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| Product | Description | |
|---|---|---|
| Tolcapone ( (3, 4-Dihydroxy-5-nitro-phenyl) (4-methylphenyl) methanone, Ro-40-7592, Tasmar) | Orally active inhibitor of central and peripheral catechol-O-methyltransferase (COMT). Antiparkinsonian. Group: Biochemicals. Alternative Names: (3, 4-Dihydroxy-5-nitro-phenyl) (4-methylphenyl) methanone; Ro-40-7592; Tasmar. Grades: Highly Purified. CAS No. 134308-13-7. Pack Sizes: 100mg. US Biological Life Sciences. |  Worldwide |
| Tolcapone-d4 | Orally active inhibitor of central and peripheral catechol-O-methyltransferase (COMT). Antiparkinsonian. Group: Biochemicals. Alternative Names: (3,4-Dihydroxy-5-nitrophenyl)(4-methylphenyl-d4)methanone; Ro-40-7592-d4; Tasmar-d4. Grades: Highly Purified. CAS No. 1246816-93-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tolcapone-[d4] | Tolcapone-[d4] is the labelled analogue of Tolcapone. Tolcapone is a nitrocatechol-type inhibitor of the enzyme catechol-O-methyltransferase. It can be used to treat Parkinson's disease. Synonyms: Tolcapone D4; (3,4-Dihydroxy-5-nitrophenyl)(4-methylphenyl-d4)methanone. Grade: 95% by HPLC; 98% atom D. CAS No. 1246816-93-2. Molecular formula: C14H7D4NO5. Mole weight: 277.27. |  |
| Tolcapone-[d7] | An isotope labelled form of Tolcapone. Tolcapone is a nitrocatechol-type inhibitor of the enzyme catechol-O-methyltransferase. It can be used to treat Parkinson's disease. Synonyms: Tolcapone-d7; 5-[4-(D3)methyl(D4)benzoyl]-3-nitrobenzene-1,2-diol. Grade: 95% by HPLC; 98% atom D. CAS No. 2749285-04-7. Molecular formula: C14H4D7NO5. Mole weight: 280.28. | |
| Tolcapone Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Tolcapone Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Tolcide 2230 | Antimicrobial agent used as a substitute for chlorophenols in industrial applications. Group: Biochemicals. Alternative Names: Thiocyanic Acid (2-Benzothiazolylthio) methyl Ester; 2- (Thiocyanato methyl thio) benzo [d] thiazole. Grades: Highly Purified. CAS No. 21564-17-0. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tolclofos-methyl | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Tolclofos-methyl | Tolclofos-methyl is a broad-spectrum aromatic hydrocarbon fungicide that is used as a see treatment for protection against soil-borne and seed borne fungal pathogens that caused seed decay and seedling blights. Uses: Scientific research. Group: Signaling pathways. CAS No. 57018-04-9. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B2053. |  |
| Tolclofos-methyl (Standard) | Tolclofos-methyl (Standard) is the analytical standard of Tolclofos-methyl. This product is intended for research and analytical applications. Uses: Scientific research. Group: Signaling pathways. CAS No. 57018-04-9. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B2053R. | |
| Toldimfos sodium | Toldimfos sodium. Uses: Designed for use in research and industrial production. Additional or Alternative Names: sodium [4-(dimethylamino)-2-methylphenyl]phosphinate;TodlimfosSodium;4-Dimethylamino-o-tolyl phosphonous acid, sodium salt;Phosphinic acid, 4-(dimethylamino)-2-methylphenyl-, sodium salt;TOLDIMPHOSSODIUM;TONOPHOSPHAN;[2-Methyl-4-(dimethylamino)phenyl]phosphinic acid sodium salt;[4-(Dimethylamino)-2-methylphenyl]phosphinic acid sodium salt. CAS No. 575-75-7. Molecular formula: C9H13NNaO2P. Mole weight: 221.17. Purity: 95%+. IUPACName: sodium;[4-(dimethylamino)-2-methylphenyl]-oxido-oxophosphanium. Canonical SMILES: CC1=C(C=CC(=C1)N(C)C)[P+](=O)[O-].[Na+]. ECNumber: 209-391-4. Product ID: ACM575757. Alfa Chemistry ISO 9001:2015 Certified. Categories: Sodium (4-(dimethylamino)-2-methylphenyl)phosphinate. |  |
| Tolebrutinib | Tolebrutinib (SAR442168) is a potent, selective, orally active and brain-penetrant inhibitor of Bruton tyrosine kinase (BTK) , with IC 50 s of 0.4 and 0.7 nM in Ramos B cells and in HMC microglia cells, respectively. Tolebrutinib exhibits efficacy in central nervous system immunity. Tolebrutinib can be used for the research of multiple sclerosis (MS) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SAR442168; PRN2246. CAS No. 1971920-73-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109192. | |
| Tolfenamic Acid | Non-steroidal anti-inflammatory drugs (NSAIDs). Group: Biochemicals. Alternative Names: 2-[ (3-Chloro-2-methylphenyl) amino]benzoic Acid. Grades: Highly Purified. CAS No. 13710-19-5. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Tolfenamic Acid | Tolfenamic Acid (GEA 6414) is a non-steroidal anti-inflammatory and anti-cancer agent, selectively inhibits COX-2 , with an IC 50 of 13.49 μM (3.53 μg/mL) in LPS-treated (COX-2) canine DH82 monocyte/macrophage cells, but shows no effect on COX-1. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GEA 6414. CAS No. 13710-19-5. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0335. | |
| Tolfenamic acid-[13C6] | Tolfenamic acid-[13C6] is the labelled analogue of Tolfenamic acid, which is a non-steroidal anti-inflammatory drug (NSAID). It is a derivative of anthranilic acid, related structurally to Mefenamic and Flufenamic acids. Synonyms: 2-(3-Chloro-2-methyl-phenylamino)-13C6-benzoic acid; Tolfenamic acid-13C6; Tolfenamic Acid-(Benzoic ring-13C6); N-(3-Chloro-o-tolyl)anthranilic Acid-13C6; Clotam-13C6; Migea-13C6; N-(2-Methyl-3-chlorophenyl)anthranilic Acid-13C6; Tolfedine-13C6; Tolfine-13C6. Grade: 95% by HPLC; 98% atom 13C. CAS No. 1420043-61-3. Molecular formula: C8[13C]6H12ClNO2. Mole weight: 267.66. | |
| Tolfenamic Acid Acyl- β-D-Glucuronide Benzyl Ester | Protected Tolfenamic Acid Acyl- β-D-Glucuronide (T535310), a metabolite of Tolfenamic acid (T535300). Group: Biochemicals. Alternative Names: 1-[2-[ (3-Chloro-2-methylphenyl) amino]benzoate] β-D-Glucopyranuronic Acid Benzyl Ester. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Tolfenamic acid-(benzoic ring-13C6) | analytical standard. Group: Opiates / synthetic analgesic drug standards. | |
| Tolfenamic Acid-[d4] | Tolfenamic Acid-[d4] is the labelled analogue of Tolfenamic Acid, which is a non-steroidal anti-inflammatory drug (NSAID). It is a derivative of anthranilic acid, related structurally to Mefenamic and Flufenamic acids. Synonyms: Tolfenamic Acid D4; 2-[(3-Chloro-2-methylphenyl)amino]benzoic Acid-d4; N-(3-Chloro-o-tolyl)anthranilic Acid-d4; Clotam-d4; Migea-d4; N-(2-Methyl-3-chlorophenyl)anthranilic Acid-d4; Tolfedine-d4; Tolfine-d4. Grade: 98% by HPLC; 99% atom D. CAS No. 1246820-82-5. Molecular formula: C14H3D4ClNO2. Mole weight: 265.73. | |
| Tolfenamic Acid (Standard) | Tolfenamic Acid (Standard) is the analytical standard of Tolfenamic Acid. This product is intended for research and analytical applications. Tolfenamic Acid (GEA 6414) is a non-steroidal anti-inflammatory and anti-cancer agent, selectively inhibits COX-2 , with an IC 50 of 13.49 μM (3.53 μg/mL) in LPS-treated (COX-2) canine DH82 monocyte/macrophage cells, but shows no effect on COX-1. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GEA 6414 (Standard). CAS No. 13710-19-5. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0335R. | |
| Tolfenpyrad | Tolfenpyrad is an insecticide approved for marketing in Japan in 2002. Uses: Scientific research. Group: Signaling pathways. CAS No. 129558-76-5. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-17516. | |
| Tolinapant | Tolinapant (ASTX660) is an orally bioavailable dual antagonist of cellular inhibitor of apoptosis protein ( cIAP ) and X-linked inhibitor of apoptosis protein ( XIAP ). Uses: Scientific research. Group: Signaling pathways. Alternative Names: ASTX660. CAS No. 1799328-86-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109565. | |
| Toll Like Receptor 2, Positive Control (TLR2, TIL4, CD282) | Toll Like Receptor 2, Positive Control (TLR2, TIL4, CD282). Group: Molecular Biology. Pack Sizes: 15ul. US Biological Life Sciences. | Worldwide |
| Tolmetin | Tolmetin is an orally active and potent COX inhibitor with IC 50 s of 0.35 μM and 0.82 μM human COX-1 and COX-2, respectively. Tolmetin is a non-steroidal anti-inflammatory drug (NSAID) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 26171-23-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-B1799. | |
| Tolmetin-d3 | Anti-inflammatory. Group: Biochemicals. Alternative Names: 1-Methyl-d3-5-(4-methylbenzoyl)-1H-pyrrole-2-acetic Acid; 1-Methyl-d3-5-p-toluoylpyrrole-2-acetic Acid; 5-[(p-Tolyl)carbonyl]-1-methyl-d3-pyrrole-2-acetic Acid; McN 2559-d3; Tolmetine-d3. Grades: Highly Purified. CAS No. 1184998-16-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Tolmetin-d3 Ethyl Ester | Intermediate for the preparation of Isotope Labeled Tolmetin. Group: Biochemicals. Alternative Names: 1-Methyl-d3-5-(4-methylbenzoyl)-1H-pyrrole-2-acetic Acid Ethyl Ester. Grades: Highly Purified. CAS No. 1215579-60-4. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Tolmetin sodium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Tolmetin sodium dihydrate | Tolmetin sodium dihydrate is an orally active and potent COX inhibitor with IC 50 s of 0.35 μM and 0.82 μM human COX-1 and COX-2, respectively. Tolmetin sodium dihydrate is a non-steroidal anti-inflammatory drug (NSAID) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 64490-92-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1489. | |
| Tolmetin Sodium Salt Dihydrate | Anti-inflammatory. Group: Biochemicals. Alternative Names: 1-Methyl-5-(4-methylbenzoyl)-1H-pyrrole-2-acetic Acid Sodium Dihydrate; 1-Methyl-5-p-toluoylpyrrole-2-acetic Acid Sodium Dihydrate; 5-[(p-Tolyl)carbonyl]-1-methylpyrrole-2-acetic Acid Sodium Dihydrate; McN 2559-21-98; Tolectin; Tolmene. Grades: Highly Purified. CAS No. 64490-92-2. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Tolnaftate | Tolnaftate (NP-27) is a synthetic thiocarbamate used as an anti-fungal agent. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NP-27. CAS No. 2398-96-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0370. | |
| Tolnaftate | Tolnaftate (NP-27) is a synthetic thiocarbamate used as an anti-fungal agent. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Carbamothioic acid, N-methyl-N-(3-methylphenyl)-, O-2-naphthalenyl ester. Product Category: Inhibitors. Appearance: White powder. CAS No. 2398-96-1. Molecular formula: C19H17NOS. Mole weight: 307.41. Purity: 0.9994. Canonical SMILES: S=C(OC1=CC=C2C=CC=CC2=C1)N(C)C3=CC=CC(C)=C3. Density: 1.223 g/cm³. Product ID: ACM2398961. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tolnaftate | Antifungal. Group: Biochemicals. Alternative Names: N-Methyl-N- (3-methylphenyl) carbamothioic Acid O-2-Naphthalenyl Ester; Methyl (3-methylphenyl) carbamothioic Acid O-2-Naphthalenyl Ester; 2-Naphthyl N-Methyl-N-(3-tolyl)thiocarbamate. Grades: Highly Purified. CAS No. 2398-96-1. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Tolnaftate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: O-Naphthalen-2-yl methyl(3-methylphenyl)carbamothioate,Tolnaftate. | |
| Tolnaftate-d7 | Tolnaftate-d7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1329835-64-4. Molecular formula: C19H10D7NOS. Mole weight: 314.45. Catalog: APB1329835644. | |
| Tolnaftate-[d7] | Tolnaftate-[d7] is the labelled analogue of Tolnaftate, which could be used as an Antifungal agent. Synonyms: Tolnaftate D7; N-Methyl-N-(3-methylphenyl)carbamothioic Acid O-2-Naphthalenyl-d7 Ester. Grade: 95% by HPLC; 95% atom D. CAS No. 1329835-64-4. Molecular formula: C19H10D7NOS. Mole weight: 314.45. | |
| Tolnaftate Impurity 1 | Tolnaftate Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 10506-37-3. Molecular formula: C11H7ClOS. Mole weight: 222.69. Catalog: APB10506373. | |
| Tolnaftate Impurity 6 | Tolnaftate Impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 10103-06-7. Molecular formula: C12H12O2. Mole weight: 188.23. Catalog: APB10103067. | |
| Toloxatone | Toloxatone (MD 69276) is a reversible monoamine oxidase A ( MAO A ) inhibitor [1]. Antidepressant [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MD 69276. CAS No. 29218-27-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14196. | |
| Toloxatone | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| Tolperisone | Tolperisone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: AKOS 91983;1-piperidino-2-methyl-3-(p-tolyl)-3-propanone;2,4'-dimethyl-3-piperidino-propiophenon;2-methyl-3-piperidino-1-p-tolylpropan-1-one;mydeton;TOLPERISONE;2'4-Dimethyl-3-PiperidylPropiophenone;1-Propanone, 2-methyl-1-(4-methylphenyl)-3-(1-piperidin. Product Category: Heterocyclic Organic Compound. CAS No. 728-88-1. Molecular formula: C16H23NO. Mole weight: 245.36. Product ID: ACM728881. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tolperisone 4-carboxylic acid hydrochloride hydrate | Tolperisone 4-carboxylic acid hydrochloride hydrate. Group: Biochemicals. Alternative Names: 4-[2-Methyl-1-oxo-3- (1-piperidinyl) propyl]benzoic acid hydrochloride hydrate. Grades: Highly Purified. CAS No. 446063-44-1. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C16H26ClNO5. US Biological Life Sciences. | Worldwide |
| Tolperisone-[d10] Hydrochloride | Tolperisone-[d10] Hydrochloride is the labelled analogue of Tolperisone, which is an ion channel blocker and centrally-acting muscle relaxant. Synonyms: Tolperisone D10 Hydrochloride; 2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl-d10)-1-propanone Hydrochloride. Grade: 95% by HPLC; 98% atom D. CAS No. 1185160-65-9. Molecular formula: C16H13D10NOHCl. Mole weight: 291.88. | |
| Tolperisone hydrochloride | 25g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C16H23NO · HCl. CAS No. 3644-61-9. Prepack ID 23755666-25g. Molecular Weight 281.82. See USA prepack pricing. |  |
| Tolperisone hydrochloride | Tolperisone hydrochloride. Group: Biochemicals. Alternative Names: 2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl)-1-propanone hydrochloride; 2,4'-Dimethyl-3-piperidino-propiophenone hydrochloride; 2, 4'-Di methyl -3-piperidinopropiophenon e hydrochloride. Grades: Highly Purified. CAS No. 3644-61-9. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C16H24ClNO. US Biological Life Sciences. | Worldwide |
| Tolperisone hydrochloride | Tolperisone hydrochloride is a centrally acting muscle relaxant studied in neurological disorders causing pathological rhabdomyosclerosis (pyramidal tract injury, multiple sclerosis, myelopathy, encephalomyelitis), spastic paralysis, and other muscle dystonia-related Encephalopathy. Tolperisone hydrochloride also has antiviral activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3644-61-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B1139. | |
| Tolperisone Hydrochloride | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopyapi standardspharmaceutical toxicology. Alternative Names: 1-Propanone, 2-methyl-1-(4-methylphenyl)-3-(1-piperidinyl)-, hydrochloride (9CI), 1-Piperidino-2-methyl-3-(4-methylphenyl)propan-3-one hydrochloride, Atmosgen, Arantoick, Metosomin, Tolfree, Isocalm, Tolisartine, Tolpidol, Naismeritin, Midocalm, Biocalm, Kineorl, Abbsa, Menopatol, Tolperisone hydrochloride, 2,4'-Dimethyl-3-piperidinopropiophenone hydrochloride, Propiophenone, 2,4'-dimethyl-3-piperidino-, hydrochloride (7CI,8CI), Minacalm, N 553, Mydocalm, Besnoline, Muscalm,2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl)-1-propanone Hydrochloride (1:1). | |
| Tolperisone Hydrochloride (2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl)-1-propanone) | Used as a muscle relaxant. Group: Biochemicals. Alternative Names: 2-Methyl-1-(4-methylphenyl)-3-(1-piperidinyl)-1-propanone. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Tolpropamine | Tolpropamine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3-dimethylamino-1-phenyl-1-p-tolylpropane;dimethyl(3-phenyl-3-p-tolylpropyl)amine;tolpropamine;N,N-Dimethyl-3-phenyl-3-(p-tolyl)-1-propanamine;N,N-Dimethyl-3-phenyl-3-p-tolyl-1-propanamine. Product Category: Heterocyclic Organic Compound. CAS No. 5632-44-0. Molecular formula: C18H23N. Mole weight: 253.382. Product ID: ACM5632440. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tolrestat | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopyenzyme activators, inhibitors & substrates. Alternative Names: N-[[6-Methoxy-5-(trifluoromethyl)-1-naphthalenyl]thioxomethyl]-N-methylglycine, Tolrestat, Lorestat,Glycine, N-[[6-methoxy-5-(trifluoromethyl)-1-naphthalenyl]thioxomethyl]-N-methyl-, Tolrestatin, AY 27773, Alredase. | |
| Tolterodine | Tolterodine(PNU-200583) is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (R)-(+)-Tolterodine; (+)-Tolterodine; (R)-Tolterodine; PNU-200583. CAS No. 124937-51-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0024. | |
| Tolterodine-d14 hydrochloride | Tolterodine-d 14 (hydrochloride) is the deuterium labeled Tolterodine hydrochloride[1]. Tolterodine hydrochloride is a potent muscarinic receptor antagonist[2][3]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: (R)-(+)-Tolterodine-d14 hydrochloride; (+)-Tolterodine-d14 hydrochloride; (R)-Tolterodine-d14 hydrochloride; PNU-200583-d14 hydrochloride. CAS No. 1217645-16-3. Pack Sizes: 1 mg. Product ID: HY-A0024S. | |
| Tolterodine impurity 1 | Tolterodine impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 124936-82-9. Molecular formula: C22H31NO. Mole weight: 325.5. Catalog: APB124936829. | |
| Tolterodine L-tartrate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Tolterodine S-Enantiomer | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Tolterodine System Suitability Mixture | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Tolterodine tartrate | Tolterodine tartrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 124937-52-6. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. US Biological Life Sciences. | Worldwide |
| Tolterodine tartrate | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C22H31NO · C4H6O6. CAS No. 124937-52-6. Prepack ID 51586860-1g. Molecular Weight 475.57448. See USA prepack pricing. | |
| Tolterodine tartrate | Tolterodine Tartrate (Kabi-2234; PNU-200583E) is a potent muscarinic receptor antagonist and shows selectivity for the urinary bladder over salivary glands in vivo. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Kabi-2234; PNU-200583E. CAS No. 124937-52-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-90010. | |
| Tolterodine Tartrate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: 2-[(1R)-3-[Bis(1-methylethyl)amino]-1-phenylpropyl]-4-methylphenol (2R,3R)-2,3-dihydroxybutanedioate (1:1), PNU 200583E, Tolterodine L-tartrate, (R)-(+)-N,N-Diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenylpropylamine L-tartrate, Detrol, Detrusitol,Tolterodine Tartrate, Tolterodinium (+)-(2R,3R)-hydrogen tartrate (1:1), (R)-2-[3-[Bis(1-methylethyl)amino]-1-phenylpropyl]-4-methylphenol [R-(R*,R*)]-2,3-dihydroxybutanedioate (1:1) (salt), Tolterodine tartrate, (R)-Tolterodine L-tartrate. | |
| Tolterodine Tartrate EP Impurity A | Tolterodine Tartrate EP Impurity A. Uses: For analytical and research use. Group: Impurity standards. CAS No. 124937-73-1. Molecular formula: C17H20O2. Mole weight: 256.35. Catalog: APB124937731. | |
| Tolterodine Tartrate EP Impurity F | Tolterodine Tartrate EP Impurity F. Uses: For analytical and research use. Group: Impurity standards. CAS No. 124937-53-7. Molecular formula: C22H31NO. Mole weight: 325.5. Catalog: APB124937537. | |
| Tolterodine, Tartrate (PNU-20058E, Detrol, Detrusitol) | A muscarinic receptor antagonist. Used in the treatment of urinary incontinence. Group: Biochemicals. Alternative Names: PNU-20058E, Detrol, Detrusitol. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Toltrazuril | A triazinetrione anticoccidial. Coccidiostat. Group: Biochemicals. Alternative Names: 1-Methyl-3-[3-methyl-4-[4-[ (trifluoromethyl) thio]phenoxy]phenyl]-1, 3, 5-triazine-2, 4, 6 (1H, 3H, 5H) -trione; BAY-Vi 9142; Baycox. Grades: Highly Purified. CAS No. 69004-03-1. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C??H??F?N?O?S, Molecular Weight: 425.38. US Biological Life Sciences. | Worldwide |
| Toltrazuril | Toltrazuril (BAY-i 9142) is an antiprotozoal agent that acts upon Coccidia parasites. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY-i 9142. CAS No. 69004-03-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0175. | |
| Toltrazuril | Toltrazuril can be used to treat poultry coccidiosis. Synonyms: Baycox; Toltrazurilo; Toltrazurilum. Grade: >98%. CAS No. 69004-03-1. Molecular formula: C18H14F3N3O4S. Mole weight: 425.38. | |
| Toltrazuril | Toltrazuril (BAY-i 9142) is an antiprotozoal agent that acts upon Coccidia parasites. Uses: Designed for use in research and industrial production. Additional or Alternative Names: bay-i9142;TOLTRAZURIL;BAYCOX;1-METHYL-3-[3-METHYL-4-[4-(TRIFLUOROMETHYLTHIO)PHENOXY]PHENYL]-1,3,5-TRIAZINE-2,4,6(1H,3H,5H)-TRIONE;Bayvi 9142;MARIGOLD OLEORESIN;Toltarzuril;Toltrazuril98-102%. Product Category: Inhibitors. CAS No. 69004-03-1. Molecular formula: C18H14F3N3O4S. Mole weight: 425.38. Purity: 0.9964. Product ID: ACM69004031. Alfa Chemistry ISO 9001:2015 Certified. | |
| Toltrazuril 98% HPLC | Toltrazuril 98% HPLC. |  CA, FL & NJ |
| Toltrazuril-[d3] | Toltrazuril-[d3] is the labelled analogue of Toltrazuril. Toltrazuril has been found to be an antiprotazoal agent and could be used against Equine Protozoal Myeloencephalitis. Synonyms: Toltrazuril D3; 1-Methyl-3-[3-methyl-4-[4-[(trifluoromethyl)thio]phenoxy]phenyl]-1,3,5-triazine-2,4,6(1H,3H,5H)-trione-d3. Grade: 95% by HPLC; 98% atom D. CAS No. 1353867-75-0. Molecular formula: C18H11D3F3N3O4S. Mole weight: 428.4. | |
| Toltrazuril-(N-methyl-d3) | analytical standard. Group: Application areas. | |
| Toltrazuril sulfone | analytical standard. Group: Application areas. | |
| Toltrazuril (sulfone) | Toltrazuril sulfone (Ponazuril) is a metabolite of Toltrazuril (HY-B0175), with antiprotozoal activity. Toltrazuril sulfone is a triazine anticoccidial that is developed to prevent coccidiosis in poultry[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ponazuril. CAS No. 69004-04-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-17008. | |
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