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| Product | Description | |
|---|---|---|
| Lead Chloride | Lead Chloride is generally immediately available in most volumes. Group: Glass additives. Alternative Names: Plumbous chloride. CAS No. 7758-95-4. Product ID: Dichlorolead. Molecular formula: 278. Mole weight: PbCl2. Cl[Pb]Cl. InChI=1S/2ClH.Pb/h2*1H;/q;+2/p-2. HWSZZLVAJGOAAY-UHFFFAOYSA-L. 99%+. |  |
| Lead Chloride 99+% | Lead Chloride 99+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 7758-95-4. Pack Sizes: 100g, 1Kg, 2.5Kg. US Biological Life Sciences. |  Worldwide |
| Lead chloride oxide | Heterocyclic Organic Compound. Alternative Names: Lead chloride oxide, EINECS 235-383-5, 12205-72-0. CAS No. 12205-72-0. Molecular formula: Cl2O7Pb8. Mole weight: 1840.501800 [g/mol]. Purity: 0.96. IUPACName: lead(2+); oxygen(2-); dichloride. Catalog: ACM12205720. |  |
| CH3NH3PbICl2(MAPbICl2 )Methylammonium Lead Chloride Iodide, >99% | CH3NH3PbICl2(MAPbICl2 )Methylammonium Lead Chloride Iodide, >99%. Group: other glass and ceramic materials. CAS No. 1472068-56-6. | |
| Lead (II) Chloride | LEAD (II) CHLORIDE, 99.5% pure, -20 mesh, (Synonym: Lead Dichloride), Formula: PbCl2. CAS No. 7758-95-4. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Lead (II) Chloride | Lead (II) Chloride. Grades: 99.99% Extremely High (>=99%). CAS No. 7758-95-4. Pack Sizes: Gram Quantities: 25 gm , 100 gm. Order Number: 2222. |  www.prochemonline.com |
| Lead (II) Chloride | Lead (II) Chloride. Grades: 99.9% Extremely High (>=99%). CAS No. 7758-95-4. Pack Sizes: Gram Quantities: 25 gm, 100 gm. Order Number: 2221. | www.prochemonline.com |
| Lead (II) Chloride | Lead (II) Chloride. Grades: 99.% Extremely High (>=99%). CAS No. 7758-95-4. Pack Sizes: Gram Quantities: 500 gm , 2 kg. Order Number: 2218. | www.prochemonline.com |
| Lead(II) Chloride | Powder , 98%. Uses: Reagents for organic-inorganic perovskite: lead chloride. Group: Electrolytesperovskite materials. Alternative Names: Cotunnite. CAS No. 7758-95-4. Pack Sizes: 5 g/250 g/1 kg. Product ID: dichlorolead. Molecular formula: 278.10 g/mol. Mole weight: PbCl2;Cl2Pb. Cl[Pb]Cl. InChI=1S/2ClH.Pb/h2*1H;/q;;+2/p-2. HWSZZLVAJGOAAY-UHFFFAOYSA-L. | |
| Lead(II) Chloride | Powder , 98%. Uses: Reagents for organic-inorganic perovskite: lead chloride. Group: Organic lead. Alternative Names: Cotunnite. CAS No. 7758-95-4. Molecular formula: PbCl2;Cl2Pb. Mole weight: 278.10 g/mol. IUPACName: dichlorolead. Canonical SMILES: Cl[Pb]Cl. Density: 5.85 g/mL at 25 °C (lit.). ECNumber: 231-845-5. Catalog: ACM7758954-6. | |
| Lead(II) Chloride [for Perovskite precursor] | Lead chloride appears as a white solid.;DryPowder. Group: Perovskite solar cell (psc) materials. CAS No. 7758-95-4. Product ID: dichlorolead. Molecular formula: 278g/mol. Mole weight: PbCl2;Cl2Pb. Cl[Pb]Cl. InChI=1S/2ClH.Pb/h2*1H;/q;;+2/p-2. HWSZZLVAJGOAAY-UHFFFAOYSA-L. | |
| Lead(II) Chloride (purified by sublimation) [for Perovskite precursor] | Lead chloride appears as a white solid.;DryPowder. Group: other material building blocksperovskite solar cell (psc) materials. CAS No. 7758-95-4. Product ID: dichlorolead. Molecular formula: 278g/mol. Mole weight: PbCl2;Cl2Pb. Cl[Pb]Cl. InChI=1S/2ClH.Pb/h2*1H;/q;;+2/p-2. HWSZZLVAJGOAAY-UHFFFAOYSA-L. | |
| Methylammonium lead Chloride Iodide, >99% | Methylammonium lead Chloride Iodide, >99%. Group: other glass and ceramic materials. CAS No. 1446121-07-8. | |
| 1,3-Bis(2,6-Diisopropylphenyl)-4,5-Dihydroimidazolium Tetrafluoroborate | In-situ deprotonation leads to metal carbene species which acts as a catalyst in a variety of C-C and C-N bond forming reactions. Ligand used in the nickel or palladium-catalyzed coupling of aryl chlorides and amines. Ligand used for the palladium-catalyzed arylation of esters and amides. Ligand used for the palladium-catalyzed intermolecular amination of Csp3-H Bonds. Ligand used for the nickel-catalyzed hydrogenation of olefins. Group: Organic phosphine compounds. Alternative Names: 1,3-Bis(2,6-Diisopropylphenyl)-4,5-Dihydro-1H-Imidazol-3-Ium Tetrafluoroborate. CAS No. 282109-83-5. Molecular formula: C27H39BF4N2. Mole weight: 478.4. Appearance: White powder. Purity: 0.98. IUPACName: 1,3-bis[2,6-di(propan-2-yl)phenyl]-4,5-dihydroimidazol-1-ium;tetrafluoroborate. Canonical SMILES: [B-] (F) (F) (F)F. CC (C)C1=C (C (=CC=C1)C (C)C)N2CC[N+] (=C2)C3=C (C=CC=C3C (C)C)C (C)C. Catalog: ACM282109835-1. | |
| 2-Chloro-5-bromopyridine | The simple LiCl-?mediated insertion of magnesium into aryl chlorides and bromides at moderate temps. leads to functionalized organomagnesium reagents. Group: Biochemicals. Grades: Highly Purified. CAS No. 53939-30-3. Pack Sizes: 1g, 5g. Molecular Formula: C5H3BrClN, Molecular Weight: 192.44. US Biological Life Sciences. | Worldwide |
| 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 |
| adenosyl-chloride synthase | This enzyme, isolated from the marine bacterium Salinispora tropica, catalyses an early step in the pathway leading to biosynthesis of the proteosome inhibitor salinosporamide A. The enzyme is very similar to EC 2.5.1.63, adenosyl-fluoride synthase, but does not accept fluoride. Group: Enzymes. Synonyms: chlorinase; 5'-chloro-5'-deoxyadenosine synthase. Enzyme Commission Number: EC 2.5.1.94. 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-2833; adenosyl-chloride synthase; EC 2.5.1.94; chlorinase; 5'-chloro-5'-deoxyadenosine synthase. Cat No: EXWM-2833. |  |
| Benzodiazepine (BSA) | The term benzodiazepine refers to the portion of the structure composed of a benzene ring fused to a seven membered diazepine ring. Benzodiazepine is a central nervous system depressants, a sedative hypnotic agent. Benzodiazepine receptors are located on the alpha subunit of the GABA receptor located almost exclusively on postsynaptic nerve endings in the CNS (especially cerebral cortex). Benzodiazepines enhance the GABA transmitter in the opening of postsynaptic chloride channels which leads to hyperpolarization of cell membranes. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Benzodiazepine (BZO) (BGG) | The term benzodiazepine refers to the portion of the structure composed of a benzene ring fused to a seven membered diazepine ring. Benzodiazepine is a central nervous system depressants, a sedative hypnotic agent. Benzodiazepine receptors are located on the alpha subunit of the GABA receptor located almost exclusively on postsynaptic nerve endings in the CNS (especially cerebral cortex). Benzodiazepines enhance the GABA transmitter in the opening of postsynaptic chloride channels which leads to hyperpolarization of cell membranes. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Benzodiazepine (BZO) (BSA) | The term benzodiazepine refers to the portion of the structure composed of a benzene ring fused to a seven membered diazepine ring. Benzodiazepine is a central nervous system depressants, a sedative hypnotic agent. Benzodiazepine receptors are located on the alpha subunit of the GABA receptor located almost exclusively on postsynaptic nerve endings in the CNS (especially cerebral cortex). Benzodiazepines enhance the GABA transmitter in the opening of postsynaptic chloride channels which leads to hyperpolarization of cell membranes. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Benzodiazepine (Oxazepam) (BSA) | The term benzodiazepine refers to the portion of the structure composed of a benzene ring fused to a seven membered diazepine ring. Benzodiazepine is a central nervous system depressants, a sedative hypnotic agent. Benzodiazepine receptors are located on the alpha subunit of the GABA receptor located almost exclusively on postsynaptic nerve endings in the CNS (especially cerebral cortex). Benzodiazepines enhance the GABA transmitter in the opening of postsynaptic chloride channels which leads to hyperpolarization of cell membranes. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cetalkonium chloride | Cetalkonium chloride is an ammonium antiseptic agent used in many topical agents for infections of mouth, throat and eye. Cetalkonium chloride acts as anti-inflammatory amphiphilic agent. Cetalkonium chloride is a cationic surfactant, that improves the precorneal residence time and bioavailability of drugs. Cetalkonium chloride interacts with the negative charges on the bacterial cell membrane, disrupts the integrity of the cell membrane, causes leakage of cell contents and ultimately leading to bacterial death [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Benzyldimethylhexadecylammonium chloride. CAS No. 122-18-9. Pack Sizes: 10 mM * 1 mL; 1 g. Product ID: HY-B1597. |  |
| Doramectin | Doramectin is a biosynthetic avermectin derived from a mutant of the original Streptomyces avermitilis strain supplemented with a cyclohexylcaboxylic acid starting unit. Doramectin was developed as an anthelmintic for internal parasite control. The presence of the cyclohexyl group replacing the sec-butyl moiety affords greater hydrophobicity and longer biological half-life compared to avermectin. Like the other milbemycin / avermectins, it selectively binds to parasite glutamate-gated chloride ion channels and disrupts neurotransmission leading to paralysis and death of the parasite. Group: Biochemicals. Grades: Highly Purified. CAS No. 117704-25-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Doramectin (25-Cyclohexyl-5-O-demethyl-25-de (1-methylpropyl) avermectin A1A,. 25-Cylohexyl-avermectin B1, UK-67994, Dectomax) | Doramectin is a biosynthetic avermectin derived from a mutant of the original Streptomyces avermitilis strain supplemented with a cyclohexylcaboxylic acid starting unit. Doramectin was developed as an anthelmintic for internal parasite control. The presence of the cyclohexyl group replacing the sec-butyl moiety affords greater hydrophobicity and longer biological half-life compared to avermectin. Like the other milbemycin / avermectins, it selectively binds to parasite glutamate-gated chloride ion channels and disrupts neurotransmission leading to paralysis and death of the parasite. Group: Biochemicals. Alternative Names: 25-Cyclohexyl-5-O-demethyl-25-de (1-methylpropyl) avermectin A1A; 25-Cylohexyl-avermectin B1; UK-67994; Dectomax. Grades: Highly Purified. CAS No. 117704-25-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Jatrorrhizine hydrochloride | Jatrorrhizine hydrochloride is a naturally occurring compound, which has been shown to have hypoglycemic effects and can be used for the treatment of skin cancer. It is an analogue of berberine that inhibits mitochondrial membrane potential, leading to cell death by inhibiting energy metabolism and causing chromatographic analysis. Jatrorrhizine hydrochloride also inhibits the synthesis of proteins required for glycolysis, including hexokinase 2 (HK2), phosphofructokinase 1 (PFK1), and pyruvate kinase M2 (PKM2). This drug is metabolized by esterases or glucuronidases to form benzalkonium chloride or ginsenoside RG3. This active form binds to penicillin-binding protein, which may lead to metabolic disorders such as hepatic steatosis. Group: Other alkaloids. CAS No. 2106804-01-5. Molecular formula: C20H20NO4·HCl. Mole weight: 374.84 g/mol. Canonical SMILES: COC1=C (C2=C[N+]3=C (C=C2C=C1)C4=CC (=C (C=C4CC3)O)OC)OC. [Cl-]. Catalog: ACM2106804015. | |
| Lumacaftor | Lumacaftor is the second investigational oral candidate compound for the treatment of cystic fibrosis (CF). Lumacaftor may act to restore the function of the cystic fibrosis transmembrane conductance regulator (CFTR) protein, the defective cell membrane protein responsible for the progression of CF. Lumacaftor defects in the CFTR protein affect the transport of chloride and other ions across cells, and lead to the accumulation of thick, sticky mucus in the lungs of patients with CF. This mucus fosters chronic infection and inflammation, and results in irreversible lung damage. Synonyms: VX-809; VX809; VX 809; VRT 826809; VRT826809; VRT-826809. Grades: ≥98%. CAS No. 936727-05-8. Molecular formula: C24H18F2N2O5. Mole weight: 452.41. |  |
| Milbemycin oxime | Milbemycin oxime is a semi-synthetic macrolide. As a nematocide and insecticide in veterinary medicine, it opens glutamate sensitive chloride channels in neurons of invertebrates that leads to paralysis by hyperpolarisation of these cells and signal transfer blocking. M1-family aminopeptidase: IC50=2.6 μM (Plasmodium falciparum 3D7); Bile acid transporter: IC50=3.6 μM (human); TGR5: IC50=36.4 μM (human); HCT-116: IC50 >50 μM (human); GBM: IC50 >50 μM (human). Uses: A broad spectrum insecticide; used for treatment and prevention of heartworm in dogs and cats. Synonyms: Milbemycin A 5-oxime; Milbemite; Trifexis; Interceptor; Milbe Mite. Grades: ≥98%. CAS No. 129496-10-2. Molecular formula: C126H176N4O28. Mole weight: 2194.78. | |
| Milbemycin Oxime | Milbemycin oxime is a semi-synthetic macrocyclic lactone prepared by the oxidation and oximation of a mixture of two natural products, milbemycin A3 and A4 (in ~70: 30 ratio). Moxidectin oxime, marketed as Interceptor, is used therapeutically for the prevention of intestinal parasites in dogs. Like the other milbemycin / avermectins, it was developed for intestinal parasite control in animals and acts by opening glutamate sensitive chloride channels in neurons of invertebrates leading to paralysis by hyperpolarisation of these cells and signal transfer blocking. Group: Biochemicals. Grades: Highly Purified. CAS No. 129496-10-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Native Bovine Cathepsin C | Cathespin C is a dipeptidyl aminopeptidase that can sequentially remove dipeptides from a peptide chain with an unsubstituted N-terminus. The enzyme exhibits a preference for glycine and proline as N-terminal aminoacids. Substrates that have an N-terminal lysyl or arginyl residue, or a penultimate proryl residue are not targeted by this enzyme. The endopeptidase activity requires the presence of halide ions and sulfydryl activators. Applications: Cathepsin c has been used in a study that demonstrated the potential of a proteomics approach to identify novel proteins expressed by extravillous trophoblast and to uncover the mechanisms leading to disease states in pregnancy. catheps...s. Synonyms: CTSC; cathepsin C; 9032-68-2; EC 3.4.14.1; dipeptidyl aminopeptidase I; dipeptidyl transferase; dipeptidyl transferase; dipeptide arylamidase I; DAP I; dipeptidyl-peptidase I; DPP-I; CPPI; DPP1; DPPI; HMS; JP; JPD; PALS; PDON1; PLS. Enzyme Commission Number: EC 3.4.14.1. CAS No. 9032-68-2. CTSC. Activity: > 5 units/mg protein. Form: Lyophilized from a 1 M sodium chloride solution. Source: Bovine spleen. Species: Bovine. CTSC; cathepsin C; 9032-68-2; EC 3.4.14.1; dipeptidyl aminopeptidase I; dipeptidyl transferase; dipeptidyl transferase; dipeptide arylamidase I; DAP I; dipeptidyl-peptidase I; DPP-I; CPPI; DPP1; DPPI; HMS; JP; JPD; PALS; PDON1; PLS. Cat No: NATE-0170. | |
| Nitidine chloride | Nitidine chloride, a potential anti-malarial lead compound derived from Zanthoxylum nitidum (Roxb) DC, exerts potent anticancer activity through diverse pathways, including inducing apoptosis , inhibiting STAT3 signaling cascade, DNA topoisomerase 1 and 2A , ERK and c-Src/FAK associated signaling pathway, also has anti-inflammatory activity. Nitidine chloride inhibits LPS-induced inflammatory cytokines production via MAPK and NF-kB pathway [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 13063-04-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N0498. | |
| Nitidine chloride | Nitidine chloride is a potent inducer of energy metabolism and has been shown to stimulate the growth of cells in tissue culture. It is also active against cancer cells, and has been shown to decrease cell proliferation, induce apoptosis, and inhibit angiogenesis. Nitidine chloride has been shown to be an inhibitor of protein synthesis by binding to the polymerase chain reaction (PCR) enzyme. Nitidine chloride can also affect cell nuclei by inhibiting DNA replication. The mechanism of action for nitidine chloride is not fully understood but may be due to its ability to bind with DNA or RNA in cells. This binding inhibits transcription and translation processes, leading to inhibition of protein synthesis and cell death. Nitidine chloride is found naturally in plants such as Ginkgo biloba and Acorus calamus. The compound can be synthesized from chloroacetamide, a natural compound that is produced by bacteria such as Corynebacterium glutamicum. Group: Other alkaloids. CAS No. 13063-04-2. Molecular formula: C21H18ClNO4. Mole weight: 383.82 g/mol. Canonical SMILES: C[N+]1=CC2=CC (=C (C=C2C3=C1C4=CC5=C (C=C4C=C3)OCO5)OC)OC. [Cl-]. Catalog: ACM13063042. | |
| Thiamine-d3 Hydrochloride | Labeled Thiamine. Essential nutrient required for carbohydrate metabolism; also involved in nerve function. Biosynthesized by microorganisms and plants. Dietary sources include whole grains, meat products, vegetables, milk, legumes and fruit. Also present in rice husks and yeast. Converted in vivo to Thiamine diphosphate, a coenzyme in the decarboxylation of α-keto acids. Chronic deficiency may lead to neurological impairment, bariberi, Wernicke-Korsakoff syndrome. Group: Biochemicals. Alternative Names: 3-[(4-Amino-2-(methyl-d3)-5-pyrimidinyl)methyl]-5-(2-hydroxyethyl)-4-methyl-chloridethiazolium. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Thiamine Hydrochloride (Vitamin B1, Aneurine) | Thiamine is a essential nutrient required for carbohydrate metabolism; also involved in nerve function. Biosynthesized by microorganisms and plants. Dietary sources include whole grains, meat products, vegetables, milk, legumes and fruit. Also present in rice husks and yeast. Converted in vivo to Thiamine diphosphate, a coenzyme in the decarboxylation of α-keto acids. Chronic deficiency may lead to neurological impairment, bariberi, Wernicke-Korsakoff syndrome. Group: Biochemicals. Alternative Names: 3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-5-(2-hydroxyethyl)-4-methyl-chloridethiazolium Hydrochloride; Aneurine Hydrochloride; Apate Drops; Beatine; Bedome; Begiolan; Benerva; Eskapen; Eskaphen; Thiamin Dichloride; Vinothiam; Vitamin B1 Hydrochloride; Vitaneuron. Grades: Cell Culture Grade. CAS No. 67-03-8. Pack Sizes: 100g, 500g, 1Kg. Molecular Formula: C12H17CIN4OS HCl, Molecular Weight: 337.3. US Biological Life Sciences. | Worldwide |
| Thiamine Hydrochloride (Vitamin B1, Aneurine) 99+% USP | Thiamine is a essential nutrient required for carbohydrate metabolism; also involved in nerve function. Biosynthesized by microorganisms and plants. Dietary sources include whole grains, meat products, vegetables, milk, legumes and fruit. Also present in rice husks and yeast. Converted in vivo to Thiamine diphosphate, a coenzyme in the decarboxylation of α-keto acids. Chronic deficiency may lead to neurological impairment, bariberi, Wernicke-Korsakoff syndrome. Group: Biochemicals. Alternative Names: 3-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]-5-(2-hydroxyethyl)-4-methyl-chloridethiazolium Hydrochloride; Aneurine Hydrochloride; Apate Drops; Beatine; Bedome; Begiolan; Benerva; Eskapen; Eskaphen; Thiamin Dichloride; Vinothiam; Vitamin B1 Hydrochloride; Vitaneuron. Grades: USP. CAS No. 67-03-8. Pack Sizes: 250g, 1Kg, 5Kg. Molecular Formula: C12H17CIN4OS HCl, Molecular Weight: 337.3. US Biological Life Sciences. | Worldwide |
| Veratrine HCl | Veratrine HCl is a vasoactive intestinal peptide that binds to ganglia and produces whole-body effects. It is an inhibitor of chloride channels, which leads to increased acetylcholine release. Veratrine HCl is a potent competitive antagonist of acetylcholine at muscarinic receptors in the heart and brain, leading to decreased cardiac and serotonin activity. The drug also has a depressant effect on the central nervous system. Veratrine HCl increases the amount of chloride in the blood and expiratory flow by inhibiting choline uptake into cells. It is used as an analytical method for measuring triazine herbicides. Group: Other alkaloids. Alternative Names: N-[(Benzyloxy)Carbonyl]-L-Tyrosyl-L-Valyl-N-[(3S)-5-Fluoro-1-Methoxy-1,4-Dioxo-3-Pentanyl]-L-alaninamide. CAS No. 17666-25-0. Molecular formula: C32H50ClNO9. Mole weight: 628.19 g/mol. Canonical SMILES: C/C=C (/C)\C (=O)O[C@H]1CC[C@]2 ([C@H]3[C@@]1 (O[C@@]24C[C@]5 ([C@@H]6CN7C[C@H] (CC[C@H]7[C@@] ([C@]6 ([C@H] (C[C@]5 ([C@@H]4CC3)O)O)O) (C)O)C)O)O)C. Cl. Catalog: ACM17666250. | |
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