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| Product | Description | |
|---|---|---|
| Cyclotide C, partial | Cyclotide C, partial is isolated from Viola odorata. It has antimicrobial activity. |  |
| Cyclotide vibi-E | Cyclotide vibi-E is produced by Viola biflora. It probably participates in a plant defense mechanism. Cyclotide vibi-E has cytotoxic activity, active against a human lymphoma cell line with an IC50 of 3.2 μM. | |
| Cyclotide vibi-H | Cyclotide vibi-H is produced by Viola biflora. It has antimicrobial and anticancer activity. | |
| Cyclotraxin B | Cyclotraxin B is a selective and potent Trk B (BDNF/NT-3) receptor inhibitor with an IC50 value of 0.30 nM. It prevents receptor activation by BDNF without interfering with BDNF binding. It sometimes fused with tat-protein for increased brain permeability in rodent studies. It has been shown to exhibit putative anxiolytic properties in mice. It prevents cold allodynia induced by BDNF in mice and reduces cocaine self-administration. Synonyms: L-Cysteinyl-L-asparaginyl-L-prolyl-L-methionylglycyl-L-tyrosyl-L-threonyl-L-lysyl-L-a-glutamylglycyl-L-cysteine, cyclic (1>11)-disulfide. Grade: >98%. CAS No. 1203586-72-4. Molecular formula: C48H73N13O17S3. Mole weight: 1200.36. | |
| Cyclotraxin B | Cyclotraxin B. Group: Biochemicals. Grades: Purified. CAS No. 1203586-72-4. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Cyclotraxin B | Cyclotraxin B is a BBB-penetrable and selective TrkB inhibitor. Cyclotraxin B inhibits BDNF-induced TrkB activity in a non-competitive manner, with an IC50 of 0.30 nM. Cyclotraxin B has analgesic and anxiolytic effects[1][2][3]. Uses: Scientific research. Group: Peptides. CAS No. 1203586-72-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1178. |  |
| Cyclotraxin B acetate | Cyclotraxin B is a selective and potent Trk B (BDNF/NT-3) receptor inhibitor with an IC50 value of 0.30 nM. It prevents receptor activation by BDNF without interfering with BDNF binding. Molecular formula: C50H77N13O19S3. Mole weight: 1260.42. | |
| Cyclotraxin-B trifluoroacetate salt | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Cyclotriazadisulfonamide | Cyclotriazadisulfonamide is a CD4-targeted HIV entry inhibitor. CADA inhibits HIV at submicromolar levels by specifically down-modulating cell-surface and intracellular CD4. Synonyms: CADA; 9-benzyl-3-methylene-1,5-bis(p-tolylsulfonyl)-1,5,9-triazacyclododecane. Grade: >98%. CAS No. 182316-44-5. Molecular formula: C31H39N3O4S2. Mole weight: 581.79. | |
| Cyclotriphosphazene-pmmh-6 dendrimer generation 1.0 | Cyclotriphosphazene-pmmh-6 dendrimer generation 1.0. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CYCLOTRIPHOSPHAZENE-PMMH-6 DENDRIMER GENERATION 1.0. Product Category: Nanoparticles & Nanopowders. CAS No. 189939-11-5. Molecular formula: C48 H48 Cl12 N15 O6 P9 S6. Mole weight: 1827.6. Product ID: ACM189939115. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Cyclo(tyr-ile-gln-asn-asu)-pro-arg-gly-nh2 | Cyclo(tyr-ile-gln-asn-asu)-pro-arg-gly-nh2. Uses: Designed for use in research and industrial production. Additional or Alternative Names: [ASU1,6,ARG8] VASOTOCIN;CYCLO(TYR-ILE-GLN-ASN-ASU)-PRO-ARG-GLY-NH2;DEAMINO-DICARBA-ARGININE-VASOTOCIN;DEAMINO-DICARBA-ARG-VASOTOCIN;TYR-ILE-GLN-ASN-ASU-PRO-ARG-GLY-NH2;vasopressin (Asu1,6,Arg8). Product Category: Heterocyclic Organic Compound. CAS No. 35375-13-4. Molecular formula: C45H70N14O12. Mole weight: 999.12. Purity: 0.96. IUPACName: (2S)-N-[(2S)-1-[(2-amino-2-oxoethyl)amino]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]-1-[(2S,5S,8S,11S,14S)-11-(2-amino-2-oxoethyl)-8-(3-amino-3-oxopropyl)-5-[(2S)-butan-2-yl]-2-[(4-hydroxyphenyl)methyl]-3,6,9,12,20-pentaoxo-1,4,7,10,13-pentazacycloico. Canonical SMILES: CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(CCCCCC(=O)NC(C(=O)N1)CC2=CC=C(C=C2)O)C(=O)N3CCCC3C(=O)NC(CCCN=C(N)N)C(=O)NCC(=O)N)CC(=O)N)CCC(=O)N. Product ID: ACM35375134. Alfa Chemistry ISO 9001:2015 Certified. Categories: [1,6-Aminosuberic acid]-arginine-Vasotocin. | |
| Cycloundecanecarboxylic acid | Cycloundecanecarboxylic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CYCLOUNDECANECARBOXYLIC ACID. Product Category: Heterocyclic Organic Compound. CAS No. 831-67-4. Molecular formula: C12H22O2. Mole weight: 198.3. Purity: 0.96. IUPACName: cycloundecanecarboxylic acid. Canonical SMILES: C1CCCCCC(CCCC1)C(=O)O. Density: 0.956g/cm³. ECNumber: 212-609-0. Product ID: ACM831674. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cycloviolacin H2 | Cycloviolacin H2 is produced by Viola hederacea. It probably participates in a plant defense mechanism. | |
| Cycloviolacin H3 | Cycloviolacin H3 is produced by Viola hederacea. It probably participates in a plant defense mechanism. | |
| Cycloviolacin H4 | Cycloviolacin H4, a hydrophobic cyclotide from Viola hederaceae. Cycloviolacin H4 exhibits the most potent hemolytic activity in cyclotides reported so far, and this activity correlates with the size of a surface-exposed hydrophobic patch. Synonyms: cycloviolacin H4; CHEMBL499782. Molecular formula: C132H200N34O41S6. Mole weight: 3111.6. | |
| Cycloviolacin O1 | Cycloviolacin O1 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O13 | Cycloviolacin O13 is produced by Viola odorata. It probably participates in a plant defense mechanism. Cycloviolacin O13 has hemolytic activity. Molecular formula: C133H207N37O38S6. Mole weight: 3124.67. | |
| Cycloviolacin O14 | Cycloviolacin O14 is produced by Viola odorata. It probably participates in a plant defense mechanism. Cycloviolacin O14 has hemolytic activity. Molecular formula: C132H197N35O41S6. Mole weight: 3122.57. | |
| Cycloviolacin O15 | Cycloviolacin O15 is produced by Viola odorata. It probably participates in a plant defense mechanism. Cycloviolacin O15 has hemolytic activity. Molecular formula: C130H195N33O39S6. Mole weight: 3036.52. | |
| Cycloviolacin O16 | Cycloviolacin O16 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O17 | Cycloviolacin O17 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O18 | Cycloviolacin O18 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O19 | Cycloviolacin O19 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin-O2 | Cycloviolacin-O2 is isolated from Viola odorata. It probably participates in a plant defense mechanism. Cycloviolacin-O2 has strong cytotoxic activity against a variety of drug-resistant and drug-sensitive human tumor cell lines, and against primary chronic lymphocytic leukemia and ovarian carcinoma cells. It also has weaker cytotoxic activity against normal lymphocytes and hemolytic activity. Synonyms: Cycloviolacin-O2; IHB9R8ET7W; CHEMBL4210529; cycloviolacin O2; 261714-23-2; Cyclo(Gly-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Trp-Ile-Pro-Cys-Ile-Ser-Ser-Ala-Ile-Gly-Cys-Ser-Cys-Lys-Ser-Lys-Val-Cys-Tyr-Arg-Asn) 4->18,6->22, 11->27 trisdisulfide; UNII-IHB9R8ET7W; CHEMBL4285275; BDBM50452159. CAS No. 261714-23-2. Molecular formula: C133H207N37O39S6. Mole weight: 3140.7. | |
| Cycloviolacin O20 | Cycloviolacin O20 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O21 | Cycloviolacin O21 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O22 | Cycloviolacin O22 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O23 | Cycloviolacin O23 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O24 | Cycloviolacin O24 is produced by Viola odorata. It probably participates in a plant defense mechanism. Molecular formula: C126H179N35O42S6. Mole weight: 3048.36. | |
| Cycloviolacin O25 | Cycloviolacin O25 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O3 | Cycloviolacin O3 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin O8 | Cycloviolacin O8 is produced by Viola odorata. It probably participates in a plant defense mechanism. | |
| Cycloviolacin Y1 | Cycloviolacin Y1 was found in Viola yedoensis. It has anti-HIV activity (EC50=1.2 microM). Synonyms: Cycloviolacin Y1. Molecular formula: C144H206N36O48S6. Mole weight: 3401.8. | |
| Cycloviolacin Y2 | Cycloviolacin Y2 was found in Viola philippica. It has antiviral activity. | |
| Cycloviolacin Y3 | Cycloviolacin Y3 was found in Viola philippica. It has antiviral activity. | |
| Cycloviolacin Y4 | Cycloviolacin Y4 was found in Viola yedoensis. It has anti-HIV activity (EC50=0.12 microM). Molecular formula: C127H202N32O41S6. Mole weight: 3025.53. | |
| Cycloviolacin Y5 | Cycloviolacin Y5 was found in Viola philippica. It has antiviral activity. Synonyms: Cycloviolacin Y5. Molecular formula: C132H209N33O42S6. Mole weight: 3122.7. | |
| Cycloviolin-A | Cycloviolin-A is isolated from Leonia cymosa. It probably participates in a plant defense mechanism. Cycloviolin-A has anti-HIV activity. Molecular formula: C137H216N38O39S6. Mole weight: 3211.79. | |
| Cycloviolin-B | Cycloviolin-B is isolated from Leonia cymosa. It probably participates in a plant defense mechanism. Cycloviolin-B has anti-HIV activity. Molecular formula: C120H177N31O40S6. Mole weight: 2886.26. | |
| Cycloviolin-C | Cycloviolin-C is isolated from Leonia cymosa. It probably participates in a plant defense mechanism. Cycloviolin-C has anti-HIV activity. Molecular formula: C133H209N37O39S6. Mole weight: 3142.69. | |
| Cycloviolin-D | Cycloviolin-D is isolated from Leonia cymosa. It probably participates in a plant defense mechanism. Cycloviolin-D has anti-HIV activity. Molecular formula: C135H205N37O38S6. Mole weight: 3146.68. | |
| Cycloviracin B1 | Cycloviracin B1 is produced by the strain of Kibdelosporangium albatum sp. R761-7. It has anti-herpes simplex virus Type I (HSV-1) activity and has weak anti-gram-positive bacterial activity. Synonyms: (1S,3R,8R,9S,10S,11S,12R,14R,19S,20S,21R,22S)-3-((16R)-16,22-bis(((2S,3R,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-methoxytetrahydro-2H-pyran-2-yl)oxy)tricosyl)-14-(14-(((2S,3R,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-methoxytetrahydro-2H-pyran-2-yl)oxy)-20-hydroxyhenicosyl)-9,10,11,20,21,22-hexahydroxy-2,6,13,17,23,24-hexaoxatricyclo[17.3.1.18,12]tetracosane-5,16-dione. CAS No. 142382-45-4. Molecular formula: C83H152O33. Mole weight: 1678.07. | |
| Cycloviracin B2 | Cycloviracin B2 is produced by the strain of Kibdelosporangium albatum sp. R761-7. It has anti-herpes simplex virus Type I (HSV-1) activity and has weak anti-gram-positive bacterial activity. CAS No. 142382-46-5. Molecular formula: C83H150O33. Mole weight: 1676.06. | |
| Cyclovirobuxine D | Cyclovirobuxine D - Product ID: NST-10-225. Category: Terpenes. Purity: 98%. Test method: HPLC. CAS No. 860-79-7. Pack Sizes: 0,05g, 0,1g, 0,25g, 0,5g. Appearance: Yellow Powder. Molecular formula: C26H46N2O. Mole weight: 402.7. Storage: +2 +8 °C. |  |
| Cyclovirobuxine D | Cyclovirobuxine D. Group: Biochemicals. Grades: Plant Grade. CAS No. 860-79-7. Pack Sizes: 20mg. Molecular Formula: C26H46N2O, Molecular Weight: 402.66. US Biological Life Sciences. | Worldwide |
| Cycloxidim | analytical standard. Group: Pesticides & metabolites standards. | |
| Cycloxydim | Cycloxydim. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (+-)-2-(1-(ethoxyimino)butyl)-3-hydroxy-5-thian-3-cyclohex-2-enone;2-(1-(ethoxyimino)butyl)-3-hydroxy-5-(tetrahydro-2h-thiopyran-3-yl)-2-cycloh;2-cyclohexen-1-one,2-(1-(ethoxyimino)butyl)-3-hydroxy-5-(tetrahydro-2h-thiopyr;2-cyclohexen-1-one,2-[1-(ethoxy. Product Category: Heterocyclic Organic Compound. CAS No. 101205-02-1. Molecular formula: C17H27NO3S. Mole weight: 325.47. Product ID: ACM101205021. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cyclozonal | Cyclozonal. CAS No. 68991-97-9. VIGON Item # 507439. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| CycLuc1 | CycLuc1 is a blood-brain barrier permeable luciferase substrate that displays near-infrared (NIR) emission with a peak luminescence wavelength of 599 nm. CycLuc1 can be used for in vivo bioluminescence imaging[1][2]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 1247879-16-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111653. | |
| Cycluron | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Cycoloy | Cycoloy. Group: Polymers. |  |
| Cycrimine | Cycrimine is an orally active muscarinic cholinergic receptor (mAChR) M1 antagonist, reduces the acetylcholine levels in parkinson model. Cycrimine shows antispasmodic activity, can be used in studies of behavioral and mental disorder [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 77-39-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-119918. | |
| CYD19 | CYD19 is a potent Snail/HDAC dual target inhibitor. CYD19 displays potent inhibitory activity against HDAC1 with an IC50 of 0.405 ?M and potent inhibition against Snail with a Kd of 0.18 ?M. CYD19 increases histone H4 acetylation in HCT-116 cells and decreases the expression of Snail protein to induce cell apoptosis[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Snail/HDAC-IN-1. CAS No. 2415281-52-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-144315. | |
| Cyflaural Givco 120/20/2 | Cyflaural Givco 120/20/2. CAS No. MIXTURE. VIGON Item # 508451. Categories: Speciality Ingrdients Suppliers. | America & Internationally |
| Cyflufenamid | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Cyflumetofen | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Cyflumetofen | Cyflumetofen. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CYFLUMETOFEN;2-Methoxyethyl (rs)-2-(4-tert-butylphenyl)-2-cyano-3-oxo-3-(alpha,alpha,alpha-trifluoro-o-tolyl)propionate;Cyflumetofen [iso];alpha-Cyano-alpha-[4-(1,1-dimethylethyl)phenyl]-beta-oxo-2-(trifluoromethyl)benzenepropanoic acid 2-methoxyethyl ester;2-Methoxyethyl (RS)-2-(4-tert-butylphenyl)-2-cyano-3-oxo-3-(α,α,α-trifluoro-o-tolyl)propionate. CAS No. 400882-07-7. Molecular formula: C24H24F3NO4. Mole weight: 447.451. Purity: 0.95. IUPACName: 2-methoxyethyl2-(4-tert-butylphenyl)-2-cyano-3-oxo-3-[2-(trifluoromethyl)phenyl]propanoate. Canonical SMILES: CC(C)(C)C1=CC=C(C=C1)C(C#N)(C(=O)C2=CC=CC=C2C(F)(F)F)C(=O)OCCOC. Density: 1.214. Product ID: ACM400882077. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cyfluthrin | Cyfluthrin is a class II Pyrethroid, with effects on the sodium current, especially late sodium current (INa-L). Uses: Insecticides. Synonyms: CYFLUTHRIN; Baythroid; beta-Cyfluthrin. CAS No. 68359-37-5. Molecular formula: C22H18Cl2FNO3. Mole weight: 434.29. | |
| Cyfluthrin | Cyfluthrin is a type II pyrethroid and has effects on various insects. Cyfluthrin is a modulator of Nav 1.8 sodium channels by repetitive stimulation. Cyfluthrin can be applied in agriculture,veterinary, insecticide,pyrethroid and stored product [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 68359-37-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B1837. | |
| CyflutHrin, Mixture of isomers, TecHnical grade Technical grade | CyflutHrin, Mixture of isomers, TecHnical grade Technical grade. Group: Biochemicals. Grades: Purified. CAS No. 68359-37-5. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Cyfluthrin Phenoxy-d5 | Cyfluthrin Phenoxy-d5 is the deuterized or labeled form of β-Cyfluthrin (C989510), which is a synthetic pyrethroid insectide and common household pesticide. It is highly toxic to fish, invertebrates, and insects, but it is far less toxic to humans. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C22H13D5Cl2FNO3, Molecular Weight: 439.32. US Biological Life Sciences. | Worldwide |
| CYH33 methanesulfonate | CYH33 methanesulfonate is an orally active, highly selective PI3Kα inhibitor with IC50s of 5.9 nM/598 nM/78.7 nM/225 nM against α/β/δ/γ isoform, respectively. CYH33 methanesulfonate has potent activity against solid tumors. Synonyms: CYH 33 methanesulfonate; Carbamic acid, N-(5-(6-((4-(methylsulfonyl)-1-piperazinyl)methyl)-4-(4-morpholinyl)pyrrolo(2,1-F)(1,2,4)triazin-2-yl)-4-(trifluoromethyl)-2-pyridinyl)-, methyl ester, methanesulfonate (1:1). CAS No. 1494684-33-1. Molecular formula: C25H33F3N8O8S2. Mole weight: 694.70. | |
| Cyhalofop | Cyhalofop(Cyhalofop acid) is a recently registered herbicide from the aryloxyphenoxy propionate group in India to control a wide range of grass weed species at various growth stages in rice crop. Synonyms: Cyhalofop acid. Grade: >98%. CAS No. 122008-78-0. Molecular formula: C16H12FNO4. Mole weight: 301.27. | |
| Cyhalofop | Cyhalofop (Cyhalofop acid), the primary metabolite of Cyhalofop-butyl (HY-B0861) in susceptible grasses, is the herbicidally active metabolite. Cyhalofop-butyl is an aryloxyphenoxypropionate post-emergence herbicide widely used around the world in agriculture [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cyhalofop acid. CAS No. 122008-78-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-17528. | |
| Cyhalofop-butyl | Cyhalofop-butyl is a post-emergence herbicide. Cyhalofop-butyl inhibits acetyl-coenzyme A carboxylase ( ACCase ) biosynthesis [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 122008-85-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0861. | |
| Cyhalofop-butyl | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Cyhalofop Butyl | Cyhalofop Butyl. Group: Biochemicals. Alternative Names: Butyl (R) -2-[4- (4-Cyano-2-fluorophenoxy) phenoxy]propionate; (R) -2-[4- (4-Cyano-2-fluorophenoxy) phenoxy]propionic Acid Butyl Ester. Grades: Highly Purified. CAS No. 122008-85-9. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| Cyhalothrin solution | 100 ?g/mL in acetonitrile, analytical standard. Group: Method and regulation specific. | |
| Cyheptamide | Cyheptamide is an analogue of Carbamazepine which is used in treatment of pain associated with trigeminal neuralgia. Synonyms: 10,11-Dihydro-5H-dibenzo[a,d]cycloheptene-5-carboxamide; AY 8682; BS 7029; Carbamazepam; ICI 51426. CAS No. 7199-29-3. Molecular formula: C16H15NO. Mole weight: 237.30. | |
| Cyheptamide | An analogue of Carbamazepine. The toxicity of Cyheptamide in mice and rats is very low, and anticonvulsant activity is marked. Carbamazepine and Cyheptamide have certain stereochemical features in common with Phenytoin. Group: Biochemicals. Alternative Names: 10, 11-Dihydro-5H-dibenzo[a, d]cycloheptene-5-carboxamide; AY 8682; BS 7029; Carbamazepam; ICI 51426. Grades: Highly Purified. CAS No. 7199-29-3. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
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