FF; UV 1577. Grades: Highly Purified. CAS No. 147315-50-2. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| 2,4-Di-tert-butylphenol | 2,4-Di-tert-butylphenol (2,4-DTBP) is an orally active RXRα activator and a human estrogen receptor ligand with anti-inflammatory and antioxidant activities, which can induce apoptosis in tumor cells. 2,4-Di-tert-butylphenol can activate the RXRα subtype in LXRα/RXRα, PPARγ/RXRα, and hormone receptor β/RXR&alpha. 2,4-Di-tert-butylphenol also has antiviral and antifungal activities. 2,4-Di-tert-butylphenol can be used as an intermediate in the preparation of antioxidants and UV stabilizers, and is also used in the manufacture of medicines and fragrances [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: 2,4-DTBP. CAS No. 96-76-4. Pack Sizes: 10 mM * 1 mL; 100 g; 500 g. Product ID: HY-W014589. |  |
| 2- (5-tert-Butyl-2-hydroxyphenyl) benzotriazole | 2- (5-tert-Butyl-2-hydroxyphenyl) benzotriazole is a chemical reagent used in the synthesis of UV stabilizers in environmental waters.Used in the detection of UV light filters in sediment and sewage. Group: Biochemicals. Grades: Highly Purified. CAS No. 3147-76-0. Pack Sizes: 5g, 10g. Molecular Formula: C16H17N3O. US Biological Life Sciences. | Worldwide |
| 2- (5-tert-Butyl-2-hydroxyphenyl) benzotriazole-d9 | Isotope labelled 2- (5-tert-Butyl-2-hydroxyphenyl) benzotriazole is a chemical reagent used in the synthesis of UV stabilizers in environmental waters.Used in the detection of UV light filters in sediment and sewage. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C16H8D9N3O, Molecular Weight: 276.38. US Biological Life Sciences. | Worldwide |
| 2,6-Di-tert-butylphenol | 26-Di-tert-butylphenol is an organic compound with the structural formula 2,6-((CH3)3C)2C6H3OH. This colorless solid alkylated phenol and its derivatives are used industrially as UV stabilizers and Antioxidants for hydrocarbon-based products ranging from petrochemicals to plastics. Illustrative of its usefulness, it prevents gumming in aviation fuels. Group: Plastic additives. Alternative Names: 2,6-Di-t-butylphenol. CAS No. 128-39-2. Product ID: 2,6-ditert-butylphenol. Molecular formula: 206.32. Mole weight: C14H22O. CC(C)(C)C1=C(C(=CC=C1)C(C)(C)C)O. InChI=1S/C14H22O/c1-13(2, 3)10-8-7-9-11(12(10)15)14(4, 5)6/h7-9, 15H, 1-6H3. DKCPKDPYUFEZCP-UHFFFAOYSA-N. | |
| 2-Hydroxy-4-methoxybenzophenone | 2-Hydroxy-4-methoxybenzophenone (benzophenone-3) is commonly employed as broad-band UV-filter in sunscreen cosmetic products. It protects skin from the deleterious effects of the sun. It is one of the sunscreen constituent and its trace determination in water samples by solid-phase microextraction (SPME) and gas chromatography with flame ionization and mass spectrometric detection has been reported. Uses: Used as an ultraviolet light absorber and stabilizer (especially in plastics), photostabilizer for synthetic resins, and topical sunscreen agent. Synonyms: (2-hydroxy-4-methoxyphenyl)-phenylmethanone. Grades: > 98 %. CAS No. 131-57-7. Molecular formula: C14H12O3. Mole weight: 228.24. |  |
| Bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate | Bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate. Synonyms: UV-3765;TINUVIN 765;TINUVIN 292;DECANEDIOIC ACID BIS(1,2,2,6,6-PENTAMETHYLPIPERIDIN-4-YL)ESTER;BIS(1,2,2,6,6-PENTAMETHYL-4-PIPERIDYL) SEBACATE;BIS(1,2,2,6,6-PENTAMETHYL-4-PIPERIDINYL)SEBACATE METHYL 1,2,2,6,6-PENTAMETHYL-4-PIPERIDINYL SEBACATE;BIS(1, 2, 2, 6, 6-PENTAMETHYL-4-PIPERIDINYL)-SEBACATE;Bis(1, 2, 2, 6, 6, -Pentamethyl-4-Piperodinyl)-Sebacate. CAS No. 41556-26-7. Pack Sizes: 1 kg. Product ID: CDF4-0151. Molecular formula: C30H56N2O4. Category: Stabilizers and Thickeners. Product Keywords: Food Ingredients; Stabilizers and Thickeners; Bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate; CDF4-0151; 41556-26-7; C30H56N2O4; 255-437-1; 41556-26-7. Purity: 0.98. Color: White to Off-White Low-Melting. EC Number: 255-437-1. Physical State: Solid. Boiling Point: 220°C (26.7 Pa). Melting Point: 20°C. Product Description: TINUVIN 292 is a liquid hindered amine light stabilizer especially developed for coatings. It is an almost pure mixture of the two active ingredients below. It is this combination that keeps the product liquid, unlike the pure diester which tends to solidify, even at room temperature. The efficiency of TINUVIN 292 provides significantly extended lifetime to coatings by minimizing paint defects such as cracking and loss of gloss. |  |
| Chondroitinase AC from Flavobacterium heparinum, Recombinant | Chondroitinase AC from Flavobacteriun heparinum is an eliminase that degrades chondroitin sulfates A and C, but not chondroitin sulfate B. The enzyme cleaves, via an elimination mechanism, both sulfated and non-sulfated polysaccharide chains that contain (1?4)-linkages between hexosamines and glucuronic acid residues. The reaction yields oligosaccharide products, mainly disaccharides, with unsaturated uronic acids that can be detected by UV spectroscopy at 232 nm. Applications: Chondroitinase ac was shown to inhibit melanoma invasion and proliferation, endothelial proliferation, and angiogenesis. chondroitinase ac, but not chondroitinase b, has also been shown t..., and protease activities. ChnAC. Activity: >200 units/mg protein. Appearance: Powder. Storage: Store the product at -20?C. When stored properly and unopened at -20?C, the enzyme has a recommended retest date of 2 years. After reconstitution, the product may be kept at 4?C for 4 days, but it is recommended to store the solution in working aliquots at -20 ?C. Form: The enzyme is supplied as a lyophilized powder containing potassium phosphate, NaCl, and a stabilizer. Source: E. coli. Species: Flavobacterium heparinum. chondroitinase (ambiguous); chondroitin sulfate lyase; chondroitin AC eliminase; chondroitinase AC; ChnAC; 9047-57-8; EC 4.2.2.5. Cat No: NATE-1738. |  |
| Polyhydroxystearic Acid (CAS 27924-99-8) | Polyhydroxystearic acid (PHS) is a synthetic fatty acid used as an emulsifier and stabilizer in cosmetic products. It is commonly used in sunscreens to help prevent the formation of oily films on the skin and to improve the spreadability of the product. PHS also helps to increase the water resistance of sunscreens, making them more effective in protecting the skin from UV radiation. PHS is considered safe for use in cosmetic products by major regulatory bodies. It is non-toxic and non-irritating to the skin, and is biodegradable. Uses: 1. polyhydroxystearic acid (phs) is used as a dispersant and emulsifier in personal care products, such as sunscreens and makeup products. 2. phs helps to improve the texture and spreadability of the product by reducing the "whitening effect" commonly seen with physical sunscreens. 3. it also helps to stabilize the product and prevent separation of ingredients. 4. phs has anti-static properties that make it useful in hair care products to reduce frizz and flyaways. 5. it is biodegradable and considered environmentally friendly. 6. phs has low toxicity and is generally considered safe for use in cosmetic products. Group: Silicone replacements. CAS No. 27924-99-8. Appearance: white or off-white powder or flakes. Catalog: CI-HC-0085. | |
| Poly methyl vinyl ether maleic anhydride | In the solid state, poly(methylvinyl ether/maleic anhydride)copolymers are a white to off-white free flowing, odorless, hygroscopic powders. In solution, poly(methylvinyl ether/maleic anhydride) is a slightly hazy, odorless, viscous liquid. Synonyms: Butyl ester of poly(methylvinyl ether-co-maleic anhydride); calcium and sodium salts of poly(methylvinyl ether-co-maleic anhydride); Gantrez. Product ID: PE-0434. Molecular formula: (C4H2O3·C3H6O)x. Category: Bioadhesive Material; Color Dispersant; Emulsion Stabilizer; Film-forming Agents; Viscosity-increasing Agents. Product Keywords: Dispersion Excipients; Stabilizers; PE-0434; Poly methyl vinyl ether maleic anhydride; Bioadhesive Material; Color Dispersant; Emulsion Stabilizer; Film-forming Agents; Viscosity-increasing Agents; (C4H2O3·C3H6O)x; /. UNII: NA. Grade: Pharmceutical Excipients. Stability and Storage Conditions: Poly(methylvinyl ether/maleic anhydride) and related free acids are hygroscopic powders, and therefore excessive exposure to moisture should be avoided. Aqueous solutions exhibit decreases in viscosity upon exposure to UV light. Poly(methylvinyl ether/maleic anhydride) should be stored in a cool, dry place out of direct sunligh. Source and Preparation: Poly(methylvinyl ether/maleic anhydride) and copolymers are manufactured from methylvinyl ether and maleic anhydride. The S, ES, and MS grades of Gantrez are manufactured by | |
| UV-320 | UV-320 is a benzotriazole UV stabilizer, which is used to increase product stability and to prevent discolouration in various consumer and industrial goods such as plastics. Benzotriazole UV stabilizers are a pollutant for the aquatic environment and have been implicated as a potential stable and toxic ligands for aryl hydrocarbon receptor in human. Group: Biochemicals. Grades: Highly Purified. CAS No. 3846-71-7. Pack Sizes: 100g, 250g. Molecular Formula: C20H25N3O, Molecular Weight: 323.43. US Biological Life Sciences. | Worldwide |
| UV Absorber-UV 4050 | UV 4050 (124172-53-8) acts as a light stabilizer / UV absorber. It is suitable for the stabilization of polyolefins, particularly in thick-walled PP molding and PP fibers, as well as ABS, PS, PA and polyesters. Group: Uv resistant finishing agent. Alternative Names: N, N'-bis(2, 2, 6, 6-tetramethyl-4-piperidyl)-N, N'-diformylhexamethylenediamine. CAS No. 124172-53-8. Molecular formula: C26H50N4O2. Mole weight: 450.7. Catalog: ACM124172538. | |
| UV Absorber-UV B 75 | UV B 75 is a synergistic blend of 20% AN 1135, 40% UV 571 and 40% LS 292. Acts as a light and heat stabilizer agent. Group: Uv resistant finishing agent. Alternative Names: 2-(2H-Benzothiazol-2-yl)-6-(dodecyl)-4-methylphenol. CAS No. 41556-26-7/82919-37-7. Molecular formula: C30H56N2O4 / C21H39NO4. Mole weight: 508.78 / 369.54. Catalog: ACM41556267-3. | |
| 2-(2H-Benzotriazol-2-yl)-4,6-di-tert-pentylphenol | 2-(2H-Benzotriazol-2-yl)-4,6-di-tert-pentylphenol is an ultraviolet light absorber (UVA) of the hydroxyphenylbenzotri azole class, which imparts outstanding light stability to plastics and other organic substrates. Group: Biochemicals. Grades: Highly Purified. CAS No. 25973-55-1. Pack Sizes: 1g, 5g. Molecular Formula: C22H29N3O. US Biological Life Sciences. | Worldwide |
| 2-(2H-Benzotriazol-2-yl)-4,6-di-tert-pentylphenol-d12 | Isotope labelled 2-(2H-Benzotriazol-2-yl)-4,6-di-tert-pentylphenol is an ultraviolet light absorber (UVA) of the hydroxyphenylbenzotri azole class, which imparts outstanding light stability to plastics and other organic substrates. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C22H17D12N3O, Molecular Weight: 363.56. US Biological Life Sciences. | Worldwide |
| 2-Hydroxy-4-(octyloxy)benzophenone | 2-Hydroxy-4-(octyloxy)benzophenone (HOBP) is a UV based absorber that has 2-hydroxybenzophenone as a functional group. It can be used to enhance the light fastness of polymers using UV absorbers with sulfur and phosphorus compounds. Uses: Hobps are uv absorbers for insulating plastics, which can be incorporated with active layers to increase the stabilization of organic solar cells (oscs). it may be incorporated in parylene c films to enhance the light stability, which can be potentially used as a moisture transfer membrane for electronic boards and photovoltaics. Group: Plastic additives. Alternative Names: [2-Hydroxy-4-(octyloxy)phenyl]phenylmethanone, 2-Benzoyl-5-octyloxyphenol, 4-(Octyloxy)-2-hydroxybenzophenone. CAS No. 1843-05-6. Pack Sizes: Packaging 100 g in glass bottle. Product ID: (2-hydroxy-4-octoxyphenyl)-phenylmethanone. Molecular formula: 326.43. Mole weight: CH3(CH2)7OC6H3(OH)COC6H5. CCCCCCCCOc1ccc(c(O)c1)C(=O)c2ccccc2. 1S / C21H26O3 / c1-2-3-4-5-6-10-15-24-18-13-14-19 (20 (22) 16-18) 21 (23) 17-11-8-7-9-12-17 / h7-9, 11-14, 16, 22H, 2-6, 10, 15H2, 1H3. QUAMTGJKVDWJEQ-UHFFFAOYSA-N. 99%. | |
| β-Xylosidase, thermostable, Recombinant | Releases reducing sugars from birchwood xylan (X0502), also catalyzes the hydrolysis of 4-methylumbelliferyl-β-D-cellobioside and 4-methylumbelliferyl-β-D-glucopyranoside. This enzyme does not possess endo-xylanase, arabinoxylanase or β-glucanase activities. β-Xylosidase undergoes post-translation glycosylation which has been shown to be critical for its proper activity and stability. Deglycosylation altered the the optimum temperature and pH for activity and decreased its thermostability. Group: Enzymes. Synonyms: β-Xylosidase; β-Xylosidase, thermostable; 9025-53-0. CAS No. 9025-53-0. Purity: > 20 mg protein/mL (UV) > 90% (SDS-PAGE). β-Xylosidase. Mole weight: mol wt 81 kDa. Activity: > 35 units/mg protein. Storage: 2-8°C. Form: liquid, Supplied as a solution in 50 mM Tris-HCl, pH 8.0, 100 mM NaCl, and 25% glycerol. Source: E. coli. β-Xylosidase; β-Xylosidase, thermostable; 9025-53-0. Cat No: NATE-0789. | |
| Bis(3-Triethoxysilylpropyl)Amine | It is colorless transparent liquid, soluble in a variety of organic solvents. Uses: It can lead to colorless low-viscosity pu prepolymers with improved uv stability and reduced yellowing tendency of sealants. Group: Siloxanes. Alternative Names: Bis[3-(Triethoxysilyl)Propyl]Amine. CAS No. 13497-18-2. Molecular formula: C18H43NO6Si2. Mole weight: 425.71. Appearance: Transparent liquid. Purity: >95%. IUPACName: 3-triethoxysilyl-N-(3-triethoxysilylpropyl)propan-1-amine. Canonical SMILES: CCO[Si] (CCCNCCC[Si] (OCC) (OCC)OCC) (OCC)OCC. Density: 0.973 g/mL. ECNumber: 236-818-1. Catalog: ACM13497182. | |
| Bis(tetrabromophthalimide) | It has outstanding thermal and UV stability. lts white color allows use incolor-sensitive applications. lts thermal stability allows use in engineering resins likepolyesters and polyamides. It is also non-blooming. This feature allows use in such critical applications aspolyolefin films where good heat sealability is required. lts excellent wet electricalproperties also make it ideal for wire and cable applications. It provides premium performance in a wide range of applications. Such as polyolefins, high-impactpolystyrene (HIPS), thermoplastic polyesters (PBT, PET,etc), polycarbonate and elastomers. Group: Brominated flame retardant. Alternative Names: 1,2-Bis(tetrabromophthalimido)ethane. CAS No. 32588-76-4. Molecular formula: C18H4O4N2Br8. Mole weight: 951.5. Appearance: white powder. Catalog: ACM32588764-1. | |
| Chondroitinase ABC from Proteus vulgaris, Recombinant | Chondroitinase ABC cleaves, via an elimination mechanism, sulfated and non-sulfated polysaccharide chains containing 1-4 linkages between hexosamines and glucuronic acid residues. The reaction yields oligosaccharide products (mainly disaccharides) containing unsaturated uronic acids which can be detected by UV spectroscopy at 232 nm. The enzyme is active on chondroitin sulfates A and C, chondroitin sulfates B (dermatan sulfate), chondroitin and hyaluronic acid. Applications: Determination of contents of chondroitin sulfates by hplcprocessing animal tissues before further investigationspreparation of chondroitin and hyaluronic acid derived unsaturated disaccharidespreparation of hyaluronic acid derived unsaturated disaccharide. Group: Enzymes. Synonyms: EC 4.2.2.4, chondroitinase; ch. Enzyme Commission Number: EC 4.2.2.20. CAS No. 9024-13-9. Chondroitinase ABC. Mole weight: 117.3 kDa. Activity: > 100 IU/mg (substrate: chondroitin sulfate A). Stability: Expiration is at least 12 months from manufacturing date, kept at -20 °C. Source: E.coli. Species: Proteus vulgaris. EC 4.2.2.4, chondroitinase; chondroitin ABC eliminase; chondroitinase ABC; chondroitin ABC lyase; chondroitin sulfate ABC lyase; ChS ABC lyase; chondroitin sulfate ABC endoeliminase; chondroitin sulfate ABC endolyase; ChS ABC lyase I; 9024-13-9. Cat No: NATE-1949. | |
| -COOH Modified Upconverting Nanoparticles (UV light) | -COOH Modified Upconverting Nanoparticles (UV light). Uses: Up conversion nanoparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodynamic therapy, and photoactivated drug activation. Group: Sio2-cooh modified upconverting nanoparticles. Pack Sizes: 10 mg/20 mg. | |
| Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide | Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO) is a monoacylphosphine oxide based photoinitiator that can be incorporated in a variety of polymeric matrixes for efficient curing and color stability of the resin. Uses: Tpo can be used in the photo-crosslinking of pmma composite, which can further be used as a gate insulator in organic thin film transistors (otfts). it can also be used in the formation of uv curable urethane-acrylate coatings. it may also be used in the photoinduced reaction for the formation of organophosphine compounds, which potentially find their usage as ligands with metal catalysts and reagents. Alternative Names: 2,4,6-Trimethylbenzoylphenyl phosphinate, (Diphenylphosphoryl) (mesityl)methanone, (2,4,6-Trimethylbenzoyl)diphenylphosphine oxide. CAS No. 75980-60-8. Molecular formula: C22H21O2P. Mole weight: 348.37. Appearance: White or cream powder. Purity: 95%+. IUPACName: Diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone. Canonical SMILES: CC1=CC (=C (C (=C1)C)C (=O)P (=O) (C2=CC=CC=C2)C3=CC=CC=C3)C. Density: 1.17 g/cm³. ECNumber: 278-355-8. Catalog: ACM75980608-2. | |
| Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide | Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO) is a monoacylphosphine oxide based photoinitiator that can be incorporated in a variety of polymeric matrixes for efficient curing and color stability of the resin. Uses: Tpo can be used in the photo-crosslinking of pmma composite, which can further be used as a gate insulator in organic thin film transistors (otfts). it can also be used in the formation of uv curable urethane-acrylate coatings. it may also be used in the photoinduced reaction for the formation of organophosphine compounds, which potentially find their usage as ligands with metal catalysts and reagents. Group: Polymerization reagents. Alternative Names: 2,4,6-Trimethylbenzoylphenyl phosphinate, (Diphenylphosphoryl) (mesityl)methanone, (2,4,6-Trimethylbenzoyl)diphenylphosphine oxide. CAS No. 75980-60-8. Pack Sizes: Packaging 10, 50 g in poly bottle. Product ID: Diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone. Molecular formula: 348.37. Mole weight: C22H21O2P. CC1=CC (=C (C (=C1)C)C (=O)P (=O) (C2=CC=CC=C2)C3=CC=CC=C3)C. InChI=1S/C22H21O2P/c1-16-14-17 (2) 21 (18 (3) 15-16) 22 (23) 25 (24, 19-10-6-4-7-11-19) 20-12-8-5-9-13-20/h4-15H, 1-3H3. VFHVQBAGLAREND-UHFFFAOYSA-N. 95%+. | |
| Fluoride-free UV-assisted etching of multilayer Mo2C MXene | The new UV-assisted selective etching method can etch Ga atoms in the Mo2Ga2C precursor to obtain fluorine-free Mo2C MXene and avoid the use of toxic and highly corrosive acids. The obtained MXene exhibits a unique 2D graphene-like structure and high purity. When used as a negative electrode material for rechargeable batteries, it exhibits outstanding rate performance and cycle stability. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. 0.99. | |
| Hokkaido Orange | A manufactured pigment Excellent UV Stability Suitable for all mediums Not Cosmetic or Pharmaceutical Grade Lime and Cement Color Stable. Group: Pigments. CAS No. 85536-73-8. Catalog: ACM85536738. | |
| Hops Flower Extract (Standard) | Hops are the female flower cones, also known as strobiles, of the hop plant (Humulus lupulus). The hop is part of the family Cannabaceae, which also includes the genus Cannabis (hemp). They are used primarily as a flavoring and stability agent in beer, though hops are also used for various purposes in other beverages and herbal medicine. Applications: It can inhibit the growth of various bacteria. such as bacillus anthracis, bacillus, corynebacterium diphtheriae, diplococcus pneumoniae and staphylococcus aureusit can also help to stimulate appetite , dispel flatulence, and relieve intestinal cramps. Group: Others. CAS No. 6754-58-1. Purity: 4.0% Flavones UV. Mole weight: 354.14. Hops Flower Extract (Standard); 6754-58-1; C21H22O5. Cat No: EXTW-018. | |
| Mesoporous SiO2 coated Upconverting Nanoparticles(UV light) | Mesoporous SiO2 coated Upconverting Nanoparticles(UV light). Uses: Up conversion nanoparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodynamic therapy, and photoactivated drug activation. Group: Mesoporous sio2 coated upconverting nanoparticles. Pack Sizes: 10 mg/20 mg/50 mg. | |
| Monte Carlo Blue | Manufactured color Good UV Stability Suitable for all mediums Not Cosmetic or Pharmaceutical Grade Not Lime or Cement Color Stable New manufacturer, smoother mixing. Group: Pigments. CAS No. 147-14-87. Molecular formula: C32H16N8CuCAS+BASO4. Catalog: ACM1471487. | |
| Native Flavobacterium heparinum Chondroitinase B | Chondroitinase B cleaves, via an elimination mechanism, polysaccharide chains containing 1-4 linkages between hexosamines and iduronic acid residues in dermatan sulfate (chondroitin B).The reaction yields oligosaccharide products (mainly disaccharides) containing unsaturated uronic acids which can be detected by UV spectroscopy at 232 nm. Applications: Research reagent (glycobiology, preparation of oligosaccharide libraries from dermatan sulfate).determination of contents of chondrotin sulfates by hplc. Group: Enzymes. Synonyms: Chondroitinase B; EC 4.2.2.19; chondroitin B lyase; ChonB; ChnB. Enzyme Commission Number: EC 4.2.2.19. CAS No. 52227-83-5. ChonB. Mole weight: 55 kDa. Activity: >200 IU/mg (substrate: dermatan sulfate). Stability: 12 months frozen at -20°C in aqueous buffers containing sodium phosphate and sucrose 5%. Source: Flavobacterium heparinum. Chondroitinase B; EC 4.2.2.19; chondroitin B lyase; ChonB; ChnB. Cat No: NATE-1950. | |
| -NH2 modified Upconverting Nanoparticles(UV light) | -NH2 modified Upconverting Nanoparticles(UV light). Uses: Up conversion nanoparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodynamic therapy, and photoactivated drug activation. Group: Sio2-nh2 modified upconverting nanoparticles. Pack Sizes: 10 mg/20 mg. | |
| Oil dispersible upconverting nanoparticles (UV light) | Oil dispersible upconverting nanoparticles (UV light). Uses: Up conversion noparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodymic therapy, and photoactivated drug activation. Group: Oil dispersible upconverting nanoparticles. Pack Sizes: 50 mg. | |
| PbS core-type quantum dots | PbS core-type quantum dots. Uses: Our pbs quantum dots have a fully crystalline inorganic core and are organically stabilized with an oleic acid coating, which makes their surface hydrophobic in nature. they exhibit high colloidal and thermal stability, as well as strong emissions with narrow fluorescence bands, owing to their small particle size distributions. these particles absorb all light in the uv, vis and nir, up to 900 nm. their size-dependent absorption and emission properties make them suitable for different applications: such as, absorber materials in photovoltaics, detectors and photodiodes, and phosphors in ir-emitters (solid state lighting, ssl), among many others. Group: Quantum dots. | |
| PEG -COOH Modified Upconverting Nanoparticles (UV light) | PEG -COOH Modified Upconverting Nanoparticles (UV light). Uses: Up conversion nanoparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodynamic therapy, and photoactivated drug activation. Group: Peg-cooh modified upconverting nanoparticles. Pack Sizes: 10 mg/20 mg. | |
| PEG modified Upconverting Nanoparticles(UV light) | PEG modified Upconverting Nanoparticles(UV light). Uses: Up conversion nanoparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodynamic therapy, and photoactivated drug activation. Group: Peg modified upconverting nanoparticles. Pack Sizes: 8 mg/16 mg. | |
| PEG-NH2 Modified Upconverting Nanoparticles (UV light) | PEG-NH2 Modified Upconverting Nanoparticles (UV light). Uses: Up conversion nanoparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodynamic therapy, and photoactivated drug activation. Group: Peg-nh2 modified upconverting nanoparticles. Pack Sizes: 10 mg/20 mg. | |
| Phenoxy-terminated carbonate oligomer of Tetrabromobisphenol A | It is a brominated, aromatic Flame Retardant for thermoplastic resin systems. It is a white powder, offers excellent thermal stability, good UV stability and color.unique combination of properties makes it a suitable flame retardant in PBT, PET, PBT/PET blends, PC, ABS, ABS/PC blends, Polysulfone and SAN. The UV stability allows it to be formulated for applications subjected to indoor fluorescent and casual outdoor sunlight exposure. In addition, the high purity makes it a solid choice for applications requiring excellent electrical and thermal properties. Uses: Mainly use for pbt, pet, pbt/pet blends, pc, abs, abs/pc blends, polysulfone and san. Group: Brominated flame retardant. CAS No. 71342-77-3. Molecular formula: (C7H2Br3O2). (C16H10Br4O3)n. (C6H2Br3O). Appearance: White Powder. Catalog: ACM71342773-1. | |
| Quaterrylene | A promising candidate for organic electronic applications because it absorbs a broad spectrum of UV and visible light, while possessing excellent thermal and oxidative stability and a low HOMO-LUMO band gap. Organic Electronics Photovoltaic Components Graphene Nanoribbons Electroactive Polymers. Group: Organic & printed electronics. Alternative Names: Benzo[1,2,3-cd: 4,5,6-c'd']diperylene. CAS No. 188-73-8. Molecular formula: C40H20. Mole weight: 500.59. IUPACName: undecacyclo[20.12.2.22, 5.16, 10.123, 27.03, 18.04, 15.019, 35.032, 36.014, 38.031, 37]tetraconta-1(35), 2, 4, 6, 8, 10(38), 11, 13, 15, 17, 19, 21, 23, 25, 27(37), 28, 30, 32(36), 33, 39-icosaene. Canonical SMILES: C12=CC=CC (C3=C (C4=CC=C5C6=CC=C (C7=CC=C8) C9=C (C%10=C7C8=CC=C%10) C=CC%11C96) C5=C%11C=C3) =C1C4=CC=C2. Catalog: ACM188738. | |
| Quaterrylene | Quaterrylene. Uses: A promising candidate for organic electronic applications because it absorbs a broad spectrum of uv and visible light, while possessing excellent thermal and oxidative stability and a low homo-lumo band gap. organic electronics photovoltaic components graphene nanoribbons electroactive polymers. Group: Carbon nano materials organic light-emitting diode (oled) materials. Alternative Names: Benzo[1,2,3-cd: 4,5,6-c'd']diperylene. CAS No. 188-73-8. Pack Sizes: 25 mg in poly bottle. Product ID: undecacyclo[20.12.2.22, 5.16, 10.123, 27.03, 18.04, 15.019, 35.032, 36.014, 38.031, 37]tetraconta-1(35), 2, 4, 6, 8, 10(38), 11, 13, 15, 17, 19, 21, 23, 25, 27(37), 28, 30, 32(36), 33, 39-icosaene. Molecular formula: 500.59. Mole weight: C40H20. C12=CC=CC (C3=C (C4=CC=C5C6=CC=C (C7=CC=C8) C9=C (C%10=C7C8=CC=C%10) C=CC%11C96) C5=C%11C=C3) =C1C4=CC=C2. 1S / C40H22 / c1-5-21-6-2-10-24-28-14-18-32-34-20-1 6-30-26-12-4-8-22-7-3-11-25 (36 (22) 26) 29-15-19-33 (40 (34) 38 (29) 30) 31-17-13-27 (37 (28) 39 (31) 32) 23 (9-1) 35 (21) 24 / h1-20, 31, 39H, BWASZFNXSFVOCT-UHFFFAOYSA-N. BWASZFNXSFVOCT-UHFFFAOYSA-N. | |
| SiO2 coated Upconverting Nanoparticles(UV light) | SiO2 coated Upconverting Nanoparticles(UV light). Uses: Up conversion nanoparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodynamic therapy, and photoactivated drug activation. Group: Sio2 coated upconverting nanoparticles. Pack Sizes: 10 mg/20 mg/50 mg. | |
| TiO2 coated Upconverting Nanoparticles(UV light) | TiO2 coated Upconverting Nanoparticles(UV light). Uses: Up conversion nanoparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodynamic therapy, and photoactivated drug activation. Group: Tio2 coated upconverting nanoparticles. Pack Sizes: 10 mg/20 mg/50 mg. | |
| Tris(tribromoneopentyl)phosphate | Tris(tribromoneopentyl) Phosphate is an additive Flame Retardant developed for applications such as PP and HIPS to reach class V-2 according to the UL 94 standard, with outstanding UV and light stability. It was designed initially to provide an answer in the fast growing and developing field of PP, where the market was in need of a new more sophisticated flame retardant. The combination of both a high bromine content (70%) and phosphorous (3%) contributes to its excellent flame retardant efficiency. The chemical structure of the brominated part is responsible for its excellent UV and light stability leading to a good appearance of the molded part. The high melting temperature (181?C) permits production of highly filled masterbatch concentrates. In addition, as it is melt blendable and melts at the processing temperature of PP, it is easy to process and can improve flowability. It solves the previously unanswered problem of blooming in flame retardant grades of PP. Uses: Mainly use for abs (v-2), adhesives, hips (v-2), pc/pbt, pp and copolymers, xps and so on. Group: Bromine series. Alternative Names: Tris(tribromoneopenthyl)phosphate; TRIS (TRI BROMONEOPENTYL) PHOSPHATE;2,2-bis-(bromomethyl)-3-bromo-1-propanol phosphate;1-PROPANOL, 3-BROMO-2,2-BIS(BROMOMETHYL)-, PHOSPHATE(3:1);3-bromo-2,2-bis(bromomethyl)-1-propanophosphate(3:1);TRIS (TRI BROMONEOPENTHYL) PHOSPHATE TTBNPP;1-Propanol, 3-bromo-2,2-bis(bromo | |
| Tris(tribromoneopentyl)phosphate | Tris(tribromoneopentyl) Phosphate is an additive Flame Retardant developed for applications such as PP and HIPS to reach class V-2 according to the UL 94 standard, with outstanding UV and light stability. It was designed initially to provide an answer in the fast growing and developing field of PP, where the market was in need of a new more sophisticated flame retardant. The combination of both a high bromine content (70%) and phosphorous (3%) contributes to its excellent flame retardant efficiency. The chemical structure of the brominated part is responsible for its excellent UV and light stability leading to a good appearance of the molded part. The high melting temperature (181?C) permits production of highly filled masterbatch concentrates. In addition, as it is melt blendable and melts at the processing temperature of PP, it is easy to process and can improve flowability. It solves the previously unanswered problem of blooming in flame retardant grades of PP. Uses: Mainly use for abs (v-2), adhesives, hips (v-2), pc/pbt, pp and copolymers, xps and so on. Group: Polymers. Alternative Names: Tris(tribromoneopenthyl)phosphate; TRIS (TRI BROMONEOPENTYL) PHOSPHATE; 2,2-bis-(bromomethyl)-3-bromo-1-propanol phosphate; 1-PROPANOL, 3-BROMO-2,2-BIS(BROMOMETHYL)-, PHOSPHATE(3:1); 3-bromo-2,2-bis(bromomethyl)-1-propanophosphate(3:1); TRIS (TRI BROMONEOPENTHYL) PHOSPHATE TTBNPP; 1-Propanol, 3-bromo-2,2-bis(bromom | |
| upconverting nanoparticles(UV light) | upconverting nanoparticles(UV light). Uses: Up conversion noparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodymic therapy, and photoactivated drug activation. Group: Upconverting nanoparticles. Pack Sizes: 50 mg. | |
| UV Absorber-UV 3030 | UV 3030 (178671-58-4) is an UV Absorber that can be used to stabilize highly transparent polymers with high extrusion temperatures. Group: Uv resistant finishing agent. Alternative Names: 1, 3-bis-((2-cyano-3, 3-diphenylacryloyl) oxy)-2, 2-bis-(((2-cyano-3, 3-diphenylacryloyl) oxy) methyl)-propane. CAS No. 178671-58-4. Molecular formula: C69H48N4O8. Mole weight: 1061.14. Catalog: ACM178671584-1. | |
| UV Absorber-UV 360 | A very low volatile product of hydroxyphenyl benzotriazole class, imparting outstanding light stability to a variety of polymers. Group: Uv resistant finishing agent. Alternative Names: Phenol, 2,2-methylene-bis(6-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)). CAS No. 103597-45-1. Molecular formula: C41H50N6O2. Mole weight: 658.87. Catalog: ACM103597451. | |
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