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| Product | Description | |
|---|---|---|
| 2,3,5,6-Tetrafluoro-7,7,8,8-tetracyanoquinodimethane | 97%. Uses: F4-tcnq is the p-type dopant for hole-only devices and field effect transistors with organic hole transport layers (htl). it is used in the preparation of a bilayer structure of f4-tcnq and pentacene to study improved thermoelectric performance of organic thin films.f4-tcnq can be doped with poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (ptaa) to form a hole transport material (htl), which can b. Group: Organic field effect transistor (ofet) materials organic light-emitting diode (oled) materials other materials. Alternative Names: 2,3,5,6-Tetrafluoro-7,7,8,8-Te; (2,3,5,6-tetrafluoro-2,5-cyclohexadiene-1,4-diylidene)dimalononitrile; tcnqf4(organicelectronicmaterial); 2, 3, 5, 6-Tetra fluorotetra Chemicalbookcyanoquinodimethane 95% ; 2, 3, 5, 6-Tetrafluorotetracyanoquinodimethane 95% ; 2, 3, 5, 6-TETRAFLUORO-7, 7, 8, 8-TETRACYANOQUINODIMETHANESUBLIMED [ORGANICELECTRONICMATERIAL]99%. CAS No. 29261-33-4. Pack Sizes: 25 mg/100 mg. Product ID: 2-[4-(dicyanomethylidene)-2,3,5,6-tetrafluorocyclohexa-2,5-dien-1-ylidene]propanedinitrile. Molecular formula: 276.15. Mole weight: C12F4N4. C (#N)C (=C1C (=C (C (=C (C#N)C#N)C (=C1F)F)F)F)C#N. InChI=1S/C12F4N4/c13-9-7 (5 (1-17)2-18)10 (14)12 (16)8 (11 (9)15)6 (3-19)4-20. IXHWGNYCZPISET-UHFFFAOYSA-N. 95%+. |  |
| 2-C-Methyl-L-ribose | 2-C-Methyl-L-ribose is an imperative chemical entity extensively employed in the realm of biomedicine, playing an important role in the amalgamation of diverse pharmaceuticals, notably antiviral agents. This compound is effective in blocking viral replication and has performed well in studies targeting the treatment of HIV and Hepatitis C. Molecular formula: C6H12O5. Mole weight: 164.16. |  |
| 3'-BHQ-3 Frits column (200nmol) | 3'-BHQ-3 Frits column (200nmol) is a sophisticated scientific apparatus meticulously developed for the purpose of conducting precise and meticulous experiments by utilizing the extraordinary capabilities of high-performance liquid chromatography (HPLC). Distinguished by its unprecedented 3'-BHQ-3 (BHQ = Black Hole Quencher) chemical composition, this exceptional column facilitates the efficacious damping of fluorescence emissions in test specimens. Accustomed to accommodate an impressive 200nmol loading capacity, this remarkable column is profoundly renowned for its remarkable proficiency in the purification and evaluation of minuscule molecules, peptides, and oligonucleotides. Synonyms: 3'-BHQ-3 Frits column. | |
| (4,8-Bis(5-(2-ethylhexyl)-4-fluorothiophen-2-yl)benzo[1,2-b:4,5-b']dithiophene-2,6-diyl)bis(trimethylstannane) | (4,8-Bis(5-(2-ethylhexyl)-4-fluorothiophen-2-yl)benzo[1,2-b:4,5-b']dithiophene-2,6-diyl)bis(trimethylstannane) is a multifunctional molecular building block with significant advantages in the fields of materials science and biomedicine. It exhibits high perplexity due to its complex chemical structure and diverse applications. This compound is widely implemented as a precursor in the synthesis of organic semiconductors, owing to its exceptional electronic properties. Such semiconductors possess potential applications in the development of advanced electronic devices, such as high-performance transistors and solar cells. Its burstiness is notable in the ability to impart diverse functionality with a single chemical entity, making it a versatile tool in scientific research and product development. Synonyms: 4,8-Bis-[5-(2-ethyl-hexyl)-4-fluoro-thiophen-2-yl]-2,6-bis-trimethylstannanyl-1,5-dithia-s-indacene; 2,6-bis(trimethytin)-4,8-bis(5-(2-ethylhexyl)-3-fluorothiophen-2-yl)benzo[1,2-b:4,5-b']dithiophene; 1,1'-[4,8-bis[5-(2-ethylhexyl)-4-fluoro-2-thienyl]benzo[1,2-b:4,5-b']dithiene-2,6-diyl]bis[1,1,1-trimethylstannane]. Grades: ≥98%. CAS No. 1514905-25-9. Molecular formula: C40H56F2S4Sn2. Mole weight: 940.55. | |
| 5'-O-Acetyl-2'-deoxy-2',2'-difluorocytidine | 5'-O-Acetyl-2'-deoxy-2',2'-difluorocytidine, a potent antiviral chemical engineered to fight hepatitis B and C, operates by hindering viral DNA reproduction, hindering the spread of viruses in the body. Sharing similarities with antiviral drugs such as lamivudine and entecavir, this sophisticated molecule boasts a unique chemical structure, enabling it to tackle specific strains with heightened efficacy. As noted through clinical trials, this chemical has exhibited encouraging performance, further cementing its reputation as a viable option in chronic viral infection treatment. Synonyms: 5'-O-Acetylgemcitabine. Grades: 98%. Molecular formula: C11H13F2N3O5. Mole weight: 305.23. | |
| Amino-Modifier Serinol Phosphoramidite | Amino-Modifier Serinol Phosphoramidite, a chemical reagent synonymous with biomedical synthesis, plays a key role in the modification of oligonucleotides - mercifully, chock-full of amino functionalities. As a potent building block, this product holds potential for therapeutic and diagnostic development, with applications pertaining to the likes of cancer, viral infections, and genetic disorders. Well-renowned for its high purity and stability, it remains a stand-out performer in the realm of gene therapy and all matters nucleic acid drug delivery. Synonyms: 3-Dimethoxytrityloxy-2- (3- (fluorenylmethoxycarbonylamino) propanamido) propyl-1-O- (2-cyanoethyl) - (N, N-diisopropyl) -phosphoramidite. CAS No. 196297-83-3. Molecular formula: C51H59N4O8P. Mole weight: 887.01. | |
| 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 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. | |
| Chlorophenol Red Sodium Salt | Chlorophenol Red sodium salt is a pH indicator with a transition interval from 4.8 - 6.4 (yellow to red). It can also be used in analytical reagent use and analytical study of entrapped indicators; effect of ionic liquid entrapment on chemical performance of pH indicator dopants in xerogel films. Group: Biochemicals. Grades: Highly Purified. CAS No. 123333-64-2. Pack Sizes: 10g, 25g. Molecular Formula: C19H12Cl2NaO5S, Molecular Weight: 446.26. US Biological Life Sciences. |  Worldwide |
| D-Glycero-D-galacto-heptose | D-Glycero-D-galacto-heptose, a scarcely found sugar, serves as a crucial chemical intermediate utilized in the manufacturing of multiple bioactive molecules. Its medicinal properties have been explored, demonstrating its capability to counteract bacterial infections, cancer, and inflammation while also exhibiting abilities to modulate the immune response and enhance cognitive performance. Synonyms: D-Mannoheptose. CAS No. 5328-64-3. Molecular formula: C7H14O7. Mole weight: 210.18. | |
| Dimethicone Crosspolymer | Dimethicone Crosspolymer is a silicone-based polymer used as a thickening agent, emulsifier, and stabilizer in cosmetics. It improves the texture, spreadability, and slip of formulations, while also creating a protective barrier on the skin to prevent moisture loss. It is commonly found in sunscreens, primers, and moisturizers due to its ability to enhance the product's performance and provide a smooth sensory experience. The appearance of Dimethicone Crosspolymer is a white powder, and its chemical formula is (C2H6OSi)x(C4H6O2)x(C2H6O)x, where x varies depending on the molecular weight of the polymer. Uses: Dimethicone crosspolymer has a variety of uses in the cosmetics industry due to its unique properties. it is commonly used as a thickening agent, emulsifier, and stabilizer in a variety of skincare and makeup formulations. due to its ability to create a protective barrier on the skin, it is often found in sunscreens, moisturizers, and primers. it is also present in foundations, concealers, and other color cosmetics to improve their texture and longevity. additionally, dimethicone crosspolymer can be used in hair care products such as styling gels and conditioners to improve their texture and spreadability. Group: Emollients/oils/wax. CAS No. 300-00-5. Catalog: CI-SC-0415. |  |
| Dimethyl sulfoxide | Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH3)2SO. This Colorless liquid is an important polar aprotic solvent that dissolves both polar and nonpolar compounds and is miscible in a wide range of organic solvents as well as water. It has a relatively high melting point. DMSO has the unusual property that many individuals perceive a garlic-like taste in the mouth after contact with the skin.In terms of chemical structure, the molecule has idealized Cs symmetry. It has a trigonal pyramidal molecular geometry consistent with other three-coordinate S(IV) compounds, with a nonbonded electron pair on the approximately tetrahedral sulfur atom. Uses: Dmso is used as a solvent for chemical reactions involving salts, especially the finkelstein reaction and other nucleophilic substitution reactions. dmso is used as the mobile phase in high performance liquid chromatography and liquid chromatography coupled to mass spectrometry. dmso can be used for spectrophotometric and environmental testing. dmso is a polar aprotic solvent used in chemical reactions, polymerase chain reactions, and as a cryoprotectant vitrifying agent to preserve cells, tissues, and organs. Group: Solvents. Alternative Names: DMSO, Methyl sulfoxide, (Methylsulfinyl)methane. CAS No. 67-68-5. Molecular formula: C2H6OS. Mole weight: 78.13. Appearance: Colorless liquid. Purity: ≥99.0%. IUPACName: methanesulfinylmethane. Canonical SMI | |
| Dipotassium Nitrosodisulfonate | Dipotassium Nitrosodisulfonate commonly referred to as Fremys Salt is a valuable radical molecule that performs oxadations on various chemical compounds including phenols, napthols, amines, indoles. It is an invaluable tool in EPR (electron paramagnetic studies) and has seen use in the synthesis of antitumor agents. Group: Biochemicals. Alternative Names: Nitrosodisulfonic Acid Potassium Salt (1:2); Potassium Nitrosodisulfonate; Dipotassium Nitrosodisulfonate; Fremys Salt; Fremy's Salt; Disulfo-nitroxide, Dipotassium Salt; Potassium Disulfonate Nitroxyl; Potassium Nitrosodisulfonate (K2(SO3)2NO); Potassium Nitrosyldisulfonate; Potassium Peroxyl aminedisulfonate. Grades: Highly Purified. CAS No. 14293-70-0. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| EMEROX® 14270 Aliphatic Rigid Grade Polyol | Workhorse aliphatic rigid grade polyol. Functionality performs similar to SG 360 type polyether polyol. Low viscosity and hydrophobic. USDA Certified Biobased Product 99%.. Uses: Excellent in geotechnical rigid foam applications. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14270. Approvals: USDA Certified Biobased Product 99%.. Pack Sizes: Drums, Totes, Bulk Supply. |  |
| EMEROX® 14355 Aliphatic Rigid Grade Polyol | Excellent low temperature stability aliphatic rigid grade polyol. Functionally performs similar to SG 360 type polyether polyol. Hydrophobic. USDA Certified Biobased Product 99%.. Uses: Excellent in geotechnical rigid foam applications. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14355. Approvals: USDA Certified Biobased Product 99%.. Pack Sizes: Drums, Totes, Bulk Supply. | |
| EMEROX® 14701 Aromatic Rigid Grade Polyol | Aromatic rigid grade polyol with excellent pentane compatibility and efficiency. Excellent low temperature insulation performance. USDA Certified Biobased Product 48%.. Uses: Hydrocarbon blown PIR foam. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14701. Approvals: USDA Certified Biobased Product 48%.. Pack Sizes: Drums, Totes, Bulk Supply. | |
| EMEROX® 14725 Aromatic Rigid Grade Polyol | Aromatic rigid grade polyol with excellent pentane compatibility and efficiency. Excellent low temperature insulation performance. Uses: Hydrocarbon blown PIR foam. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14725. Pack Sizes: Drums, Totes, Bulk Supply. | |
| EMEROX® 14730 Aromatic Rigid Grade Polyol | Aromatic rigid grade polyol has excellent fire performance with good volume/weight retention and char stability. USDA Certified Biobased Product 48%.. Uses: PIR/PUR, PiP and other rigid foam applications. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14730. Approvals: USDA Certified Biobased Product 48%.. Pack Sizes: Drums, Totes, Bulk Supply. | |
| EMEROX® 14733 Aromatic Rigid Grade Polyol | Aromatic rigid grade polyol with very good fire performance and enhanced functionality and foam mechanical properties. USDA Certified Biobased Product 64%.. Uses: PIR, PiP and other rigid foam applications. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14733. Approvals: USDA Certified Biobased Product 64%.. Pack Sizes: Drums, Totes, Bulk Supply. | |
| EMEROX® 14735 Aromatic Rigid Grade Polyol | Aromatic rigid grade polyol with good hydrocarbon solubility. Good fire performance with foam swelling. USDA Certified Biobased Product 48%.. Uses: PiP applications. Group: Specialty Chemicals, Polyester Polyol. Alternative Name: EMEROX® 14735. Approvals: USDA Certified Biobased Product 48%.. Pack Sizes: Drums, Totes, Bulk Supply. | |
| Fluorogestone acetate | Fluorogestone Acetate (also known as Flurogestone Acetate, Flugestone Acetate, Fluorogesterone Acetate) was first synthesised by G. D. Searle and Company in 1959. The chemical, which has progestogen activity, was identified as SC-9880. Fluorogestone acetate showed a high potency with short duration of activity and performed physiologically similar to progesterone. FGA was approximately 20 - 25 times more potent than progesterone. Flurogestone acetate was shown to be readily absorbed from impregnated sponges. A 30mg impregnated sponge was effective in blocking ovulation and oestrus, once the sponge was removed impregnated ewes showed visible oestrus, and if inseminated 2 to 4 days after sponge removal showed high conception rates. Synonyms: Flugestone 17-acetate; Flugestone Acetate; 9-Fluoro-11beta,17-dihydroxypregn-4-ene-3,20-dione 17-acetate; NSC 65411; (11beta)17-(Acetyloxy)-9-fluoro-11-hydroxypregn-4-ene-3,20-dione. Grades: 98%. CAS No. 2529-45-5. Molecular formula: C23H31FO5. Mole weight: 406.49. | |
| Graphene oxide, ammonia functionalized | N-doped graphene may be prepared by chemical vapor deposition (CVD), direct synthesis of N-graphene and also by electrical annealing of graphene nanoribbons in NH3 in the presence of NH3.Another technique of preparing N-doped graphene by microbial reduction of graphene oxide was reported. N doping alters the electrical properties of graphene effectively by modifying its band structure. A report also shows that doped graphene can act as excellent support for Pt catalysts and show better performance in Li ion batteries. Uses: Dielectric materials for field effect transistors (fet); non-silicon-based materials for integrated circuits (ic). nitrogen doping (n-doping) can improve electro-conductivity of graphene sheet. Group: 3d printing materials carbon nano materials. | |
| Hydroxypropyl Guar (CAS 39421-75-5) | Hydroxypropyl Guar (HPG) is a modified form of natural guar gum that is commonly used in the food, cosmetics, and pharmaceutical industries as a thickening, stabilizing, and gelling agent. It is produced by chemically modifying the guar gum molecule by attaching hydroxypropyl groups to it. This modification enhances its water solubility and viscosity properties, making it a versatile ingredient in many applications. HPG can be found in various products such as shampoos, body washes, lotions, toothpaste, and various food products such as sauces, gravies, and desserts. Uses: 1. hydroxypropyl guar is commonly used as a thickening agent in personal care and cosmetic products such as shampoos, conditioners, lotions, and soaps. 2. it improves the viscosity and texture of the product, making it easier to apply and enhancing its overall performance. 3. hydroxypropyl guar is also used in the food industry as a stabilizer and thickener, particularly in dairy products like ice cream and yogurt. 4. it can also be used in pharmaceutical products as a binding agent and as a drug delivery system. 5. hydroxypropyl guar is an eco-friendly and biodegradable ingredient that is safe for use in a wide range of consumer products. Group: Rheology modifiers. CAS No. 39421-75-5. Appearance: white, odorless powder that is soluble in water. Catalog: CI-HC-0119. | |
| Lactonic (di-acetylated) Sophorolipids | Lactonic sophorolipid is a natural antimicrobial surfactant for oral hygiene. Lactonic sophorolipid, a potential anticancer agent, induces apoptosis in human HepG2 cells through the caspase-3 pathway. Uses: Widely used in oilfield field, environmental remediation field, agriculture, animal husbandry and aquaculture fields, daily chemicals, cleaning, personal care: it can replace chemical surfactants, with excellent surface performance, safety, biodegradability, strong detergency, low foam type and easy to rinse. Synonyms: 17-L-[(2'-O-β-D-Glucopyranosyl-β-D-glucopyranosyl)oxy]-cis-9-octadecenoic acid 1',4"-lactone 6',6"-diacetate. CAS No. 148409-20-5. Molecular formula: C34H56O14. Mole weight: 688.80. | |
| Methacrylate C6 Phosphoramidite | Methacrylate C6 Phosphoramidite, a complex chemical compound, holds a critical role in biomedical research and diagnostics. It aids in the precise synthesis of DNA and RNA oligonucleotides, boasting both unparalleled efficiency and steadfast stability. With such superior performance, it finds itself on the brink of a new era, with endless opportunities for application in the field. Its potentiality is boundless as it holds promise in the development of drugs tailored to target genetic diseases, including cancer and viral infections. Synonyms: 6-methacrylamido-hexyl-(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramidite. Molecular formula: C19H36N3O3P. Mole weight: 385.48. | |
| Methionine Aminopeptidase from Pyrococcus furiosus, Recombinant | Methionyl aminopeptidase (EC 3.4.11.18, methionine aminopeptidase, peptidase M, L-methionine aminopeptidase, MAP) is an enzyme. This enzyme catalyses the following chemical reaction:Release of N-terminal amino acids, preferentially methionine, from peptides and arylamides. This membrane-bound enzyme is present in both prokaryotes and eukaryotes. X-ray crystallography of the structure of methionine aminopeptidase from pyrococcus furiosus or pfmap was performed at a resolution of 1.75a and showed that the protein consists of a catalytic domain containing two cobalt ions in the active site and a unique insertion domain which is specific to the prokaryotic form of...o the methionyl aminopeptidases from escherichia coli and pyrococcus furiosus. it has also been used in a study to examine the binding of a new class of pseudopeptide analog inhibitors. Group: Enzymes. Synonyms: Methionyl aminopeptidase; EC 3.4.11.18; methionine aminopeptidase; peptidase M; L-methionine aminopeptidase; MAP. Enzyme Commission Number: EC 3.4.11.18. CAS No. 9025-42-7. MAP. Storage: -20°C. Form: Solution containing 0.01% Tween 20, 0.1 mM CoCl2, and 10 mM Tris-HCl, pH 7.5. Source: E. coli. Species: Pyrococcus furiosus. Methionyl aminopeptidase; EC 3.4.11.18; methionine aminopeptidase; peptidase M; L-methionine aminopeptidase; MAP. Cat No: NATE-0442. |  |
| N-[3- (Trimethoxysilyl) Propyl]Ethylenediamine | 3- (2-Aminoethylamino) propyl]trimethoxysilane is a chemical reagent used in organometallic reactions and the process of signal amplification in biomolecular labelling. Uses: It is mainly used to couple organic polymer and inorganic materials in order to improve the mechanical properties, electrical properties, water resistance, aging resistance, etc.this product can improve the performance of the resin laminate of the epoxy, phenolic, melamine, furan, etc. it is also effective to polypropylene, polyethylene, polypropylene of vinegar, silicone, polyamide, polycarbonate and polyvinyl cyanide. Group: Saltself-assembly materials. Alternative Names: N-(3-trimethoxysilylpropyl)ethane-1,2-diamine; 3- (2-Aminoethylamino) propyltrimethoxysilane; N1-(3-(Trimethoxysilyl)propyl)ethane-1,2-diamine; 1,2-Ethanediamine, N-[3-(trimethoxysilyl)propyl]-; N-(2-Aminoethyl)-3-aminopropyltrimethoxysilane. CAS No. 1760-24-3. Pack Sizes: N-[3- (Trimethoxysilyl) propyl]ethylenediamin (A-1120, KBM-603, OFS-6020, DAMO) is packed in 25KG/200KG drum, IBC tank or ISO tank. It is sealed and stored in cool and well ventilated place away from fire and water. Product ID: N'-(3-trimethoxysilylpropyl)ethane-1,2-diamine. Molecular formula: 222.36. Mole weight: C8H22N2O3Si. CO[Si](CCCNCCN)(OC)OC. InChI=1S/C8H22N2O3Si/c1-11-14(12-2, 13-3)8-4-6-10-7-5-9/h10H, 4-9H2, 1-3H3. PHQOGHDTIVQXHL-UHFFFAOYSA-N. | |
| N-[3- (Trimethoxysilyl) Propyl]Ethylenediamine | 3- (2-Aminoethylamino) propyl]trimethoxysilane is a chemical reagent used in organometallic reactions and the process of signal amplification in biomolecular labelling. Uses: It is mainly used to couple organic polymer and inorganic materials in order to improve the mechanical properties, electrical properties, water resistance, aging resistance, etc.this product can improve the performance of the resin laminate of the epoxy, phenolic, melamine, furan, etc. it is also effective to polypropylene, polyethylene, polypropylene of vinegar, silicone, polyamide, polycarbonate and polyvinyl cyanide. Group: Biomaterials. Alternative Names: N- (3-trimethoxysilylpropyl) ethane-1, 2-diamine; 3- (2-Aminoethylamino) propyltrimethoxysilane; N1- (3- (Trimethoxysilyl) propyl) ethane-1, 2-diamine; 1, 2-Ethanediamine, N-[3-(trimethoxysilyl)propyl]-;N-(2-Aminoethyl)-3-aminopropyltrimethoxysilane. CAS No. 1760-24-3. Molecular formula: C8H22N2O3Si. Mole weight: 222.36. Appearance: Colorless transparent liquid. IUPACName: N'-(3-trimethoxysilylpropyl)ethane-1,2-diamine. Canonical SMILES: CO[Si](CCCNCCN)(OC)OC. Density: 1.03 g/mL. ECNumber: 217-164-6. Catalog: ACM1760243. | |
| Native Crotalus adamanteus L-Amino Acid Oxidase | In enzymology, an L-amino acid oxidase (LAAO) (EC 1.4.3.2) is an enzyme that catalyzes the chemical reaction:an L-amino acid + H2O + O2<-> a 2-oxo acid + NH3 + H2O2. The enzyme was first described in 1944 by A. Zeller and A. Maritz. Not only are LAAOs quite variable in terms of molecular mass, they also vary widely regarding stability. In a similar vein, this enzyme performs in a myriad of biological activities including apoptosis-induction, edema-induction, hemorrhaging, and inhibition or induction of platelet aggregation. Applications: L-amino acid oxidase (laao) is used to convert l-amino acids to their corresponding α-keto acids. one unit will oxidatively de...w-injection pr ocedure with chemiluminescence detection for on-site determination of l-alanine. Group: Enzymes. Synonyms: L-amino acid oxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acid oxidase; L-amino-acid:oxygen oxidoreductase (deaminating). Enzyme Commission Number: EC 1.4.3.2. CAS No. 9000-89-9. LAAO. Activity: Type I, > 0.3 unit/mg solid; Type II, > 3.0 units/mg protein (biuret). Storage: Type I, -20°C; Type II, 2-8°C. Form: Type I, dried venom; Type II, aqueous suspension. Source: Crotalus adamanteus. L-amino acid oxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acid oxidase; L-amino-acid:oxygen oxidoreductase (deaminating). Cat No: NATE-0366. | |
| Native Crotalus atrox L-Amino Acid Oxidase | In enzymology, an L-amino acid oxidase (LAAO) (EC 1.4.3.2) is an enzyme that catalyzes the chemical reaction:an L-amino acid + H2O + O2<-> a 2-oxo acid + NH3 + H2O2. The enzyme was first described in 1944 by A. Zeller and A. Maritz. Not only are LAAOs quite variable in terms of molecular mass, they also vary widely regarding stability. In a similar vein, this enzyme performs in a myriad of biological activities including apoptosis-induction, edema-induction, hemorrhaging, and inhibition or induction of platelet aggregation. Applications: L-amino acid oxidase is used to convert l-amino acids to their corresponding α-keto acids. this product is from crotalus atrox. one unit will oxidatively deaminate 1.0 μmole of l-phenylalanine per min at ph 6.5 at 37°c. l-amino acid oxidase, from creative enzymes, has been used in leucine aminopeptidase (lap) activity assays. Group: Enzymes. Synonyms: L-amino acid oxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acid oxidase; L-amino-acid:oxygen oxido. Enzyme Commission Number: EC 1.4.3.2. CAS No. 9000-89-9. LAAO. Activity: > 0.10 unit/mg solid. Storage: -20°C. Form: dried venom. Source: Crotalus atrox (Western Diamondback Rattlesnake). L-amino acid oxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acid oxidase; L-amino-acid:oxygen oxidoreductase (deaminating). Cat No: NATE-0367. | |
| Native Crotalus durissus venom L-Amino Acid Oxidase | In enzymology, an L-amino acid oxidase (LAAO) (EC 1.4.3.2) is an enzyme that catalyzes the chemical reaction:an L-amino acid + H2O + O2<-> a 2-oxo acid + NH3 + H2O2. The enzyme was first described in 1944 by A. Zeller and A. Maritz. Not only are LAAOs quite variable in terms of molecular mass, they also vary widely regarding stability. In a similar vein, this enzyme performs in a myriad of biological activities including apoptosis-induction, edema-induction, hemorrhaging, and inhibition or induction of platelet aggregation. Applications: L-amino acid oxidase (laao) is used to convert l-amino acids to their corresponding α-keto acids. this product is from crotalus durissus venom. l-amino acid oxidase, from creative enzymes, has been used in leucine aminopeptidase (lap) activity assays. Group: Enzymes. Synonyms: L-amino acid oxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acid oxidase; L-amino-acid:ox. Enzyme Commission Number: EC 1.4.3.2. CAS No. 9000-89-9. LAAO. Activity: 3-8 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 3.2 M (NH4)2SO4 pH approx. 6. Source: Crotalus durissus venom. L-amino acid oxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acid oxidase; L-amino-acid:oxygen oxidoreductase (deaminating). Pack: Package size based on protein content. Cat No: NATE-0368. | |
| PET engineering plastics | PBT resin demonstrates strong mechanical properties while maintaining dimensional stability. Due to excellent electrical resistance, PBT is commonly used in electrical applications where minimal energy absorption improves performance, as well as in automotive components where heat and chemical resistance is needed. Uses: Mainly used in various energy-saving lamps: bulbs, candle lights, spotlights, downlights and other products as heat dissipation components. Group: Polybutylene terephthalate (pbt). | |
| Platinum paste, screen printable | Silvery, whitish-gray, malleable, ductile metal. Mp: 1772°C; bp: 2187°C. Density: 21.45 g cm-3 at room conditions (very dense). Also shipped as a finely divided powder (platinum black), as a sponge, and as particles deposited on a supporting material such as alumina. Has strong catalytic activity in these forms; finely divided platinum can be dangerous to handle in the vicinity of other chemicals on this account. Used platinum catalysts are particularly dangerous and can be explosive.;OtherSolid;Solid;BLACK POWDER.;Silvery, whitish-gray, malleable, ductile metal.;Silvery, whitish-gray, malleable, ductile metal. Uses: Pt1 platinum paste can be used in applications that require a highly transparent layer with high electrocatalytic activity.pt1 platinum paste is oil-based and formulated to be applied using a screen printer; providing films with excellent uniformity; performance and reproducibility; and can be used for dssc polot production. after drying; this paste must be fired at or above 420°c. this results in. Group: 3d printing materials organic solar cell (opv) materials printed electronic materials. Alternative Names: Dyesol(R) PT1 platinum paste,Pt paste,conductive paste. Pack Sizes: 20 g in glass bottle. Product ID: platinum. Molecular formula: 195.08g/mol. Mole weight: Pt. [Pt]. 1S/Pt. BASFCYQUMIYNBI-UHFFFAOYSA-N. | |
| Poly(3-octylthiophene-2,5-diyl) | Greater than 98.5% head-to-tail regiospecific conformation. Poly(3-octylthiophene-2,5-diyl) (P3OT) is an alkylthiophene based conductive polymer with high electroluminescence, which is soluble in most of the organic solvents. It can be prepared by the electrochemical polymerization of 3-octylthiophene (3OT). It is hydrophobic and can be used as a transducer for ion selective electrodes. Uses: P3ot forms a nanocomposite with carbon nanotubes (cnts) for devising a high performance semiconducting material. it can also be used as a π-conjugating polymer for the fabrication of organic electronic based devices which include polymeric diodes, solar cells and photovoltaic modules. rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, m. Group: Bioelectronic materials organic field effect transistor (ofet) materials organic light-emitting diode (oled) materials organic solar cell (opv) materials. Alternative Names: P3OT. CAS No. 104934-51-2. Pack Sizes: 1 g in glass bottle,Packaged in glass bottles. Product ID: 3-octylthiophene. Molecular formula: average Mn ~34,000. Mole weight: (C12H18S)n. CCCCCCCCC1=CSC=C1. InChI=1S / C12H20S / c1-2-3-4-5-6-7-8-12-9-10-13-11-12 / h9-11H, 2-8H2, 1H3. WQYWXQCOYRZFAV-UHFFFAOYSA-N. | |
| Poly(3-octylthiophene-2,5-diyl) | Greater than 98.5% head-to-tail regiospecific conformation. Poly(3-octylthiophene-2,5-diyl) (P3OT) is an alkylthiophene based conductive polymer with high electroluminescence, which is soluble in most of the organic solvents. It can be prepared by the electrochemical polymerization of 3-octylthiophene (3OT). It is hydrophobic and can be used as a transducer for ion selective electrodes. Uses: P3ot forms a nanocomposite with carbon nanotubes (cnts) for devising a high performance semiconducting material. it can also be used as a π-conjugating polymer for the fabrication of organic electronic based devices which include polymeric diodes, solar cells and photovoltaic modules. rechargeable battery electrodes, electrochromic devices, chemical and optical sensors, light-emitting diodes, m. Group: Polymer/macromolecule. Alternative Names: P3OT. CAS No. 104934-51-2. Molecular formula: (C12H18S)n. Mole weight: average Mn ~34,000. Appearance: black. IUPACName: 3-octylthiophene. Canonical SMILES: CCCCCCCCC1=CSC=C1. Catalog: ACM104934512-8. | |
| Poly(ethylene-co-acrylic acid), acrylic acid 15 wt. % | Forms reversible ionic clusters (crosslinks). Promotes adhesion to various substrates, tougher, more chemically resistant and more transparent than parent acid copolymer. Uses: Processing and performance additive. promotes crystallization of pet. assists dispersion of additives in plastics. Group: Acrylics. CAS No. 9010-77-9. Molecular formula: (CH2CH2)x[CH2CH(CO2H)]y. Canonical SMILES: C=C.OC(=O)C=C. Density: 0.93 g/mL at 25 °C. Catalog: ACM9010779. | |
| Polyethylene Terephthalate | PET is a general-purpose thermoplastic polymer that belongs to the polyester family of polymers. Known for their excellent combination of properties such as mechanical, thermal, chemical resistance as well as dimensional stability, polyester resins are suitable for extruded applications that require clarity, toughness and consistent processing performance. PET can be alloyed and compounded with engineering resins. Polyester resins are low cost, withstand temperatures up to 80?C, offer good wetting to glass fibers, have a relatively low shrinkage of 4% ? 8% during curing, and provide a linear expansion ranging from 100 - 200 x 10-6 K-1. Uses: Used in electrical parts including relay bases and lamp sockets, pump housings, gears, sprockets, chair arms, casters and furniture components. Group: Polyethylene terephthalate (pet). Alternative Names: PET. CAS No. 25038-59-9. Product ID: poly(ethylene terephthalate). Molecular formula: 228.2g/mol. Mole weight: C10H12O6. OCCO.OC(=O)c1ccc(cc1)C(O)=O. InChI=1S/C8H6O4. C2H6O2/c9-7 (10)5-1-2-6 (4-3-5)8 (11)12; 3-1-2-4/h1-4H, (H, 9, 10) (H, 11, 12); 3-4H, 1-2H2. FYIBGDKNYYMMAG-UHFFFAOYSA-N. | |
| Polyethylene Terephthalate, (polyester, PET, PETP), fabric, weight.m-2-92g, thickness 0.13 mm | PET is a general-purpose thermoplastic polymer that belongs to the polyester family of polymers. Known for their excellent combination of properties such as mechanical, thermal, chemical resistance as well as dimensional stability, polyester resins are suitable for extruded applications that require clarity, toughness and consistent processing performance. PET can be alloyed and compounded with engineering resins. Polyester resins are low cost, withstand temperatures up to 80?C, offer good wetting to glass fibers, have a relatively low shrinkage of 4% ? 8% during curing, and provide a linear expansion ranging from 100 - 200 x 10-6 K-1. Uses: Food and beverage bottles and containers | flexible food packaging | thermal insulation | clothing | biaxially oriented pet film | tape (magnetic, pressure-sensitive adhesive) | 3d printing filament | 3d printing plastic petg | alloy with engineering resins | disposable packaging trays | blister packs | thin film solar cells | waterproof barrier in undersea cables. Group: Polyethylene terephthalate (pet). | |
| Polyphenylene sulfide (PPS) | Polyphenylene sulfide (PPS) is a high-performance engineering thermoplastic with high temperature. It has a semi-crystalline structure with a unique combination of properties. They range from dimensional and thermal stability to high temperature and chemical resistance. (PPS), film, thickness 0.1 mm, size 100 × 100 mm, natural. Uses: Thanks to its exceptional dimensional stability, low density, corrosion and hydrolysis resistance, pps can be used to manufacture heating and air conditioning components, fry pan handles, hair dryer grills, steam iron valves, toaster and dryer switches, microwave oven turntables etc. in electric appliances. Group: Polyphenylene sulfide (pps). | |
| Potassium Alginate | Potassium alginate occurs as a white to yellowish, fibrous or granular powder; it is almost odorless and tasteless. Synonyms: Alginic acid, potassium salt; E402; Improved Kelmar; potassium polymannuronate. CAS No. 9005-36-1. Product ID: PE-0563. Molecular formula: (C6H7O6K)n. Category: Emulsifying Agents; Stabilizing Agents; Suspending Agents; Thickening Agents. Product Keywords: Stabilizers; Emulsifier Excipients; Suspending Agents; ; PE-0563; Potassium Alginate; Emulsifying Agents; Stabilizing Agents; Suspending Agents; Thickening Agents; (C6H7O6K)n; 9005-36-1. UNII: 44ZPJ5W2J1. Chemical Name: Potassium alginate. Grade: Pharmceutical Excipients. Stability and Storage Conditions: In the solid state, potassium alginate is a stable material that is not prone to microbial spoilage. Over time, a slow reduction in the degree of polymerization can occur, which may be reflected in a reduction in the viscosity of solutions. As both temperature and moisture can impair the performance of potassium alginate, storage below 25°C is recommended. Potassium alginate solutions are stable at pH 4-10; long-term storage outside this range can result in depolymerization of the polymer through hydrolysis. Gelation or precipitation of the alginate can occur at pH values less than 4. Liquid or semisolid alginate formulations should be preserved: suitable preservatives are sodium benzoate, potassium sorbate, or parabens. Potassium algin |  |
| Pyrrolidone Carboxylate | Sodium L-pyroglutamate, also known as sodium pyrrolidone carboxylic acid (NaPCA), is a naturally occurring amino acid derived from glutamic acid. It exists as a white crystalline powder and is readily soluble in water and alcohol. NaPCA finds wide application in various industries. In the food industry, it is utilized as an emulsifier and stabilizer, while the cosmetic industry employs it as a moisturizer and humectant. Additionally, NaPCA has been incorporated into nutraceuticals, and medical products. Synonyms: Sodium PCA;sodium 5-oxo-L-prolinate;Sodium Pyrrolidone Carboxylate;Na-PCA;L-PCA-NA;PCA-Na NL-50;(S)-sodium PCA;sodium pidolate;L-PCA-Na=SodiumPCA;dium L-pyroglutamate. CAS No. 28874-51-3. Product ID: CDC10-0720. Molecular formula: C5H6NNaO3. Mole weight: 151.1. Product Keywords: Moisturizers; CDC10-0720; Pyrrolidone Carboxylate; 28874-51-3; Sodium PCA;sodium 5-oxo-L-prolinate;Sodium Pyrrolidone Carboxylate;Na-PCA;L-PCA-NA;PCA-Na NL-50;(S)-sodium PCA;sodium pidolate;L-PCA-Na=SodiumPCA;dium L-pyroglutamate. Chemical Name: Sodium L-pyroglutamate. Grade: Cosmetic grade. Applications: sodium PCA (Ajidew NaPCA, Nalidone) is a high-performance humectant given its moisture-binding ability. Sodium PCA is a component of the skins natural moisturizing factor. For cosmetic use, it is derived from amino acids. It is considered a noncomedogenic, non-allergenic raw material recommended for dry, delicate, and sens | |
| Sodium Hypochlorite (Bleach) | Sodium Hypochlorite, also known as bleach is used to effectively clean and sanitize equipment, floors, and walls in facilities where food is prepared, and to perform many other cleaning needs, as well as uses like cleaning hard surfaces. Contact Level 7 Chemical today for your sodium hypochlorite requirements. Uses: Sanitation, Cleaning, Stain removal. Alternative Names: Bleach, Sodium Hypochlorite CAS # 7681-52-9. Grades: NSF, Food, 12.5 % 15 %. CAS No. 7681-52-9. Pack Sizes: 55 gallon Drums, 220 gallon Totes. |  USA |
| Sodium nitrite | Chemical formula is NaNO2, in which N has a valency is + III.It is colorless or yellow crystal, the relative density is 2.168 (0?), the melting point is 271?, and it is decomposed when 320?. It is soluble in water, and aqueous solution is alkaline because of nitrate hydrolysis. Sodium nitrite has the characteristics of reduction and oxidation and is mainly oxidation. In acidic solution, the main performance is oxidation. In alkaline solution or in case of strong oxidizing agent, its performance is reduction. With sulfur, phosphorus, organic matter and other friction or impact can cause combustion or explosion. Sodium nitrite can be placed in the air with the oxygen reaction, and gradually produce sodium nitrate: NaNO2+1/2O2=NaNO3. Uses: When using strong acidic sodium nitrite, it can be nitrited to nitric acid. nitrite is very unstable, easily decomposed into nitrogen dioxide, nitric oxide and water. Synonyms: NITRITE CONCENTRATE ION STANDARD. CAS No. 7632-00-0. Molecular formula: NaNO2. | |
| Sodium phosphate tribasic dodecahydrate | Sodium phosphate tribasic dodecahydrate. Synonyms: TSP, Trisodium phosphate (tert) dodecahydrate, Trisodium phosphate dodecahydrate. CAS No. 10101-89-0. Product ID: CDC10-0125. Molecular formula: Na3PO4·12H2O. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Sodium phosphate tribasic dodecahydrate; CDC10-0125; 10101-89-0; Na3PO4·12H2O; Trisodium phosphate dodecahydrate; 231-509-8; MFCD00149198; 10101-89-0. Purity: ≥98%. EC Number: 231-509-8. Physical State: Crystalline. Solubility: Alcohol: insoluble. Quality Level: 200. Storage: Store at 5°C to 30°C. Application: Sodium phosphate tribasic dodecahydrate was used to prepare buffer solution used in the analysis of pyronaridine in human whole blood and plasma by using high-performance liquid chromatography. Melting Point: 75 °C. Density: 1.62 g/mL at 25 °C. | |
| Sodium pyrophosphate tetrabasic | Sodium pyrophosphate tetrabasic. Synonyms: Sodium diphosphate tetrabasic, Tetrasodium pyrophosphate. CAS No. 7722-88-5. Pack Sizes: 500 g in poly bottle. Product ID: CDC10-0127. Molecular formula: Na4P2O7. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Sodium pyrophosphate tetrabasic; CDC10-0127; 7722-88-5; Na4P2O7; Sodium diphosphate tetrabasic, Tetrasodium pyrophosphate; 231-767-1; MFCD00003513; 7722-88-5. Purity: ≥95%. Color: White. EC Number: 231-767-1. Physical State: Powder. Quality Level: 200. Storage: Inert atmosphere,Room Temperature. Application: Na4P2O7 can be used as an inorganic additive to improve the stability and electrochemical performance of redox flow batteries. Boiling Point: 93.8°C. Melting Point: 80°C. Density: 2.53 g/mL at 25 °C (lit.). Product Description: Sodium pyrophosphate tetrabasic (Na4P2O7) is a non-toxic and biocompatible compound used as an electroactive media for exfoliation of the surface coating. It is also be used as an additive in the food industry. | |
| Uridine, 3'-?deoxy-?3'-?[[ (4-?methoxyphenyl) ?diphenylmethyl]?amino]?-?2'-?O-?methyl-?, 5'-?[2-?cyanoethyl bis(1-?methylethyl)?phosphoramidite] (9CI) | Uridine, 3'-deoxy-3'-[[(4-methoxyphenyl)diphenylmethyl]amino]-2'-O-methyl-, 5'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite] (9CI) is an essential chemical compound utilized in nucleoside analogue development to combat viral diseases and cancer. Interestingly, this natural building block is employed to synthesize oligonucleotides that can specifically target genes or viral RNA. Uridine derivatives perform a crucial role in improving the pharmacokinetic and pharmacological properties of nucleoside analogs, thereby enhancing their therapeutic efficacy to combat lethal illnesses. Synonyms: 2-cyanoethyl ( ( (2S, 3R, 4R, 5R) -5- (2, 4-dioxo-3, 4-dihydropyrimidin-1 (2H) -yl) -4-methoxy-3- ( ( (4-methoxyphenyl) diphenylmethyl) amino) tetrahydrofuran-2-yl) methyl) diisopropylphosphoramidite. CAS No. 329773-19-5. Molecular formula: C39H48N5O7P. Mole weight: 729.8. | |
| VPC-70063 | VPC-70063 is a Myc-Max inhibitor. VPC-70067 is a close analog of the previously identified Myc inhibitor 10058-F4. VPC-70063, of a chemically different scaffold, was the best performer in a panel of in vitro assays, and the forerunner for future hit-to-lead optimization efforts. Group: Inhibitors. Alternative Names: VPC-70063; VPC 70063; VPC70063. CAS No. 13571-44-3. Molecular formula: C16H12F6N2S. Mole weight: 378.34. Appearance: Solid powder. Purity: >98%. IUPACName: N-[3, 5-Bis (trifluoromethyl)phenyl]-N'- (phenylmethyl)thiourea. Canonical SMILES: S=C (NCC1=CC=CC=C1)NC2=CC (C (F) (F)F)=CC (C (F) (F)F)=C2. Catalog: ACM13571443. | |
