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| Product | Description | |
|---|---|---|
| Choline Iodide | 2-Hydroxy-N,N,N-trimethylethanaminium Iodide is used in the synthesis of a 5-cholinephosphate anti-HIV agent. Group: Biochemicals. Alternative Names: 2-Hydroxy-N,N,N-trimethylethanaminium Iodide; 2-Hydroxyethyltrimethyl Ammonium Iodide; Dilatol Zambon; Trimethyl(2-hydroxyethyl)ammonium Iodide. Grades: Highly Purified. CAS No. 17773-10-3. Pack Sizes: 25g, 50g, 100g. Molecular Formula: C?H??NO; I, Molecular Weight: 231.08. US Biological Life Sciences. |  Worldwide |
| Acetylcholine iodide | Acetylcholine iodide is a neurotransmitter found at neuromuscular junctions, autonomic ganglia, parasympathetic effector junctions, a subset of sympathetic effector junctions, and at many sites in the central nervous system. Uses: Cholinergic agonists. Synonyms: Acetylcolina; 2-acetyloxyethyl(trimethyl)azanium iodide. Grades: ≥95%. CAS No. 2260-50-6. Molecular formula: C7H16NO2·I. Mole weight: 273.11. |  |
| Acetylthiocholine iodide | Acetylthiocholine iodide can be used as a substrate for certain enzymes, such as cholinesterase, etc., and can be used to determine the activity level of these enzymes. In addition, the compound is used in some medical research, for example in the fields of neuroscience and organ physiology. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: S-Acetylthiocholine iodide; ATCh iodide. CAS No. 1866-15-5. Pack Sizes: 10 g. Product ID: HY-D0904. |  |
| Benzoyl choline iodide | Benzoyl choline iodide is an esteemed biomedicine renowned for its remarkable anticholinesterase activity. This unparalleled compound exerts its therapeutic prowess by indefatigably suppressing the action of acetylcholinesterase, culminating in a momentous elevation of acetylcholine levels and an amelioration of neurochemical transmission. CAS No. 17518-43-3. Molecular formula: C12H18INO2. Mole weight: 335.18. | |
| o,o-Succinyldicholine iodide | o,o-Succinyldicholine iodide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ascuron;bis(beta-dimethylaminoethyl)succinatebis(methyliodide);celocurin;celocurine;choline,iodide,succinate(2:1);curacit;diacetylcholinediiodide;diacetylcholineiodide. Product Category: Heterocyclic Organic Compound. CAS No. 541-19-5. Molecular formula: C14H31IN2O4. Mole weight: 544.201. Product ID: ACM541195. Alfa Chemistry ISO 9001:2015 Certified. Categories: Suxamethonium iodide. |  |
| Thiocholine iodide | Thiocholine iodide is an important hydrolyzed product of acetylthio-choline iodide and could be used and one of the substrates of Cholinesterase. Uses: For research used only. Synonyms: (2-Mercaptoethyl)trimethylammonium iodide (7CI); Ammonium, (2-mercaptoethyl)trimethyl-, iodide (8CI); Ethanaminium, 2-mercapto-N,N,N-trimethyl-, iodide (9CI); Cholinethiol iodide; Thiocholine iodide; TChI. Grades: ≥ 95.0 %. CAS No. 7161-73-1. Molecular formula: C5H14INS. Mole weight: 247.14. | |
| 4-DAMP | 4-DAMP is a potent and selective antagonist of the M3 cholinergic receptor. [3H]-4-DAMP selectively labels M1 and M3 receptors. Blockade of mAChR M2 leads to a decrease of blood pressure in dose manner in spotaneously hypertensive rats. Synonyms: 1,1-Dimethyl-4-diphenylacetoxypiperidinium iodide; 4-Damp methiodide; 4-Diphenylacetoxy-N-methylpiperidine methiodide; 4-DAMP iodide. Grades: ≥99% by HPLC. CAS No. 1952-15-4. Molecular formula: C21H26INO2. Mole weight: 451.33. | |
| Acetyl-ss-(methylthio)choline | Acetyl-ss-(methylthio)choline. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Acetyl-beta-(methylthio)choline, CID166487, 76721-90-9. Product Category: Heterocyclic Organic Compound. CAS No. 76721-90-9. Molecular formula: C8H18INO2S. Mole weight: 319.20349. Purity: 0.96. IUPACName: (2-acetyloxy-2-methylsulfanylethyl)-trimethylazanium iodide. Canonical SMILES: CC(=O)OC(C[N+](C)(C)C)SC. Product ID: ACM76721909. Alfa Chemistry ISO 9001:2015 Certified. Categories: SCHEMBL11084240. | |
| Ecothiophate iodide | Ecothiophate iodide is a potent, long-acting cholinesterase inhibitor. It covalently binds by its phosphate group to serine group at the active site of the cholinesterase. It binds irreversibly to cholinesterase. It is used as an ocular antihypertensive in the treatment of chronic glaucoma and accommodative esotropia in some cases. It is also an anticholinesterase drug and used as a miotic. It has been listed. Uses: Ecothiophate iodide is used as an ocular antihypertensive in the treatment of chronic glaucoma and accommodative esotropia in some cases. it is also an anticholinesterase drug and used as a miotic. Synonyms: 2-[ (Diethoxyphosphinyl) thio]ethanaminium iodide; Phospholine iodide; N- (2- (Diethoxyphosphinylthio) ethyl) trimethylammonium iodide; Ethanaminium, 2-((diethoxyphosphinyl)thio)-N,N,N-trimethyl-, iodide. Grades: 98%. CAS No. 513-10-0. Molecular formula: C9H23INO3PS. Mole weight: 383.23. | |
| Gallamine Triethiodide | Gallamine Triethiodide is a cholinergic receptor blocker with an IC50 of 68.0 ± 8.4 μM. It is is a non-depolarising muscle relaxant. Synonyms: Gallamine Triethiodide; Flaxedil; Tricuran; Gallamoni jodidum; Gallaminii iodidum; Triethyl Iodide, Gallamine; Iodide, Gallamine; Triethyl Iodide, Gallamonium; Gallamine Triethochloride. Grades: >98%. CAS No. 65-29-2. Molecular formula: C30H60I3N3O3. Mole weight: 891.53. | |
| NETA alpha (2- (alpha-Naphthoyl) ethyltrimethylammonium iodide) | Potent fluorescent inhibitor of choline acetyltransferase. Group: Biochemicals. Alternative Names: 2- (alpha-Naphthoyl) ethyltrimethylammonium iodide. Grades: Highly Purified. CAS No. 31059-54-8. Pack Sizes: 5mg, 25mg. US Biological Life Sciences. | Worldwide |
| Tetrabutylammonium Iodide | Tetrabutylammonium Iodide is one of numerous perovskite precursor materials. Uses: Tetrabutylammonium iodide is used in the preparation of novel quaternary amines to serve as antibacterial agents in the rise of drug-resistant bacteria,it is also used in phosphonium reversible inhibitors of cholinesterases. Group: Battery materials dye-sensitized solar cell (dssc) materials polymerization reagents. Alternative Names: TBAI, Tetrabutyl ammonium iodide, Tetra-n-butylammonium iodide, Tetrabutylazanium iodide, N,N,N-Tributyl-1-butanaminium iodide. CAS No. 311-28-4. Product ID: tetrabutylazanium; iodide. Molecular formula: 369.38. Mole weight: C16H36IN. CCCC[N+](CCCC)(CCCC)CCCC.[I-]. InChI=1S/C16H36N. HI/c1-5-9-13-17(14-10-6-2, 15-11-7-3)16-12-8-4; /h5-16H2, 1-4H3; 1H/q+1; /p-1. DPKBAXPHAYBPRL-UHFFFAOYSA-M. >98.0%T. |  |
| Tetra-n-butylammonium Iodide | Tetra-n-butylammonium Iodide is used in the preparation of novel quaternary amines to serve as antibacterial agents in the rise of drug-resistant bacteria. Also used in phosphonium reversible inhibitors of cholinesterases. Group: Biochemicals. Alternative Names: N,N,N-Tributyl-1-butanaminium Iodide (1:1); N,N,N-Tributyl-1-butanaminium Iodide; Tetrabutyl-Ammonium Iodide; Tetrabutylammonium Iodide; Tetra-n-butylammonium Iodide. Grades: Highly Purified. CAS No. 311-28-4. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| Trimethyl-[2-methyl-4-oxo-4-[2-(trimethylazaniumyl)ethoxy]butan-2-yl]azanium diiodide | Trimethyl-[2-methyl-4-oxo-4-[2-(trimethylazaniumyl)ethoxy]butan-2-yl]azanium diiodide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: NIOSH/EJ4171800, CID60273, LS-17026, LS-45611, EJ4171800, (2-Carboxy-1,1-dimethylethyl)trimethylammonium iodide ester with choline iodide, 2-Trimethylammonioethyl 3-methyl-3-trimethylammoniobutyrate diiodide, Ammonium, (2-carboxy-1,1-dimethylethyl)trimethyl-, iodide, ester with choline iodide, 2-Butanaminium, 4-oxo-N,N,N,2-tetramethyl-4-(2-(trimethylammonio)ethoxy)-, diiodide, 4-Oxo-N,N,N,2-tetramethyl-4-(2-(trimethylammonio)ethoxy)-2-butanaminium diiodide, 108903-57-7. Product Category: Heterocyclic Organic Compound. CAS No. 108903-57-7. Molecular formula: C13H30I2N2O2. Mole weight: 500.198 g/mol. Purity: 0.96. IUPACName: trimethyl-[2-methyl-4-oxo-4-[2-(trimethylazaniumyl)ethoxy]butan-2-yl]azanium diiodide. Canonical SMILES: CC(C)(CC(=O)OCC[N+](C)(C)C)[N+](C)(C)C.[I-].[I-]. Product ID: ACM108903577. Alfa Chemistry ISO 9001:2015 Certified. | |
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