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This formulation is Doxorubicin Liposome (PEGylated) with the cyanur group. Proteins can be covalently coupled to the liposome via amine-reactive cyanur-groups, either directly to the vesicle surface using cyanuric chloride-activated DSPE (cyanur-DSPE) or to the distal ends of PEG-spacers using activated cyanur-PEG-PE (ammonium salt). Cyanuric chloride at the PEG terminus functions to link peptides, antibodies and other amine-containing biomolecules or nanoparticles via a nucleophilic substitution reaction under basic conditions. Antibodies or other proteins can be conjugated without any previous derivatization. Group: Drug-loaded liposome. Categories: liposomes, niosomes, ethosomes, and transfersomes.
Cyanuric acid
1,3,5-Triazine-2,4,6-triol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 108-80-5. Pack Sizes: 100 g. Product ID: HY-W010407.
Cyanuric acid
Cyanuric acid. Group: Biochemicals. Alternative Names: 1,3,5-Triazine-2,4,6-triol; 1,3,5-Triazine-2,4,6-trione; 2,4,6-Trihydroxy-1,3,5-triazine. Grades: Highly Purified. CAS No. 108-80-5. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C3H3N3O3. US Biological Life Sciences.
Diagnostic determination of Melamine and related compounds in kidney tissue. Group: Biochemicals. Alternative Names: 1,3,5-Triazine-2,4,6-triol; 1,3,5-Triazine-2,4,6-trione; 2,4,6-Trihydroxy-1,3,5-triazine; 2,4,6-Trihydroxy-s-triazine. Grades: Highly Purified. CAS No. 108-80-5. Pack Sizes: 1g. US Biological Life Sciences.
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Cyanuric Acid 108-80-5
Cyanuric Acid 108-80-6. SUPPLIERS TO BUSINESS CUSTOMERS ONLY.
North America & APAC
Cyanuric acid-13C3
Cyanuric acid- 13 C 3 is the 13 C labeled Cyanuric acid[1]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 201996-37-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-W010407S.
Cyanuric Acid-13C3
Useful for diagnostic determination of Melamine and related compounds in kidney tissue. Group: Biochemicals. Alternative Names: 1,3,5-Triazine-2,4,6-triol-13C3; 1,3,5-Triazine-2,4,6-trione-13C3; 2,4,6-Trihydroxy-1,3,5-triazine-13C3; 2,4,6-Trihydroxy-s-triazine-13C3; NSC 6284-13C3; Pseudocyanuric Acid-13C3; Tricyanic Acid-13C3. Grades: Highly Purified. CAS No. 201996-37-4. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
cyanuric acid amidohydrolase
Along with EC 3.5.1.54 (allophanate hydrolase) and EC 3.5.1.84 (biuret amidohydrolase), this enzyme forms part of the cyanuric-acid metabolism pathway, which degrades s-triazide herbicides, such as atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine], in bacteria. This is a key enzyme in the pathway, catalysing the ring cleavage of cyanuric acid. The enzyme is specific for cyanuric acid as substrate as neither the structurally related compounds ammeline (2,4-diamino-6-hydroxy-s-triazine) and ammelide (2-amino-4,6-dihydroxy-s-triazine) nor a number of pyrimidine compounds, such as uracil and cytosine, can act as substrates. Group: Enzymes. Synonyms: AtzD. Enzyme Commission Number: EC 3.5.2.15. CAS No. 132965-78-7. 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-4498; cyanuric acid amidohydrolase; EC 3.5.2.15; 132965-78-7; AtzD. Cat No: EXWM-4498.
Cyanuric Chloride is extensively used in the preparation of the triazine-class pesticides and herbicides. Cyanuric chloride is also used as a precursor to dyes and crosslinking agents due to the reactive chlorine atoms towards nucleophilic substitution reactions. Cyanuric chloride derivatives possess a large spectrum of activities as antibacterial and anticancer agents. Group: Biochemicals. Alternative Names: 1,3,5-Trichloro-2,4,6-triazine; 1,3,5-Trichlorotriazine; 2,4,6-Trichloro-1,3,5-triazine; 2,4,6-Trichloro-s-triazine; 2,4,6-Trichloro-sym-triazine; 2,4,6-Trichlorotriazine; Cyanur Chloride; Cyanuric Chloride; Cyanuric Trichloride; Isocyanuric Trichloride; NSC 3512; Solgel W 08; Trichloro-s-triazine; Trichlorocyanidine; Zorugeru W 08; s-Triazine Trichloride; sym-Trichlorotriazine. Grades: Highly Purified. CAS No. 108-77-0. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Cyanuric Chloride-13C3
A coupling agent used in the immobilization of microorganisms to cellulose and activation of polysaccharides. Group: Biochemicals. Alternative Names: 1,3,5-Trichloro-2,4,6-triazine-13C3; 1,3,5-Trichlorotriazine-13C3; 2,4,6-Trichloro-1,3,5-triazine-13C3; 2,4,6-Trichloro-s-triazine-13C3; 2,4,6-Trichloro-sym-triazine-13C3; 2,4,6-Trichlorotriazine-13C3; Cyanur Chloride-13C3; Cyanuric Chloride-13C3; Cyanuric Trichloride-13C3; Isocyanuric Trichloride-13C3; NSC 3512-13C3; Solgel W 08-13C3; Trichloro-s-triazine-13C3; Trichlorocyanidine-13C3; Zorugeru W 08-13C3; s-Triazine Trichloride-13C3; sym-Trichlorotriazine-13C3. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences.
Worldwide
Cyanurotriamide
Melamine appears as colorless to white monoclinic crystals or prisms or white powder. Sublimes when gently heated. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; WetSolid;Solid;COLOURLESS-TO-WHITE CRYSTALS. Group: Polymers. Product ID: 1,3,5-triazine-2,4,6-triamine. Molecular formula: 126.12g/mol. Mole weight: C3H6N6;C3N3(NH2)3;C3H6N6. C1(=NC(=NC(=N1)N)N)N. InChI=1S/C3H6N6/c4-1-7-2 (5)9-3 (6)8-1/h (H6, 4, 5, 6, 7, 8, 9). JDSHMPZPIAZGSV-UHFFFAOYSA-N.
1,3,5-Tris(2-hydroxyethyl)cyanuric acid. Uses: Designed for use in research and industrial production. Product Category: THEIC. CAS No. 839-90-7. Product ID: ACM839907. Alfa Chemistry ISO 9001:2015 Certified.
Tris(3,5-di-tert-butyl-4-hydroxybenzyl) Isocyanurate is used an as antioxidant-stabilizer in polyolefin films intended for packaging nonfatty food as well as an antioxidant in propylene copolymers. Group: Biochemicals. Alternative Names: 1,3,5-Tri(3,5-di-tert-butyl-4-hydroxybenzyl) Isocyanurate; 1,3,5-Tris(3,5-di-tert-butyl-4-hydroxybenzyl) Isocyanurate; 1,3,5-Tris(3,5-di-tert-butyl-4-hydroxybenzyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione; 1,3,5-Tris(3,5-di-tert-butyl-4-hydroxybenzyl)-s-triazin-2,4,6(1H,3H,5H)-trione; 1,3,5-Tris(3,5-di-tert-butyl-4-hydroxybenzyl)-s-triazine-2,4,6(1H,3H,5H)-trione; 1,3,5-Tris(3,5-di-tert-butyl-4-hydroxybenzyl)-s-triazinetrione; 1,3,5-Tris(3',5'-di-tert-butyl-4'-hydroxybenzyl)-5-triazine-2,4,6(1H,3H,5H)-trione; 1,3,5-Tris(4-hydroxy-3,5-di-tert-butylbenzyl)cyanuric acid; 1, 3, 5-tris(3, 5-di-tert-butyl-4-hydroxybenzyl)[1, 3, 5]triazin-2, 4, 6-trione; ADK Stab AO 18; ADK Stab AO 20; AO 106; AO 18; AO 2; AO 20; AT 3114; AgeRite GT; Alvinox FB; Anox 3114; Anox IC 14; Antioxidant 3114; Cyanox 1741; E 043; Ethanox 314; G 3114; Good-rite 3114; Hostanox M 014; IR 3114; Irganox 3114; Keminox 314; Mark AO 18; Mark AO 20; Mixxim AO 20; Thanox 3114; Vanox GT; Vixid; Yoshinox 314. Grades: Highly Purified. CAS No. 27676-62-6. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
2,?4,?6-?Trifluoro-s-triazine
2,?4,?6-?Trifluoro-s-triazine is an aromatic intermediate compound useful for the preparation of substituted melamine, ammelides, and ammelines. Group: Biochemicals. Alternative Names: 1,3,5-Trifluoro-2,4,6-triazine; 2,4,6-Trifluoro-1,3,5-triazine; 2,4,6-Trifluoro-?s-triazine; 2,4,6-Trifluoro-sym-triazine; 2,4,6-Trifluorotriazine; Cyanuric Trifluoride; NSC 168386; Trifluoro-1,3,5-triazine; Trifluoro-s-triazine. Grades: Highly Purified. CAS No. 675-14-9. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
2,4,6-Trimercapto-s-Triazine
2,4,6-Trimercapto-s-Triazine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Trithiocyanuric acid, Thiocyanuric acid, 638-16-4, Trismercaptotriazine, 1,3,5-Triazine-2,4,6-trithiol, Trimercaptocyanuric acid, Cyanuric acid, trithio-, USAF TH-3, 1,3,5-Triazine-2,4,6(1H,3H,5H)-trithione, 2,4,6-Trimercapto-s-triazine, 2,4,6-Triazinetrithiol, 1,3,5-Trimercaptotriazine, EINECS 211-322-8, S-TRIAZINE-2,4,6-TRITHIOL, NSC 62071, NSC 65480, SBB057054, 1,3,5-triazinane-2,4,6-trithione, 2,4,6-Trimercapto-1,3,5-triazine, 1,3,5-Triazine-2,4,6-trimercaptan. Product Category: Heterocyclic Organic Compound. CAS No. 2060-82-4. Molecular formula: C3H3N3S3. Mole weight: 177.271020 [g/mol]. Purity: 0.96. IUPACName: 1,3,5-triazinane-2,4,6-trithione. Canonical SMILES: C1(=S)NC(=S)NC(=S)N1. ECNumber: 211-322-8. Product ID: ACM2060824. Alfa Chemistry ISO 9001:2015 Certified.
2,4,6-Tris(2,4,6-tribomophenoxy)-1,3,5-triazine
2,4,6-Tris(2,4,6-tribomophenoxy)-1,3,5-triazine. Group: Biochemicals. Alternative Names: Tris(tribromophenyl) Cyanurate; FR-245; 2,4,6-Tris(2,4,6-tribromophenoxy)-s-Triazine; FR 235; FR 245; FR 368; GX 6145; Pyroguard SR 245; SR 245. Grades: Highly Purified. CAS No. 25713-60-4. Pack Sizes: 10mg. Molecular Formula: C21H6Br9N3O3, Molecular Weight: 1067.43. US Biological Life Sciences.
Along with EC 3.5.2.15 (cyanuric acid amidohydrolase) and EC 3.5.1.84 (biuret amidohydrolase), this enzyme forms part of thecyanuric-acid metabolism pathway, which degrades s-triazide herbicides, such as atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine], in bacteria. The yeast enzyme (but not that from green algae) also catalyses the reaction of EC 6.3.4.6, urea carboxylase, thus bringing about the hydrolysis of urea to CO2 and NH3 in the presence of ATP and bicarbonate. The enzyme from Pseudomonas sp. strain ADP has a narrow substrate specificity, being unable to use the structurally analogous compounds urea, hydroxyurea or methylcarbamate as substrate. Group: Enzymes. Synonyms: allophanate lyase; AtzF; TrzF. Enzyme Commission Number: EC 3.5.1.54. CAS No. 9076-72-6. 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-4443; allophanate hydrolase; EC 3.5.1.54; 9076-72-6; allophanate lyase; AtzF; TrzF. Cat No: EXWM-4443.
biuret amidohydrolase
Along with EC 3.5.2.15 (cyanuric acid amidohydrolase) and EC 3.5.1.54 (allophanate hydrolase), this enzyme forms part of thecyanuric-acid metabolism pathway, which degrades s-triazide herbicides, such as atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine], in bacteria.Urea-1-carboxylate rather than urea (as was thought previously) is the 2-nitrogen intermediate in cyanuric-acid metabolism in bacteria. The product, urea-1-carboxylate,can spontaneously decarboxylate under acidic conditions to form urea but, under physiological conditions, it can be converted into CO2 and ammonia by the action of EC 3.5.1.54. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.84. CAS No. 95567-88-7. 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-4475; biuret amidohydrolase; EC 3.5.1.84; 95567-88-7. Cat No: EXWM-4475.