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| Product | Description | |
|---|---|---|
| Lead Sulfate | Lead Sulfate. Group: Biochemicals. Alternative Names: Lead(II) sulfate. Grades: Highly Purified. CAS No. 7446-14-2. Pack Sizes: 250g, 500g, 1kg, 2kg. US Biological Life Sciences. |  Worldwide |
| Lead Sulfate 98+% | Lead Sulfate 98+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100g, 500g, 1Kg, 2.5Kg. US Biological Life Sciences. | Worldwide |
| Lead sulfate basic | Heterocyclic Organic Compound. Alternative Names: Leadoxidesulfate; leadoxidesulfate(pb2o(so4)); LEAD(II) SULFATE, TRIBASIC;LEAD SULFATE;LEAD SULFATE(II);LEAD(+2)SULFATE;lead sulphate, basic;Lead(?) sulfate tribasic. CAS No. 12036-76-9. Molecular formula: PbO.PbSO4. Mole weight: 526.462. Purity: Basic. IUPACName: lead(2+); oxolead; sulfate. Canonical SMILES: [O-]S(=O)(=O)[O-].O=[Pb].[Pb+2]. Density: 6.2 g/mL at 25 °C(lit.). ECNumber: 234-853-7. Catalog: ACM12036769. |  |
| Lead sulfate tribasic | Heterocyclic Organic Compound. Alternative Names: Tribasic lead sulfate(Pb4O3(SO4)). CAS No. 12202-17-4. Molecular formula: Pb4SO7. Mole weight: 972.86. Appearance: white or off-white powder. Density: 6.9. Catalog: ACM12202174. | |
| Lead (II) Sulfate | LEAD (II) SULFATE, 99% pure, -150 mesh, Formula: PbSO4. CAS No. 7446-14-2. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Lead (II) Sulfate | LEAD (II) SULFATE, 99% pure, -60 mesh, Formula: PbSO4. CAS No. 7446-14-2. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Lead (II) Sulfate | Lead (II) Sulfate. Grades: 98.% Very High (95-98%). CAS No. 7446-14-2. Pack Sizes: Kilogram Quanitites: 10 kg , 50 kg. Order Number: 2287. |  www.prochemonline.com |
| Tribasic Lead Sulfate | Heterocyclic Organic Compound. Alternative Names: Lead hydroxide oxide sulfate;Tribasic Lead Sulfate. CAS No. 11083-39-9. Molecular formula: Pb4(OH)2O2(SO4). Mole weight: 990.87. Catalog: ACM11083399. | |
| Tribasic Lead Sulfate | Tribasic Lead Sulfate. Group: Polymerspvc stabilizers. |  |
| 1-Butyl-4-methylpyridinium tetrafluoroborate | 4MBPBF4 has been used in the preparation of the SWNT-polymer composite films to improve the dispersion of SWNTs and conductivity of the composites (SWNT= singlewalled carbon nanotubes). The use of 4MBPBF4 as a reaction media during derivatization of dimethyl sulfate with dibenzazepine, accelerates the rate of the reaction. It can also be used to modify carbon paste electrode, which leads to high sensitivity, selectivity and low detection limit for both potassium ferricyanide and dopamine by cyclic voltammetric technique. Group: Electrolytesbattery materials. Alternative Names: 1-Butyl-4-picoliniumtetrafluoroborate,4MBPBF4. CAS No. 343952-33-0. Product ID: 1-butyl-4-methylpyridin-1-ium; tetrafluoroborate. Molecular formula: 237.05. Mole weight: C10H16BF4N. [B-](F)(F)(F)F.CCCC[N+]1=CC=C(C=C1)C. 1S/C10H16N. BF4/c1-3-4-7-11-8-5-10(2)6-9-11; 2-1(3, 4)5/h5-6, 8-9H, 3-4, 7H2, 1-2H3; /q+1; -1. VISYYHYJMCAKAF-UHFFFAOYSA-N. ≥97.0%(T). | |
| Noah Chemicals | Noah Chemicals is your single source for both traditional and custom chemical products. Whether you are in need of a regularly produced inorganic compound or a rare or custom-manufactured chemical, Noah Chemicals has the facilities and the expertise to meet your requirements. Product range includes: Barium Acetate, Barium Sulfate, Iron (II) Chloride, Lanthanum Nitrate, Lead (II) Nitrate, Silicon Carbide, Strontium Acetate, Tin (II) Fluoride, Titanium (IV) Isopropoxide, Zirconium Hydroxide.featured listing | Texas TX |
| Coptisine sulfate | Coptisine sulfate is a natural compound that belongs to the group of plant alkaloids. It has been shown to have anti-inflammatory properties, significant cytotoxicity, and significant mitochondrial membrane potential in myeloma cells. Coptisine sulfate inhibits toll-like receptor 4 (TLR4), which is a protein present on the surface of immune cells. Coptisine sulfate has been shown to inhibit the production of cytokines such as tumor necrosis factor alpha (TNF-α) and IL-6 by these cells. Coptisine sulfate also inhibits the activation of nuclear factor kappa B (NFκB) and mitogen activated protein kinase (MAPK). This inhibition leads to reduced levels of proinflammatory cytokines and chemokines, such as IL-1β, IL-8, MCP1, and GRO&alpha. Group: Other alkaloids. CAS No. 1198398-71-8. Molecular formula: C38H28N2O12S. Mole weight: 736.7 g/mol. Canonical SMILES: C1C[N+]2=C (C=C3C=CC4=C (C3=C2)OCO4)C5=CC6=C (C=C51)OCO6. Catalog: ACM1198398718. | |
| Docusate Sodium | Docusate Sodium (Dioctyl sulfosuccinate sodium salt) is one of the main components in stool softeners. Docusate Sodium is a sulfated surfactant and may inactivate viral pathogens by disrupting viral envelopes and/or denaturing/disassociating proteins. Docusate Sodium is effective in vitro against wild type and drug-resistant strains of HSV type 1 and 2. Docusate Sodium is an obesogen. Docusate Sodium with developmental exposure leads to increased adult adiposity, inflammation, metabolic disorder and dyslipidemia in offspring fed a standard diet in mice [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Dioctyl sulfosuccinate sodium salt. CAS No. 577-11-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1268. |  |
| Evodiamine | Evodiamine is a natural compound with apoptotic activity. It has been found to induce apoptosis in human osteosarcoma cells by binding to pro-apoptotic protein, leading to the activation of caspases and downregulation of Bcl-2. Evodiamine also has synergistic effects with other drugs that induce apoptosis, such as dextran sulfate, an anticancer drug. This compound has shown promising results in clinical trials for breast cancer and resistant breast cancer. The mechanism of action of evodiamine is not fully understood but it may involve autophagy or the induction of plate test. Evodiamine may also have anti-infectious properties due to its ability to inhibit bacteria growth by interfering with DNA binding activity and protein synthesis. Group: Other alkaloids. CAS No. 518-17-2. Molecular formula: C19H17N3O. Mole weight: 303.36 g/mol. Canonical SMILES: CN1[C@@H]2C3=C (CCN2C (=O)C4=CC=CC=C41)C5=CC=CC=C5N3. Catalog: ACM518172. | |
| Larotrectinib Sulfate (ARRY 470, LOXO 101) | A potent ATP-competitive inhibitor of tropomyosin-related kinases (TRK1, TRK2 and TRK3), members of the receptor tyrosine kinase family of neurotrophin receptors. Tumors with oncogenic TRK fusions are sensitive to larotrectinib, leading to reduced proliferation and tumor growth in patients with soft tissue sarcoma, triple-negative breast cancer and lung cancer.A potent ATP-competitive inhibitor of tropomyosin-related kinases (TRK1, TRK2 and TRK3), members of the receptor tyrosine kinase family of neurotrophin receptors. Tumors with oncogenic TRK fusions are sensitive to larotrectinib, leading to reduced proliferation and tumor growth in patients with soft tissue sarcoma,...odels. The TRK family of neurotrophin receptors, TRKA, TRKB, and TRKC (encoded by NTRK1, NTRK2, and NTRK3 genes, respectively) and their neurotrophin ligands regulate growth, differentiation and survival of neurons. Group: Biochemicals. Alternative Names: (3S) -N- [5- [ (2R) -2- (2, 5-Difluorophenyl) -1-pyrrolidinyl] pyrazolo [1, 5-a] pyrimidin-3-yl] -3-hydroxy-1-pyrrolidinecarboxamide ; ARRY 470; LOXO 101; Vitrakvi.; (S) -N- (5- ( (R) -2- (2, 5-difluorophenyl) pyrrolidin-1-yl) pyrazolo[1, 5-a]pyrimidin-3-yl) -3-hydroxypyrrolidine-1-carboxamide Sulfate. CAS No. 1223405-08-0. Pack Sizes: 10mg, 25mg, 50mg. Molecular Formula: C??H??F?N?O? H?O?S. US Biological Life Sciences. | Worldwide |
| PEPLEOMYCIN SULFATE | Peplomycin is a semisynthetic analog of Bleomycin. It is a mixture of several basic glycopeptide antineoplastic antibiotics that isolated from the fungus Streptomyces verticillus. Peplomycin can form complexes with iron that reduce molecular oxygen to superoxide and hydroxyl radicals. This leads to single- and double-stranded breaks in DNA. Peplomycin is a DNA synthesis inhibitor and has been used for the treatment of a various of Malignancies. Uses: Malignancies. Synonyms: N1- [3- [ [ (1S) -1-phenylethyl] amino] propyl] bleomycinamide Sulfate; NK 631; NSC-276382. Grades: 98%. CAS No. 70384-29-1. Molecular formula: C61H90N18O25S3. Mole weight: 1571.67. |  |
| Polymyxin B3 sulfate | It is produced by the strain of Pseudomonas sp. Polymyxin B3 sulfate is an individual fraction found in the antibiotic mixture polymyxin B sulfate. Polymyxin B targets and alters permeability lipopolysaccharide (LPS) of gram-negative bacteria leading to lysing of the cell. Grades: ≥90.0% by HPLC. Molecular formula: C55H96N16O13.xH2O4S. Mole weight: 1189.45 (free base). | |
| Polymyxin B6 sulfate | It is produced by the strain of Bacillus Polymyxa. Polymyxin B sulfate is a polypeptide antibiotic and is composed of polymyxins B1, B2, and B3 with fractions B1 and B2 comprising the majority of the mixture. Polymyxin B targets and alters permeability lipopolysaccharide (LPS) of gram-negative bacteria leading to lysing of the cell. Grades: >90.0%. Molecular formula: C56H98N16O14.xH2SO4. Mole weight: 1219.47 (free base). | |
| Polymyxin Ile-B1 Sulfate | It is produced by the strain of Pseudomonas Sp. It is one of the individual polypeptide components in polymyxin B sulfate. Polymyxin B targets and alters permeability lipopolysaccharide (LPS) of gram-negative bacteria leading to lysing of the cell. Synonyms: Polymyxin B1-I sulfate; Polymyxin II Sulfate; Polymyxin B1 Isoleucine sulfate. Grades: ≥90.0%. Molecular formula: C56H98N16O13.xH2O4S. Mole weight: 1203.47 (free base). | |
| Potassium Peroxymonosulfate Sulfate | Potassium Peroxymonosulfate Sulfate is an extremely potent oxidizer. It also may act as a bactericidal agent as treatment of bacterial spores with this agent leads to damage to the spores inner membrane. Plays a role in oxidative halogenation of various carbonyl and ketone compounds. Group: Biochemicals. Alternative Names: Potassium Peroxymonosulfate Sulfate (K5 (HSO5)2 (HSO4) (SO4)); Potassium Peroxymonosulfate Sulfate (K5[HSO3 (O2)]2 (HSO4) (SO4)); Basolan 2448; Caro Salt; Caroat; Caroate; Caro's Salt; Caro's Triple Salt; Curox; L-Gel; Oxone; PS 16; PS 16 (salt); Potassium Peroxymonosulfate Sulfate (2KHSO5.KHSO4.K2SO4); Potassium persulfate triple salt; Urutora San. Grades: Highly Purified. CAS No. 37222-66-5. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| Quinidine | Quinidine occurs in cinchona bark to about0.25-0.3% and also in cuprea bark. It is present in quinine sulfate mother liquor. Itis formed by isomerization of quinine. Itis used in the prevention of certain cardiacarrhythmias.Primary indications for the use of quinidine include (1) abolition of premature complexes that have an atrial, A-V junctional, or ventricular origin; (2) restoration of normal sinus rhythm in atrial flutter and atrial fibrillation after controlling the ventricular rate with digitalis; (3) maintenance of normal sinus rhythm after electrical conversion of atrial arrhythmias; (4) prophylaxis against arrhythmias associated with electrical countershock; (5) termination of ventricular tachycardia; and (6) suppression of repetitive tachycardia associated with Wolff- Parkinson-White (WPW) syndrome. Although quinidine often is successful in producing normal sinus rhythm, its administration in the presence of a rapid atrial rate (flutter and possibly atrial fibrillation) can lead to a further and dangerous increase in the ventricular rate secondary to inhibition of basal vagal tone upon the A-V node. For this reason, digitalis should be used before quinidine when one is attempting to convert atrial flutter or atrial fibrillation to normal sinus rhythm. Group: Heterocyclic organic compound. Alternative Names: (8R,9S)-6'-Methoxycinchonan-9-ol. CAS No. 56-54-2. Molecular formula: C20H24N2O2. Mole weight: 324.4. Appearanc | |
| Tetradecylphosphonic acid | 98%. Uses: Tdpa can be used to cap copper nanoparticles to protect them from oxidation. it may also be used in the synthesis of cadmium sulfate (cds) core, which can be used in the fabrication of cadmium selenium (cdse)/cds core quantum dots (qds). it may also be coated on caesium lead bromide (cspbbr3) perovskite quantum dots for the development of white light emitting diodes (wled). Group: Self-assembly materials self assembly and contact printing materials. Alternative Names: TPA, TDPA. CAS No. 4671-75-4. Pack Sizes: 1 g/5 g/100 g. Product ID: tetradecylphosphonic acid. Molecular formula: 278.37 g/mol. Mole weight: C14H31O3P. CCCCCCCCCCCCCCP(=O)(O)O. InChI=1S / C14H31O3P / c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18 (15, 16) 17 / h2-14H2, 1H3, (H2, 15, 16, 17). BVQJQTMSTANITJ-UHFFFAOYSA-N. | |
| Vinblastine sulfate | Vinblastine sulfate, also called cellblastin, derived from C. roseus, as a microtubule disrupter and antineoplastic agent, it binds tubulin and disrupts microtubule assembly and proper formation of the mitotic spindle, which leads to the assembly of microtubules and causing M phase-specific cell cycle arrest. Uses: Anticancer. Synonyms: cell pharm Brand of Vinblastine Sulfate; cellblastin; EG Labo Brand of Vinblastine Sulfate; Faulding Brand of Vinblastine Sulfate; Gastrozepin Brand of Vinblastine Sulfate; Gry Brand of Vinblastine Sulfate; Hexal Brand of Vinblastine Sulfate; Lemblastine; Lemery Brand of Vinblastine Sulfate; Lilly Brand of Vinblastine Sulfate; Sulfate, Vinblastine; Velban; Velbe; Vinblastin Hexal; Vinblastina Lilly; Vinblastine; Vinblastine Sulfate; Vinblastinsulfat-Gry; Vincaleukoblastine; Vinblastine sulfate; 143-67-9; C46H58N4O9H2SO4. Grades: >98%. CAS No. 143-67-9. Molecular formula: C46H58N4O9.H2SO4. Mole weight: 909.06. | |
| Gentamycin (Gentamicin) Sulfate USP | Broad spectrum, cell culture aminoglycoside antibiotic that is non toxic to viruses and mammalian cells at antibacterial levels. Inhibits growth of gram positive and negative bacteria, and mycoplasma. Inhibits normal protein synthesis by binding to L6 protein of 50S ribosomal subunit. Useful antibiotic for Baculovirus expression systems since mutations in rplF prevent Gentamycin from binding.Causes codon misreading by binding to the 30S ribosomal subunit, blocking the translocation of peptidyl-tRNA from the acceptor site to the donor site. Antibacterial against Gram-negative aerobic bacteria, Gram-positive bacteria and mycoplasmas. Used as a selection agent (gentamicin-resi...ption of the membrane. This increases the permeability of the cell envelope, leakage of cell contents, and leading to apoptosis and proteolysis (cell death). Causes also cell death by generation of free radicals, phospholipidosis, extracellular calcium-sensing recep- tor stimulation and energetic catastrophe. Source:Micromonospora sp. Group: Biochemicals. Alternative Names: Alcomici; Bristagen; Cidomycin; Duragentam; Garamycin; Garasol; Apogen, Gentiomycin C, Refobacin, NSC-82261; Gentamycin sulphate. Grades: Cell Culture Grade. CAS No. 1405-41-0. Pack Sizes: 5g, 25g, 100g, 500g, 1Kg. Molecular Formula: C21H43N5O7.H2SO4, Molecular Weight: ~575.6. US Biological Life Sciences. | Worldwide |
| Polymyxin B Sulfate USP (Bacillus polymyxa prazmowski migula, Aerosporin) | Antibiotic which inhibits PKC via bacterial membrane binding mechanism. Effective against gram negative bacteria. Polymyxins bind to the cell membrane and alter its structure making it more permeable. The resulting water uptake leads to cell death. They are cationic, basic proteins that act like detergents (surfactants}. Side effects include neurotoxicity and acute renal tubular necrosis. it is commonly used in the topical first aid preparation Neosporin. Polymyxin B belongs to a family of polypeptides with attached fatty acid, acting as a cationic detergent at physiological pH, both hydrophilic and hydrophobic properties. Polymyxin B is bactericidal for gram-negative, and has little to no effect on gram-positive since cell wall is too thick to permit access to membrane. Group: Biochemicals. Alternative Names: Bacillus polymyxa prazmowski migula, Aerosporin. Grades: Cell Culture Grade. CAS No. 1405-20-5. Pack Sizes: 10MU, 50MU, 100MU. US Biological Life Sciences. | Worldwide |
| Ristocetin A Sulfate (Ristocetin, Ristomycin III, Spontin, Riston) | Ristocetin A is a potent antibacterial glycopeptide antibiotic but was withdrawn for clinical use following a high incidence of thrombocytopenia. Further investigation found that ristocetin A induced platelet aggregation by binding to a factor absent in people suffering from von Willebrand's disease and lead to the use of ristocetin A as an important diagnostic aid. Source:Amycolatopsis sp. Group: Biochemicals. Alternative Names: Ristocetin; Ristomycin III; Spontin; Riston. Grades: Highly Purified. CAS No. 11140-99-1. Pack Sizes: 10mg, 25mg, 50mg. Molecular Formula: C95H110N8O44·H2SO4, Molecular Weight: 2166. US Biological Life Sciences. | Worldwide |
| Sulfatinib | Sulfatinib, also known as surufatinib, is an orally bioavailable, small molecule inhibitor of vascular endothelial growth factor receptors (VEGFR) 1, 2, and 3, and the fibroblast growth factor receptor type 1 (FGFR1), with potential antineoplastic and anti-angiogenic activities. Upon oral administration, sulfatinib binds to and inhibits VEGFRs and FGFR1 thereby inhibiting VEGFR- and FGFR1-mediated signal transduction pathways. This leads to a reduction of angiogenesis and tumor cell proliferation in VEGFR/FGFR1-overexpressing tumor cells. Expression of VEGFRs and FGFR1 may be upregulated in a variety of tumor cell types. Group: Inhibitors. Alternative Names: HMPL012; HMPL012; HMPL 012; Sulfatinib. CAS No. 1308672-74-3. Molecular formula: C24H28N6O3S. Mole weight: 480.59. Appearance: Solid powder. Purity: >98%. IUPACName: N-(2-(dimethylamino)ethyl)-1-(3-((4-((2-methyl-1H-indol-5-yl)oxy)pyrimidin-2-yl)amino)phenyl)methanesulfonamide. Canonical SMILES: CC1=CC2=C (N1)C=CC (OC3=NC (NC4=CC (CS (NCCN (C)C) (=O)=O)=CC=C4)=NC=C3)=C2. Catalog: ACM1308672743. | |
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