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| Product | Description | |
|---|---|---|
| Alcohols, C6-12, ethoxylated propoxylated | Hair conditioning; Hair Fixing. Group: Non-ionic surfactants. Alternative Names: Alkyl-(C6-C12)-alcohol, ethoxylated & propoxylated. CAS No. 68937-66-6. Molecular formula: C17H38O2. Mole weight: 274.48. IUPACName: 1-Ethoxyhexane;1-propoxyhexane. Canonical SMILES: CCCCCCOCC.CCCCCCOCCC. Catalog: ACM68937666. |  |
| 1,1'-Oxydi-2-propanol | Alcohols. Alternative Names: 2,2'-Dihydroxyisopropyl ether. CAS No. 110-98-5. Molecular formula: C6H14O3. Mole weight: 134.17. Purity: 95%+. IUPACName: 1-(2-Hydroxypropoxy)propan-2-ol. Canonical SMILES: CC(COCC(C)O)O. Density: 1.02 g/mL at 25 °C(lit.). Catalog: ACM110985. | |
| 1,2-Benzenedimethanol | 1,2-Benzenedimethanol. Uses: This product is suitable for scientific research. Group: Monomers. Alternative Names: 1,2-Bis(hydroxymethyl)benzene, o-Xylene-α,α'-diol, Phthalyl alcohol. CAS No. 612-14-6. Product ID: [2-(hydroxymethyl)phenyl]methanol. Molecular formula: 138.16. Mole weight: C6H4(CH2OH)2. OCc1ccccc1CO. 1S/C8H10O2/c9-5-7-3-1-2-4-8 (7)6-10/h1-4, 9-10H, 5-6H2. XMUZQOKACOLCSS-UHFFFAOYSA-N. |  |
| 1,4-Cyclohexadiene Monoepoxide | 1,4-Cyclohexadiene Monoepoxide is a synthetic intermediate. It is used as a reactant in the enantioselective formal synthesis of 4-demethoxydaunomycin. Also used in the asymmetric synthesis of β-amino and vicinal amino alcohols. Group: Biochemicals. Grades: Highly Purified. CAS No. 6253-27-6. Pack Sizes: 50mg, 250mg. Molecular Formula: C6H8O. US Biological Life Sciences. |  Worldwide |
| 1-Amino-1-cyclopentanemethanol | Amino Alcohols. CAS No. 10316-79-7. Molecular formula: C6H13NO. Mole weight: 115.17. Catalog: ACM10316797. | |
| 1- (Hydroxy methyl ) cyclopropane acetonitrile | 1- (Hydroxy methyl ) cyclopropane acetonitrile is a reactant used in the preparation of benzothiazoles and thiazoles substituted benzyl alcohols as potent LTD4 antagonists. Group: Biochemicals. Grades: Highly Purified. CAS No. 152922-71-9. Pack Sizes: 250mg, 1g. Molecular Formula: C6H9NO, Molecular Weight: 111.14. US Biological Life Sciences. | Worldwide |
| (1'R,2'R,3aS,3"aS,8aR,8"aR)-(+)-3,3",3a,3"a,8,8",8a,8"a-Octahydrodispiro{2H-indeno[1,2-d]oxazole-2,1'-cyclohexane-2',2"-[2H]indeno[1,2-d]oxazole} WOLF BISOXAZOLIDINE | Catalyst used in the asymmetric addition of diethylzinc to aldehydes - synthesis of chiral alcohols. Catalysts used in the asymmetric addition of acetylenes and silylacetylenes to aldehydes. Catalyst used in the asymmetric addition of nitromethane to aldehydes - synthesis of β-hydroxynitromethanes. Group: Heterocyclic organic compound. Alternative Names: WOLF Bisoxazolidine;MFCD11973793;(1'R, 2'R, 3aS, 3"aS, 8aR, 8"aR)-(+)-3, 3".3a, 3"a, 8, 8", 8a, 8"a-Octahydrodispiro{2H-indeno[1, 2-d]oxazole-2, 1'-cyclohexane-2', 2"-[2H]indeno[1, 2-d]oxazole};947515-50-6. CAS No. 947515-50-6. Molecular formula: C24H26N2O2. Mole weight: 374.484g/mol. Canonical SMILES: C1CCC2 (C3 (C1)NC4C (O3)CC5=CC=CC=C45)NC6C (O2)CC7=CC=CC=C67. Catalog: ACM947515506. | |
| 2-(1,1-Dimethylethoxy)ethanol | 2- (1, 1-Dimethylethoxy) ethanol. Group: Biochemicals. Alternative Names: 2- (1, 1-Dimethylethoxy) ethanol; 2-tert-Butoxyethanol; 2-tert-Butoxyethyl Alcohol; Ethylene Glycol Mono-tert-butyl Ether; Ethylene Glycol tert-Butyl Ether; Swasolve ETB; tert-Butyl 2-Hydroxyethyl Ether; tert-Butyl Cellosolve. Grades: Highly Purified. CAS No. 7580-85-0. Pack Sizes: 10g. Molecular Formula: C6H14O2, Molecular Weight: 118.17. US Biological Life Sciences. | Worldwide |
| 2,2'-Bis(diphenylphosphino)biphenyl | Supporting ligand in a chiral diamine-ruthenium system for the enantioselective hydrogenation of ketones. Useful ligand for palladium-catalyzed amination and Kumada cross-coupling reactions Useful ligand for palladium-catalyzed synthesis of butatrenes. Useful ligand for iridium-catalyzed C-C cross-coupling of allenes with primary alcohols via transfer hydrogenation. Useful ligand for iridium-catalyzed C-C cross-coupling of dienes with primary alcohols via transfer hydrogenation. Useful ligand for iridium-catalyzed C-C cross-coupling of allylic gem-dicarboxylates with aldehydes via transfer hydrogenation. Useful ligand for the palladium-catalyzed synthesis of chiral allenylsilanes. Ruthenium-catalyzed synthesis of indoles. Ruthenium-catalyzed oxidative cyclization. Rhodium-catalyzed boron arylation. Group: Organic phosphine compounds. Alternative Names: BIPHEP; MFCD03094574; AKOS015911364; DB-009479; 1, 1'-[[1, 1'-BIPHENYL]-2, 2'-DIYL]BIS[1, 1-DIPHENYL]-PHOSPHINE; CTK3J1519; SCHEMBL1120987; 2,2'-Bis(diphenylphosphino)biphenyl; 2,2'-bis(diphenylphosphanyl)-1,1'-biphenyl; FT-0657577. CAS No. 84783-64-2. Molecular formula: C36H28P2. Mole weight: 522.568g/mol. IUPACName: [2- (2-diphenylphosphanylphenyl) phenyl]-diphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3C4=CC=CC=C4P (C5=CC=CC=C5)C6=CC=CC=C6. Catalog: ACM84783642. | |
| 2-Aminophenol | 2-Aminophenol. Group: Biochemicals. Alternative Names: (2-Hydroxyphenyl)amine; 1-Amino-2-hydroxybenzene; 1-Hydroxy-2-aminobenzene; 2-Amino-1-hydroxybenzene; 2-Aminophenol; 2-Aminophenyl Alcohol; 2-Hydroxyaniline; 2-Hydroxybenzenamine; BASF Ursol 3GA; Benzofur GG; C.I. 76520; C.I. Oxidation Base 17; Fouramine OP; NSC 1534; NSC 226261; Nako Yellow 3GA; Paradone Olive Green B; Pelagol 3GA; Pelagol Grey GG; Rodol 2G; Zoba 3GA; o-Aminohydroxybenzene; o-Aminophenol; o-Hydroxyaniline; o-Hydroxyphenylamine. Grades: Highly Purified. CAS No. 95-55-6. Pack Sizes: 10g. Molecular Formula: C6H7NO, Molecular Weight: 109.13. US Biological Life Sciences. | Worldwide |
| 2-Bromoacetic acid ethyl ester | Heterocyclic Organic Compound. Alternative Names: 2-Methylpentan-1-ol; 2-Methylamyl Alcohol; 2-METHYL-1-PENTANOL; 2-Propylpropanol. CAS No. 105-30-2. Molecular formula: C6H14O. Mole weight: 102.175. Appearance: clear colourless liquid. Purity: 0.96. IUPACName: 2-Methyl-1-pentanol. Density: 0.824 g/mL at 25ºC(lit.). Catalog: ACM105302. | |
| 2-Ethyl-1-butanol | 2-Ethyl-1-butanol. Group: Biochemicals. Alternative Names: 2-Ethylbutyl Alcohol; 3-Methylolpentane; NSC 8858; Pseudohexyl Alcohol. Grades: Highly Purified. CAS No. 97-95-0. Pack Sizes: 10ml. Molecular Formula: C6H14O, Molecular Weight: 102.17. US Biological Life Sciences. | Worldwide |
| 2-Furylmethanol | Furfuryl alcohol appears as a clear colorless liquid. Flash point 167°F. Boiling point 171°F. Denser than water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion and skin contact and moderately toxic by inhalation.; Liquid; Liquid; Liquid; Liquid; COLOURLESS LIQUID WITH CHARACTERISTIC ODOUR. TURNS RED OR BROWN ON EXPOSURE TO LIGHT AND AIR.;Colourless or pale yellowish liquid, mild, warm oily, "burnt" odour;Colorless to amber liquid with a faint, burning odor.;Colorless to amber liquid with a faint, burning odor. [Note: Darkens on exposure to light.]. Group: Polymers. CAS No. 25212-86-6. Product ID: furan-2-ylmethanol. Molecular formula: 98.1g/mol. Mole weight: C5H6O2;C5H6O2. C1=COC(=C1)CO. InChI=1S / C5H6O2 / c6-4-5-2-1-3-7-5 / h1-3, 6H, 4H2. XPFVYQJUAUNWIW-UHFFFAOYSA-N. | |
| 2-Hexyn-1-ol | 2-Hexyn-1-ol is a propargyl alcohol that is naturally found as a volatile fragrance component of chestnut blossoms. 2-Hexyn-1-ol also has potential antifungal properties against Aspergillus oryzae, a fungus that is used to produce fermented foods and beverages in Japan. Group: Biochemicals. Grades: Highly Purified. CAS No. 764-60-3. Pack Sizes: 2.5g, 10g. Molecular Formula: C6H10O, Molecular Weight: 98.14. US Biological Life Sciences. | Worldwide |
| 2-Methyl-2-pentanol | 2-Methyl-2-pentanol is a perfluorinated tertiary alcohol that is commonly found in fruits when they reach their maturation stages. Group: Biochemicals. Grades: Highly Purified. CAS No. 590-36-3. Pack Sizes: 2.5g, 10 g. Molecular Formula: C6H14O, Molecular Weight: 102.17. US Biological Life Sciences. | Worldwide |
| 2-Phenoxyethyl-1,1,2,2-d4 Alcohol | 2-Phenoxyethyl-1,1,2,2-d4 Alcohol. Alternative Names: Ethylene Glycol Monophenyl Ether. CAS No. 1219804-65-5. Molecular formula: C6H5OCD2CD2OH. Mole weight: 142.19. Purity: 98 atom % D. Catalog: ACM1219804655. | |
| 3-Pyridinemethanol | 3-Pyridinemethanol, an aromatic alcohol compound, is a widely used in the synthesis of some inhibitors like Chk1 and histone deacetylase inhibitors. Uses: 3-pyridinemethanol is a widely used in the synthesis of some inhibitors like chk1 and histone deacetylase inhibitors. Synonyms: pyridin-3-ylmethanol. Grades: 95 %. CAS No. 100-55-0. Molecular formula: C6H7NO. Mole weight: 109.13. |  |
| 4-Hydroxy-4-Methyl-2-Pentanone | Environmental Standards. Alternative Names: Diacetone alcohol. CAS No. 123-42-2. Molecular formula: C6H12O2. Mole weight: 116.16. Catalog: ACM123422. | |
| 4-Isopropylpyrazole | 4-Isopropylpyrazole is a 4-substituted pyrazole that is used as an inhibitor of liver alcohol dehydrogenase. Group: Biochemicals. Grades: Highly Purified. CAS No. 13753-53-2. Pack Sizes: 100mg, 500mg. Molecular Formula: C6H10N2, Molecular Weight: 110.16. US Biological Life Sciences. | Worldwide |
| 5- (Hydroxymethyl) furfuryl alcohol | 5- (Hydroxymethyl) furfuryl alcohol. Group: Biochemicals. Alternative Names: 2, 5-Bis (hydroxymethyl)furan, 2,5-furandimethanol; NSC 40737; NSC 524614. Grades: Highly Purified. CAS No. 1883-75-6. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C6H8O3. US Biological Life Sciences. | Worldwide |
| 6-Amino-1-hexanol | A reagent used in the synthesis of guanidino analogs of roscovitine. Synonyms: H-Acp(6)-ol; NH2-(CH2)6-OH; ζ-Amino-n-hexyl alcohol; 6-Amino-N-caproyl alcohol. Grades: ≥ 99 % (GC). CAS No. 4048-33-3. Molecular formula: C6H15NO. Mole weight: 117.19. | |
| 6-Chloro-1-hexyl-3,3,4,4,5,5-d6 Alcohol | 6-Chloro-1-hexyl-3,3,4,4,5,5-d6 Alcohol. CAS No. 1219794-83-8. Molecular formula: C6H7D6ClO. Mole weight: 142.66. Appearance: Liquid. Purity: 98 atom % D. Density: 1.024 g/cm³. Catalog: ACM1219794838. | |
| 6-Deoxy-L-galactitol | 6-Deoxy-L-galactitol, a sugar alcohol, exhibits promising therapeutic capabilities for the management of diabetic complications. Its ability to manipulate aldose reductase, an enzyme that transfigures glucose to sorbitol impedes the accumulation of sorbitol in cells. Furthermore, studies suggest it could potentially be used as an anti-inflammatory and antioxidant agent. Synonyms: 1-deoxy-d-galactitol; (2R,3S,4R,5S)-hexane-1,2,3,4,5-pentol. CAS No. 13074-06-1. Molecular formula: C6H14O5. Mole weight: 166.17. | |
| 6-Deoxy-L-tallitol | 6-Deoxy-L-tallitol, a remarkable sugar alcohol with immense potential, finds widespread application in the biomedical realm. Championed for its vital role in drug development targeting diabetes, metabolic disorders, and cardiovascular ailments, this compound stands as a cornerstone of scientific progress. Molecular formula: C6H14O5. Mole weight: 166.17. | |
| Acetonylacetone | Acetonylacetone. Synonyms: 2,5-Diketohexane;2,5-Hexadione. CAS No. 110-13-4. Product ID: CDC10-0201. Molecular formula: C6H10O2. Category: Fragrance Agents. Product Keywords: Cosmetic Ingredients; Fragrance Agents; Acetonylacetone; CDC10-0201; 110-13-4; C6H10O2; 2,5-Diketohexane; 2,5-Hexadione; 203-738-3; MFCD00008792; 110-13-4. Purity: ≥98%. Color: Clear yellow to brown. EC Number: 203-738-3. Physical State: Liquid. Solubility: Alcohol: miscible. Storage: Store below 30°C. Boiling Point: 191 °C (lit.). Melting Point: -6--5 °C (lit.). Density: 0.973 g/mL at 25 °C (lit.). Product Description: 2,5-Hexanedione is a major metabolite of the neurotoxic industrial solvent methyl n-butyl ketone. It reacts with amines to yield 2,5-dimethylpyrroles. |  |
| alcohol dehydrogenase [NAD(P)+] | Reduces aliphatic aldehydes of carbon chain length from 2 to 14, with greatest activity on C4, C6 and C8 aldehydes; also reduces retinal to retinol. Group: Enzymes. Synonyms: retinal reductase (ambiguous); aldehyde reductase (NADPH/NADH); alcohol dehydrogenase [NAD(P)]. Enzyme Commission Number: EC 1.1.1.71. CAS No. 37250-10-5. 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-0355; alcohol dehydrogenase [NAD(P)+]; EC 1.1.1.71; 37250-10-5; retinal reductase (ambiguous); aldehyde reductase (NADPH/NADH); alcohol dehydrogenase [NAD(P)]. Cat No: EXWM-0355. |  |
| alcohol dehydrogenase (quinone) | Only described in acetic acid bacteria where it is involved in acetic acid production. Associated with membrane. Electron acceptor is membrane ubiquinone. A model structure suggests that, like all other quinoprotein alcohol dehydrogenases, the catalytic subunit has an 8-bladed propeller structure, a calcium ion bound to the PQQ in the active site and an unusual disulfide ring structure in close proximity to the PQQ; the catalytic subunit also has a heme c in the C-terminal domain. The enzyme has two additional subunits, one of which contains three molecules of heme c. It does not require amines for activation. It has a restricted substrate specificity, oxidizing a few primary alcohols (C2 to C6), but not methanol, secondary alcohols and some aldehydes. It is assayed with phenazine methosulfate or with ferricyanide. Group: Enzymes. Synonyms: type III ADH; membrane associated quinohaemoprotein alcohol dehydrogenase. Enzyme Commission Number: EC 1.1.5.5. 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-0433; alcohol dehydrogenase (quinone); EC 1.1.5.5; type III ADH; membrane associated quinohaemoprotein alcohol dehydrogenase. Cat No: EXWM-0433. | |
| α-cyclodextrin | Cyclodextrins occur as white, practically odorless, fine crystalline powders, having a slightly sweet taste. Some cyclodextrin derivatives occur as amorphous powders. Synonyms: alfadexum; alpha-cycloamylose; alpha-cyclodextrin; alpha-dextrin; Cavamax W6 Pharma; cyclohexaamylose; cyclomaltohexose. CAS No. 10016-20-3. Product ID: PE-0501. Molecular formula: (C6H10O5)6. Mole weight: 972.84. Category: Solubilizing Agents; Stabilizing Agents. Product Keywords: Stabilizers; Solubilizer Excipients; Carrier Excipients; ; PE-0501; α-cyclodextrin; Solubilizing Agents; Stabilizing Agents; (C6H10O5)6; 10016-20-3. UNII: Z1LH97KTRM. Chemical Name: α-cyclodextrin. Grade: Pharmceutical Excipients. Administration route: Injection. Dosage Form: Injection preparations. Source and Preparation: Cyclodextrin is prepared by enzymolysis of amylase using special bacteria. The first step in the preparation of cyclodextrin (food grade), the starch paste is prepared by cyclodextrin glucose-transferase (CGTase, EC 2.4.1.19, CAS 9030-09-5) under controlled pH and temperature conditions. CGTase is derived from recombinant Escherichia coli. CGTase gene of Bacillus occitorella was latent. Alphacyclodextrin is precipitated by the addition of 1-decyl alcohol in an enzymatic reaction. Purification is obtained by solubility in water and reprecipitation. The added 1-decanol was separated from afacyclodextrin by reanalysis and steam dis | |
| Azido-PEG3-alcohol | Azido-PEG3-alcohol is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Group: Azido peg linkers. Alternative Names: 1-Azido-8-hydroxy-3,6-dioxaoctane. CAS No. 86520-52-7. Molecular formula: C6H13N3O3. Mole weight: 175.19. Appearance: Oil. Purity: >90%. IUPACName: 2-[2-(2-Azidoethoxy)ethoxy]ethanol. Canonical SMILES: C(COCCOCCO)N=[N+]=[N-]. Catalog: ACM86520527. | |
| Benzyl Alcohol | Benzyl alcohol, also denoted as BnOH is an aromatic alcohol having formula C6H5CH2OH. It is a colorless liquid with a mild pleasant aromatic odor. Benzyl Alcohol is useful solvent due to its polarity, low toxicity, and low vapor pressure. Benzyl alcohol is used as a solvent in inks, waxes, paints, lacquers, and epoxy coatings. It is also a precursor to many esters and ethers which are used in the soap, perfume, and flavor industries. Uses: General solvent for inks, paints, lacquers, and epoxy resin coatingsA precursor to a variety of esters, used in the soap, perfume, and flavor industries, as well as for pharmaceuticalsA photographic developer. Alternative Names: Phenylmethanol, BnOH, Benzoyl alcohol, Phenyl carbinol, Phenyl methanol. Grades: Industrial Grade, Food Grade, Pharmaceutical Grade. CAS No. 100-51-6. Pack Sizes: 210Kgs Galvanized Steel Drums; 230Kgs HM HDPE Barrels; and ISO Tank. |  |
| Benzyl Alcohol | Benzyl alcohol appears as a clear colorless liquid with a pleasant odor. Slightly denser than water. Flash point 194°F. Boiling point 401°F. Contact may irritate skin, eyes, and mucous membranes. May be slightly toxic by ingestion. Used to make other chemicals.;Liquid;Colourless, clear liquid with a faint, aromatic odour;Liquid;Liquid;COLOURLESS LIQUID WITH CHARACTERISTIC ODOUR.;colourless liquid with a slightly pungent, faint aromatic, fruity odour;A clear colorless liquid with a pleasant odor. Group: Polymers. Product ID: phenylmethanol. Molecular formula: 108.14g/mol. Mole weight: C7H8O; C7H8O; C6H5CH2OH; C6H5CH2OH; C7H8O. C1=CC=C(C=C1)CO. InChI=1S / C7H8O / c8-6-7-4-2-1-3-5-7 / h1-5, 8H, 6H2. WVDDGKGOMKODPV-UHFFFAOYSA-N. | |
| Benzyl Alcohol | Benzyl alcohol is also known as Aromatic Alcohol with the chemical formula C6H5CH2OH. The IUPAC name of this compound is phenyl methanol. At room temperature, benzyl alcohol exists as a Colorless liquid that has a mildly aromatic smell. When this aromatic alcohol is deprotonated, the resulting anion is called a benzylate. CAS No. 100-51-6. Product ID: PE-0052. Molecular formula: C6H5CH2OH. Mole weight: 108.14. Category: Preservatives Excipients. Product Keywords: Pharmaceutical Excipients; Liquid Dosage Form; Injections & Sterile Formulation; Semi-solid Dosage Form; Suppository Bases; Preservatives Excipients; Benzyl Alcohol; PE-0052; C6H5CH2OH; 100-51-6; 100-51-6. Appearance: Colorless transparent liquid. Purity: 99.95%min. EC Number: 202-859-9. Synonym(s): Benzenemethanol; Phenylcarbinol; (hydroxymethyl)benzene. Melting Point: -15°C. Density: 1.042 ~ 1.047 g/cm3. | |
| Benzyl benzoate | Benzyl benzoate is an organic compound with the formula C6H5CH2O2CC6H5. It is the ester of benzyl alcohol and benzoic acid. It forms either a viscous liquid or solid flakes and has a weak, sweet-balsamic odor. It occurs in a number of blossoms (e. g. tuberose, hyacinth) and is a component of Balsam of Peru and Tolu balsam.It is on the World Health Organizations List of Essential Medicines, a list of the most important medication needed in a basic health system. Group: Inhibitors. Alternative Names: Phenylmethyl benzoate. CAS No. 120-51-4. Molecular formula: C14H12O2. Mole weight: 212.24. Appearance: Liquid. Purity: 0.98. IUPACName: Benzyl benzoate. Canonical SMILES: C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2. Density: 1.118 g/ml. ECNumber: 204-402-9. Catalog: ACM120514. | |
| Bis(2-methoxyethyl)amine | Amino Alcohols. Alternative Names: Dimethoxyethylamine, Bis(methoxyethyl)amine, Bis(2-Methoxyethyl)amine, 2,2-Dimethoxydiethylamine, Bis-(2-methoxyethyl)-amine, NCIOpen2_009189, B48207_ALDRICH, Diethylamine, 2,2-dimethoxy-, CID2383, NSC78431, EINECS 203-923-9, Ethanamine, 2-methoxy-N-(2-methoxyethyl)-, NSC 78431, BBR-006860, 2-Methoxy-N-(2-methoxyethyl)ethanamine, Diethylamine, 2,2-dimethoxy- (8CI), 111-95-5. CAS No. 111-95-5. Molecular formula: C6H15NO2. Mole weight: 133.19. Appearance: Colorless to yellow liquid. Purity: 0.96. IUPACName: 2-methoxy-N-(2-methoxyethyl)ethanamine. Density: 0.902 g/mL at 25ºC(lit.). Catalog: ACM111955. | |
| Carbonyl (dihydrido)tris (triphenylphosphine)ruthenium (II) | Catalyst for the arylation (or alkenylation) of anthraquinone and PBI. Catalytic C-C bond formation. Transfer hydrogenative coupling of isoprene to alcohols or aldehydes. Alkanes (and alkenes) from alcohols by tandem hydrogen transfer and condensation. Catalyst for the conversion of primary alcohols and aldehydes into methyl esters. Precatalyst for hydrogen production by means of alcohol dehydrogenation. Group: Ruthenium series catalysts. Alternative Names: 25360-32-1; Carbonyl (dihydrido)tris (triphenylphosphine)ruthenium (II); Carbonyldihydridotris (triphenylphosphine)ruthenium (II); Dihydridocarbonyltris (triphenylphosphine)ruthenium; C55H47OP3Ru; [ (C6H5)3P]3Ru (CO)H2; AKOS024258165; Carbonyl (dihydrido)tris (triphenylphosphine)ruthenium (II). CAS No. 25360-32-1. Molecular formula: C55H49OP3Ru. Mole weight: 919.987g/mol. IUPACName: formaldehyde;ruthenium dihydride;triphenylphosphane. Canonical SMILES: C=O. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [RuH2]. Catalog: ACM25360321. | |
| Catechol-13C6 | Catechol-13C6. Group: Biochemicals. Alternative Names: 1,2-Benzenediol-13C6; Pyrocatechol-13C6; 1,2-Dihydroxybenzene-13C6; 2-Hydroxyphenol-13C6; Oxyphenic Acid-13C6; Phthalhydroquinone-13C6; Phthalic Alcohol-13C6; Pyrocatechin-13C6; o-Benzenediol-13C6; o-Dihydroxybenzene-13C6; o-Dioxybenzene-13C6; o-Hydroquinone-13C6; o-Hydroxyphenol-13C6; o-Phenylenediol-13C6; NSC 1573-13C6. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Chlorodihydrido{(R)-(+)-7-Bis(3, 5-di-t-butylphenyl)phosphino-7'-[(3-methylpyridine-2-ylmethyl)amino]-2, 2', 3, 3'-tetrahydro-1, 1'-spirobiindane}iridium(III), >97% (>99% ee) Ir-(R)-DTB-SpiroPAP-3-Me | Catalyst for the enantioselective synthesis of chiral disubstituted oxa-cyclic ethers Catalyst for the enantioselective hydrogenation for the asymmetric synthesis of Rivastigmine Catalyst for the asymmetric hydrogenation for the synthesis of Crizotinib Catalyst for the asymmetric hydrogenation of α-keto acids Catalyst for the kinetic resolution of racemic aliphatic alcohols via selective asymmetric hydrogenation. Group: Iridium catalysts. Alternative Names: 1396201-63-0;Chlorodihydrido{(R)-(+)-7-Bis(3, 5-di-t-butylphenyl)phosphino-7'-[(3-methylpyridine-2-ylmethyl)amino]-2, 2', 3, 3'-tetrahydro-1, 1'-spirobiindane}iridium(III). CAS No. 1396201-63-0. Molecular formula: C52H67ClIrN2P. Mole weight: 978.763g/mol. IUPACName: (3R)-4'-bis(3,5-ditert-butylphenyl)phosphanyl-N-[(3-methylpyridin-2-yl)methyl]-3,3'-spirobi[1,2-dihydroindene]-4-amine;chloro(dihydrido)iridium. Canonical SMILES: CC1=C (N=CC=C1)CNC2=CC=CC3=C2C4 (CC3)CCC5=C4C (=CC=C5)P (C6=CC (=CC (=C6)C (C) (C)C)C (C) (C)C)C7=CC (=CC (=C7)C (C) (C)C)C (C) (C)C. Cl[IrH2]. Catalog: ACM1396201630. | |
| Chlorodihydrido{(S)-(-)-7-Bis(3, 5-di-t-butylphenyl)phosphino-7'-[(3-methylpyridine-2-ylmethyl)amino]-2, 2', 3, 3'-tetrahydro-1, 1'-spirobiindane}iridium(III), >97% (>99% ee) Ir-(S)-DTB-SpiroPAP-3-Me | Catalyst for the enantioselective synthesis of chiral disubstituted oxa-cyclic ethers Catalyst for the enantioselective hydrogenation for the asymmetric synthesis of Rivastigmine Catalyst for the asymmetric hydrogenation for the synthesis of Crizotinib Catalyst for the asymmetric hydrogenation of α-keto acids Catalyst for the kinetic resolution of racemic aliphatic alcohols via selective asymmetric hydrogenation. Group: Iridium catalysts. Alternative Names: 1418483-59-6;Chlorodihydrido{(S)-(-)-7-Bis(3, 5-di-t-butylphenyl)phosphino-7'-[(3-methylpyridine-2-ylmethyl)amino]-2, 2', 3, 3'-tetrahydro-1, 1'-spirobiindane}iridium(III). CAS No. 1418483-59-6. Molecular formula: C52H67ClIrN2P. Mole weight: 978.763g/mol. IUPACName: [(3S)-4'-bis(3, 5-ditert-butylphenyl)phosphaniumyl-3, 3'-spirobi[1, 2-dihydroindene]-4-yl]-[(3-methylpyridin-2-yl)methyl]azanide; chloro(dihydrido)iridium. Canonical SMILES: CC1=C (N=CC=C1)C[N-]C2=CC=CC3=C2C4 (CC3)CCC5=C4C (=CC=C5)[PH+] (C6=CC (=CC (=C6)C (C) (C)C)C (C) (C)C)C7=CC (=CC (=C7)C (C) (C)C)C (C) (C)C. Cl[IrH2]. Catalog: ACM1418483596. | |
| Cinnamyl alcohol | Cinnamyl alcohol. Synonyms: 3-Phenyl-2-propen-1-ol. CAS No. 104-54-1. Pack Sizes: 5, 100, 500 g in poly bottle. Product ID: CDC10-0195. Molecular formula: C6H5CH=CHCH2OH. Category: Flavoring Chemical Agents. Product Keywords: Cosmetic Ingredients; Flavoring Chemical Agents; Cinnamyl alcohol; CDC10-0195; 104-54-1; C6H5CH=CHCH2OH; 3-Phenyl-2-propen-1-ol; 203-212-3; MFCD00002921; 104-54-1. Purity: 0.98. EC Number: 203-212-3. Physical State: Liquid. Quality Level: 100. Application: Cinnamyl alcohol was used to study the alkylation of 2,4-di-tert-butylphenol by cinnamyl alcohol using aluminum-containing mesoporous ethane-silica catalyst. It was used to study gold nanoparticles supported on titanium dioxide catalysed oxidative coupling of alcohols and amines to form the corresponding imines. Boiling Point: 250 °C (lit.). Melting Point: 30-33 °C (lit.). Density: 1.044 g/mL at 25 °C (lit.). | |
| Cis-3-Hexen-1-Ol | Liquid;Liquid;colourless liquid with a powerful, grassy-green odour. Group: Alkenes. Alternative Names: Leaf alcohol. CAS No. 928-96-1. Molecular formula: C6H12O. Mole weight: 100.16. Appearance: Colorless liquid. Purity: 99%+. IUPACName: (Z)-Hex-3-en-1-ol. Canonical SMILES: CCC=CCCO. Density: 0.848 g/mL at 25 °C(lit.). ECNumber: 213-192-8. Catalog: ACM928961. | |
| Cyclic-Oligo Bis[(1R,2R)-(+)-1,2-cyclohexanediamino-N,N-bis(3,3-di-t-butylsalicylidene) cobalt(III)triflate]-5,5-bis(2-carboxyethyl)ether | Oligomeric catalyst used for the hydrolytic kinetic resolution of terminal epoxides under solvent-free conditions. Oligomeric catalyst used for the synthesis of highly enantioenriched trans-1,2-amino alcohols. Group: Cobalt catalysts. Alternative Names: MFCD28144555;647036-07-5;Cyc.-Oligo Bis[(1R,2R)-1,2-cyclohexanediamino-N,N'-bis(3,3'-di-t-butylsalicylidene) Co(III)OTf]-5,5'-bis(2-carboxyethyl)ether. CAS No. 647036-07-5. Molecular formula: C70H90Co2F6N4O20S2. Mole weight: 1603.475g/mol. IUPACName: cobalt;(4R, 9R, 33R, 38R)-14, 28, 43, 57-tetratert-butyl-13, 29, 42, 58-tetrahydroxy-17, 21, 25, 46, 50, 54-hexaoxa-3, 10, 32, 39-tetrazaheptacyclo[53.3.1.112, 16.126, 30.141, 45.04, 9.033, 38]dohexaconta-1(58), 2, 10, 12, 14, 16(62), 26(61), 27, 29, 31, 39, 41, 43, 45(60), 55(59), 56-hexadecaene-18, 24, 47, 53-tetrone;trifluoromethanesulfonic acid. Canonical SMILES: CC (C) (C)C1=C (C2=CC (=C1)OC (=O)CCOCCC (=O)OC3=CC (=C (C (=C3)C=NC4CCCCC4N=CC5=CC (=CC (=C5O)C (C) (C)C)OC (=O)CCOCCC (=O)OC6=CC (=C (C (=C6)C=NC7CCCCC7N=C2)O)C (C) (C)C)O)C (C) (C)C)O. C (F) (F) (F)S (=O) (=O)O. C (F) (F) (F)S (=O) (=O)O. [Co]. [Co]. Catalog: ACM647036075. | |
| Cyclic-Oligo Bis[(1S,2S)-(-)-1,2-cyclohexanediamino-N,N-bis(3,3-di-t-butylsalicylidene) cobalt(III)triflate]-5,5-bis(2-carboxyethyl)ether | Oligomeric catalyst used for the hydrolytic kinetic resolution of terminal epoxides under solvent-free conditions. Catalyst used for the synthesis of enantioenriched tetrahydrofurans via the intramolecular openings of oxetanes. Catalyst for the enantioselective addition of phenyl carbamate to meso-epoxides for the synthesis of trans-1,2-amino alcohols. Group: Cobalt catalysts. Alternative Names: MFCD28144556;1252661-94-1;Cyc-Oligo Bis[(1S,2S)-(-)-1,2-cyclohexanediamino-N,N'-bis(3,3'-di-t-Busalicylidene) Co(III)OTf]-5,5'-bis(2-carboxyEt)ether;Cyclic-Oligo Bis[(1S,2S)-(-)-1,2-cyclohexanediamino-N,N'-bis(3,3'-di-t-butylsalicylidene) cobalt(III)triflate]-5,5'-bis(2-carboxyethyl)ether. CAS No. 1252661-94-1. Molecular formula: C70H90Co2F6N4O20S2. Mole weight: 1603.475g/mol. IUPACName: cobalt;(4S, 9S, 33S, 38S)-14, 28, 43, 57-tetratert-butyl-13, 29, 42, 58-tetrahydroxy-17, 21, 25, 46, 50, 54-hexaoxa-3, 10, 32, 39-tetrazaheptacyclo[53.3.1.112, 16.126, 30.141, 45.04, 9.033, 38]dohexaconta-1(58), 2, 10, 12, 14, 16(62), 26(61), 27, 29, 31, 39, 41, 43, 45(60), 55(59), 56-hexadecaene-18, 24, 47, 53-tetrone;trifluoromethanesulfonic acid. Canonical SMILES: CC (C) (C)C1=C (C2=CC (=C1)OC (=O)CCOCCC (=O)OC3=CC (=C (C (=C3)C=NC4CCCCC4N=CC5=CC (=CC (=C5O)C (C) (C)C)OC (=O)CCOCCC (=O)OC6=CC (=C (C (=C6)C=NC7CCCCC7N=C2)O)C | |
| Cyclohexanol | Alcohols. Alternative Names: Cyclohexyl Alcohol. CAS No. 108-93-0. Molecular formula: C6H12O. Mole weight: 100.16. Purity: 0.98. Canonical SMILES: C1CCC(CC1)O. Catalog: ACM108930. | |
| Dichloro (N, N, N', N'-tetramethylethylenediamine) palladium (II) | Catalyst for: Cross-coupling reactions. Catalytic reduction reactions. Preparation of silyl ethers via reaction of silicon-hydrogen bond with alcohols. Oxidative carbonylation reactions. Group: Palladium series catalysts. Alternative Names: I14-10025; AC1L4Z7Y; AC1Q1RTB; Palladium, dichloro(N,N,N',N'-tetramethyl-1,2-ethanediamine-N,N')-, (SP-4-2)- (9CI); RL01764; Palladium, dichloro(N, N, N', N'-tetramethylethylenediamine)- (8CI); AKOS015900158; TRA0000186; dichloride. CAS No. 14267-08-4. Molecular formula: C6H16Cl2N2Pd. Mole weight: 293.528g/mol. IUPACName: palladium(2+);N, N, N', N'-tetramethylethane-1, 2-diamine;dichloride. Canonical SMILES: CN(C)CCN(C)C.[Cl-].[Cl-].[Pd+2]. Catalog: ACM14267084. | |
| Dichloro{ (R) -2, 2'-bis [bis (4-methylphenyl) ] -1, 1'-binaphthyl} [ (1R, 2R) -2-amino-1-phenylpropyldiphenylphosphine] ruthenium (II) , min. 97% | Precursor to cationic hydrogenation catalyst for synthesis of chiral alcohols from ketones. Group: Ruthenium catalysts. Alternative Names: MFCD17018805; 1150113-55-5; Dichloro{ (R) -2, 2'-bis [bis (4-methylphenyl) ] -1, 1'-binaphthyl} [ (1R, 2R) -2-amino-1-phenylpropyldiphenylphosphine] ruthenium (II) ; 97%. CAS No. 1150113-55-5. Molecular formula: C69H62Cl2NP3Ru. Mole weight: 1170.153g/mol. IUPACName: [1-[2-bis(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(4-methylphenyl)phosphane;(1R,2R)-1-diphenylphosphanyl-1-phenylpropan-2-amine;ruthenium(2+);dichloride. Canonical SMILES: CC1=CC=C (C=C1)P (C2=CC=C (C=C2)C)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=C (C=C7)C)C8=CC=C (C=C8)C. CC (C (C1=CC=CC=C1)P (C2=CC=CC=C2)C3=CC=CC=C3)N. [Cl-]. [Cl-]. [Ru+2]. Catalog: ACM1150113555. | |
| Dichloro[ (R)- (+)-2, 2'-bis (diphenylphosphino)-1, 1'-binaphthyl][ (1R, 2R)- (+)-1, 2-diphenylethylenediamine]ruthenium (II), min. 90% | Sequential asymmetric hydrogenation reactions with solution or polymer-bound BINAP/Diamine complexes. Asymmetic hydrogenation of imines. Catalysts for deracemization of benzylic alcohols. Group: Ruthenium series catalysts. Alternative Names: 735D877; Dichloro[(S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl][(1R,2R)-(+)-1,2-diphenylethylenediamine] ruthenium(II), 95%; SC10163; C58H48Cl2N2P2Ru; Dichloro[ (R)- (+)-2, 2'-bis (diphenylphosphino)-1, 1'-binaphthyl][ (1R, 2R)- (+)-1, 2-diphenylethylenediamine)ruthenium (II); J-013922; RUCL2((S)-BINAP)(R,R-DPEN); DICHLORO[ (R)- (+)-2, 2-BIS (DIPHENYLPHOSPHINO)-1, 1'-BINAPHTHYL][ (1R, 2R)- (+)-1, 2-DIPHENYLETHYLENEDIAMINE]RUTHENIUM (II). CAS No. 212143-23-2. Molecular formula: C58H48Cl2N2P2Ru. Mole weight: 1006.954g/mol. IUPACName: dichlororuthenium;(1R,2R)-1,2-diphenylethane-1,2-diamine;[1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)C (C (C2=CC=CC=C2)N)N. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=CC=C7)C8=CC=CC=C8. Cl[Ru]Cl. Catalog: ACM212143232. | |
| D-Iditol | D-Iditol is a sugar alcohol mainly utilized in pharmaceutical preparations as an excipient due to its stabilizing and moisturizing properties. Additionally, D-Iditol has been studied for its potential use in the research of various diseases, including diabetes and metabolic disorders. CAS No. 25878-23-3. Molecular formula: C6H14O6. Mole weight: 182.17. | |
| Dihydroxybis(hydrogen Lactato)titanium(IV) (ca. 44% in Isopropyl Alcohol, Water) | Dihydroxybis(hydrogen Lactato)titanium(IV) (ca. 44% in Isopropyl Alcohol, Water). Group: Salt. CAS No. 79110-90-0. Product ID: 2-hydroxypropanoate; titanium(4+); dihydroxide. Molecular formula: 260.02g/mol. Mole weight: C6H12O8Ti. CC(C(=O)[O-])O. CC(C(=O)[O-])O. [OH-]. [OH-]. [Ti+4]. InChI=1S/2C3H6O3. 2H2O. Ti/c2*1-2(4)3(5)6; ; ; /h2*2, 4H, 1H3, (H, 5, 6); 2*1H2; /q; ; ; ; +4/p-4. DTQHSUHILQWIOM-UHFFFAOYSA-J. | |
| D-Leucinol | The alcohol form of D-Leucine, a dietary amino acid involved in human protein synthesis. Synonyms: 1-Pentanol, 2-amino-4-methyl-, (2R)-. Grades: ≥ 99 % (Assay). CAS No. 53448-09-2. Molecular formula: C6H15NO. Mole weight: 117.2. | |
| D-Talitol | D-Talitol, a remarkably versatile sugar alcohol, finds extensive application as an excipient in diverse pharmaceutical formulations. Renowned for its profound efficacy in augmenting the flavor of oral drugs, it frequently serves as an agent to enhance the taste of chewable tablets and syrups to facilitate greater palatability. Moreover, D-Talitol assumes a pivotal role in the synthetic fabrication of numerous bioactive compounds, thereby showcasing its indispensable role in combating an assortment of diseases. Synonyms: D-Altritol. CAS No. 643-03-8. Molecular formula: C6H14O6. Mole weight: 182.17. | |
| furan resin | Furfuryl alcohol appears as a clear colorless liquid. Flash point 167°F. Boiling point 171°F. Denser than water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion and skin contact and moderately toxic by inhalation.; Liquid; Liquid; Liquid; Liquid; COLOURLESS LIQUID WITH CHARACTERISTIC ODOUR. TURNS RED OR BROWN ON EXPOSURE TO LIGHT AND AIR.;Colourless or pale yellowish liquid, mild, warm oily, "burnt" odour;Colorless to amber liquid with a faint, burning odor.;Colorless to amber liquid with a faint, burning odor. [Note: Darkens on exposure to light.]. Group: Polymers. CAS No. 25212-86-6. Product ID: furan-2-ylmethanol. Molecular formula: 98.1g/mol. Mole weight: C5H6O2;C5H6O2. C1=COC(=C1)CO. InChI=1S / C5H6O2 / c6-4-5-2-1-3-7-5 / h1-3, 6H, 4H2. XPFVYQJUAUNWIW-UHFFFAOYSA-N. | |
| furfuryl alcohol resin | Furfuryl alcohol appears as a clear colorless liquid. Flash point 167°F. Boiling point 171°F. Denser than water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion and skin contact and moderately toxic by inhalation.; Liquid; Liquid; Liquid; Liquid; COLOURLESS LIQUID WITH CHARACTERISTIC ODOUR. TURNS RED OR BROWN ON EXPOSURE TO LIGHT AND AIR.;Colourless or pale yellowish liquid, mild, warm oily, "burnt" odour;Colorless to amber liquid with a faint, burning odor.;Colorless to amber liquid with a faint, burning odor. [Note: Darkens on exposure to light.]. Group: Polymers. CAS No. 25212-86-6. Product ID: furan-2-ylmethanol. Molecular formula: 98.1g/mol. Mole weight: C5H6O2;C5H6O2. C1=COC(=C1)CO. InChI=1S / C5H6O2 / c6-4-5-2-1-3-7-5 / h1-3, 6H, 4H2. XPFVYQJUAUNWIW-UHFFFAOYSA-N. | |
| Hexabromobenzene | Monoclinic needles or white powder. Insoluble in water. (NTP, 1992). Group: Amino alcohols. Alternative Names: Benzene, hexabromo-. CAS No. 87-82-1. Molecular formula: C6Br6. Mole weight: 551.5. Purity: 0.98. IUPACName: 1,2,3,4,5,6-Hexabromobenzene. Canonical SMILES: C1(=C(C(=C(C(=C1Br)Br)Br)Br)Br)Br. Density: 2.956 g/cm3. ECNumber: 201-773-9. Catalog: ACM87821-1. | |
| Hexyl alcohol | Hexyl alcohol. Group: Biochemicals. Alternative Names: 1-Hexanol. Grades: Highly Purified. CAS No. 111-27-3. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C6H14O. US Biological Life Sciences. | Worldwide |
| Indulin | Heterocyclic Organic Compound. Alternative Names: ANILINE BLUE 2B;ACID BLUE 20;CI 50405;CI NO 50405;INDULINE;INDULINE (WATER SOLUBLE);INDULIN, WATER SOLUBLE;INDULIN. CAS No. 12771-92-5. Molecular formula: C30H25N6.Cl. Mole weight: 505.022. Purity: alcohol soluble. IUPACName: 7-N,8-N,5-triphenylphenazin-5-ium-2,3,7,8-tetramine;chloride. Canonical SMILES: C1=CC=C (C=C1) NC2=CC3=NC4=CC (=C (C=C4[N+] (=C3C=C2NC5=CC=CC=C5) C6=CC=CC=C6) N) N. [Cl-]. ECNumber: 232-333-4. Catalog: ACM12771925. | |
| Lactitol-13C6 | Lactitol-13C6 is labelled Lactitol which is listed as an excipient in some prescription drugs, such as Adderall. Lactitol is a sugar alcohol used as a replacement bulk sweetener for low calorie foods. It is also used medically as a laxative. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C613C6H24O11, Molecular Weight: 350.27. US Biological Life Sciences. | Worldwide |
| L-Glucitol | L-Glucitol is L-Isomer of D-Glucitol (S677100), a sugar alcohol obtained from the reduction of glucose and is naturally found in various fruits such as apples, pears and peaches. Group: Biochemicals. Grades: Highly Purified. CAS No. 6706-59-8. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C6H14O6, Molecular Weight: 182.17. US Biological Life Sciences. | Worldwide |
| L-Histidinol | L-histidinol has a role as a glycylpeptide N-tetradecanoyltransferase inhibitor, a human metabolite, an Escherichia coli metabolite and a Saccharomyces cerevisiae metabolite. It is also a member of imidazoles and an amino alcohol. It is a conjugate base of a L-histidinol(1+). Synonyms: (S)-histidinol; (S)-beta-Amino-1H-imidazole-4-propanol; 1H-Imidazole-4-propanol, beta-amino-, (S)-. CAS No. 4836-52-6. Molecular formula: C6H11N3O. Mole weight: 141.17. | |
| L-Iditol | L-Iditol, known as a pharmaceutical excipient and nutrient additive, showcases its versatility in the sphere of medical applications. Its intrinsic stabilizing properties render it a trusted component in tablet and capsule fabrication. Synonyms: L-Iditol; 488-45-9; Iditol; (2S,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol; Hexahydroxyhexane; 1Q2H9GC12E; (2S,3R,4R,5S)-hexane-1,2,3,4,5,6-hexaol; MFCD00064289; Karion; Hexahydric alcohol; L-Idit; IDITOL, L-; L-Iditol, >=98%; UNII-1Q2H9GC12E; SCHEMBL435775; CHEBI:18202; FBPFZTCFMRRESA-UNTFVMJOSA-N; DTXSID901337629; AKOS024258141; AS-56025; HY-121654; CS-0082969; I0725; C01507; D91196; W-202860; Q27102896. CAS No. 488-45-9. Molecular formula: C6H14O6. Mole weight: 182.17. | |
| L-Mannitol | L-Mannitol, a versatile sugar alcohol, has found its way into a plethora of biomedical applications. Exhibiting its potency as an osmotic diuretic, this compound is efficacious against cerebral edema and glaucoma. However, L-Mannitol isn't just a one-trick pony; it has been extensively used as an excipient in various pharmaceutical formulations for optimizing the solubility and stability of drugs. Furthermore, the substance has drawn considerable attention as a promising therapeutic agent unparalleled for addressing cystic fibrosis and diabetes. Synonyms: Mannitol, L-; L-manno-Hexitol. Grades: ≥96%. CAS No. 643-01-6. Molecular formula: C6H14O6. Mole weight: 182.17. | |
| L-Rhodinose | L-Rhodinose is an innate sugar alcohol emanating enticing prospects for studying metabolic ailments and diabetes. Synonyms: 2,3,6-Trideoxy-L-threo-hexose. Molecular formula: C6H12O3. Mole weight: 132.16. | |
| Lysine hydrochloride | Lysine hydrochloride. Uses: For analytical and research use. Group: European pharmacopoeia (ph. eur.); pharmacopoeial standards. Alternative Names: Saturated Aminoalcohol Hydrochloride, Lysion, Bovi-Lysine, L-Lysine hydrochloride, Lyamine, Acetamido Alcohol, NSC 9253, (S)-2,6-diaminohexanoic acid hydrochloride, L-(+)-Lysine monohydrochloride, Aminoalcohol Hydrochloride, Darvyl, Lysine hydrochloride, L-Lysine, monohydrochloride (9CI), Lysine, monohydrochloride, L- (8CI), Lysine Dihydrochloride, L-Gen,L-Lysine, hydrochloride (1:1), Lysine monohydrochloride, Relys, Trans-Amininoalcohol Hydrochloride, Lysine hydrochloride, Conjugated Amino Acid, Amino Acid, L-Lysine monohydrochloride. CAS No. 657-27-2. IUPAC Name: (2S)-2,6-diaminohexanoic acid;hydrochloride. Molecular Formula: C6H14N2O2.ClH. Mole Weight: 182.65. Catalog: APS657272. SMILES: Cl.NCCCC[C@H](N)C(=O)O. Format: Neat. Shipping: Room Temperature. |  |
| Mannitol | Mannitol is D-mannitol. It is a hexahydric alcohol related to mannose and is isomeric with sorbitol. Mannitol occurs as a white, odorless, crystalline powder, or freeflowing granules. It has a sweet taste, approximately as sweet as glucose and half as sweet as sucrose, and imparts a cooling sensation in the mouth. Synonyms: Cordycepic acid; E421; Emprove; manna sugar; D-mannite; mannite; mannitolum; Mannogem; Pearlitol. CAS No. 69-65-8. Product ID: PE-0479. Molecular formula: C6H14O6. Mole weight: 182.17. Category: Diluent; Plasticizer; Sweetening Agents; Tablet and Capsule Diluent. Product Keywords: Sweeteners Excipients; Stabilizers; PE-0479; Mannitol; Diluent; Plasticizer; Sweetening Agents; Tablet and Capsule Diluent; C6H14O6; 69-65-8. UNII: 3OWL53L36A. Chemical Name: D-Mannitol. Grade: Pharmceutical Excipients. Administration route: IP, IM, IV, and SC; infusions; buccal, oral and sublingual; ophthalmic; topical. Dosage Form: IP, IM, IV, and SC injections; infusions; buccal, oral and sublingual tablets, powders and capsules; ophthalmic preparations; topical solutions. Stability and Storage Conditions: Mannitol is stable in the dry state and in aqueous solutions. Solutions may be sterilized by filtration or by autoclaving and if necessary may be autoclaved repeatedly with no adverse physical or chemical effects. In solution, mannitol is not attacked by cold, dilute acids or alkalis, nor by atmospheric oxygen in the abs | |
| N-(4-Hydroxybutyl)trifluoroacetamide | N-(4-Hydroxybutyl)trifluoroacetamide (CAS# 128238-43-7 ) is a useful research chemical. Synonyms: Tfa-Abu(4)-ol; Tfa-NH-(CH2)4-OH; 4-(Trifluoroacetylamino)-1-butanol; δ-(Trifluoroacetylamino)-n-butyl alcohol; 2,2,2-trifluoro-N-(4-hydroxybutyl)acetamide. Grades: 95 %. CAS No. 128238-43-7. Molecular formula: C6H10F3NO2. Mole weight: 185.15. | |
| Pyridine-2-methanol 1-oxide | Heterocyclic Organic Compound. Alternative Names: 2-(Hydroxymethyl)pyridine 1-Oxide; 2-Pyridinemethanol 1-Oxide; 2-Pyridylcarbinol N-Oxide; 2-Pyridylmethanol N-Oxide; 2-Picolyl Alcohol 1-Oxide. CAS No. 10242-36-1. Molecular formula: C6H7NO2. Mole weight: 125.13. Appearance: White Solid. Purity: 0.96. IUPACName: (1-oxidopyridin-1-ium-2-yl)methanol. Canonical SMILES: C1=CC=[N+](C(=C1)CO)[O-]. Density: 1.18g/cm³. ECNumber: 233-580-0. Catalog: ACM10242361. | |
| Pyridinium trifluoromethanesulfonate, min. 97% | Catalytic amounts of pyridinium triflate in conjunction with silylbenzamide is a versatile reagent for the silylation of alcohols. Group: Heterocyclic organic compound. Alternative Names: CTK1G8962; AKOS015852954; AC1MC242; FT-0700859; SCHEMBL318231; TR-018537; YWVYZMVYXAVAKS-UHFFFAOYSA-N; Pyridinium triflate; ACMC-209ky5. CAS No. 52193-54-1. Molecular formula: C6H6F3NO3S. Mole weight: 229.173g/mol. IUPACName: pyridin-1-ium;trifluoromethanesulfonate. Canonical SMILES: C1=CC=[NH+]C=C1. C(F)(F)(F)S(=O)(=O)[O-]. Catalog: ACM52193541. | |
| Quinoline-13C3,15N | Isotope labelled Quinoline (Q700380), which is a starting material that may be transformed by bacteria and fungi to produce intermediates useful for the synthesis of drugs. Used in the synthesis of tertiary alcohol modulators of RORγ (1) which appears to have various biological functions. Also derivatives of quinoline have been seen to promote anticancer, antibacterial and antiviral activity, however quinoline itself is often seen as an environmental contaminant (2,3). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C613C3H715N. US Biological Life Sciences. | Worldwide |
| (R)-(+)-2-Diphenylphosphino-2'-methoxy-1,1'-binaphthyl | 1. Efficient catalyst for the enantoselective hydrosilyation of 1-alkenes to optically active 2-alcohols. 2. Ligand for palladium-catalyzed asymmetric reduction of allyltc esters. 3. Ligand for the rhodium-catalyzed asymmetric aryiation of imines with organostannanes. 4. Ligand for the rhodiunvcatalyzed asymmetrk: addition of aryl- and alkenyiborontc acids to Isatins. 5. Ligand for desymmetrizatlon of malonamides via an enantiosetective intramolecular Buchwatd-Hartwig reaction. Group: Heterocyclic organic compound. CAS No. 145964-33-6. Molecular formula: C33H25OP. Mole weight: 468.536g/mol. IUPACName: [1-(2-methoxynaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Canonical SMILES: COC1=C (C2=CC=CC=C2C=C1)C3=C (C=CC4=CC=CC=C43)P (C5=CC=CC=C5)C6=CC=CC=C6. Catalog: ACM145964336. | |
| (R)-3, 3'-Bis(3, 5-diisopropylphenyl)-[1, 1'-binapthalene]-2, 2'-diol | (R)-3, 3'-Bis(3, 5-diisopropylphenyl)-[1, 1'-binapthalene]-2, 2'-diol, also known as (R)-BINAP, is an important chiral ligand used in asymmetric synthesis of organic compounds. It is a widely used compound in chemical and pharmaceutical industries due to its ability to catalyze a variety of reactions with high enantioselectivity. This review will discuss the synthesis of (R)-BINAP, its scientific research applications, its mechanism of action, its biochemical and physiological effects, the advantages and limitations for lab experiments, and the potential future directions of research. Uses: (r)-binap is widely used in asymmetric synthesis of various organic compounds, including chiral drugs, natural products, and polymers. it is particularly useful in the synthesis of polycyclic compounds and chiral alcohols, and has been used in the synthesis of a variety of drugs, including the antimalarial drug artemisinin, the anti-cancer drug paclitaxel, and the anti-hiv drug tenofovir. in addit. Group: Chiral binol ligands. CAS No. 1435948-31-4. Molecular formula: C44H46O2. Mole weight: 606.8 g/mol. IUPACName: 3-[3,5-di(propan-2-yl)phenyl]-1-[3-[3,5-di(propan-2-yl)phenyl]-2-hydroxynaphthalen-1-yl]naphthalen-2-ol. Canonical SMILES: CC (C)C1=CC (=CC (=C1)C2=CC3=CC=CC=C3C (=C2O)C4=C (C (=CC5=CC=CC=C54)C6=CC (=CC (=C6)C (C)C)C (C)C)O)C (C)C. Catalog: ACM1435948314-1. | |
| RuCl2[(S)-xylbinap][(S,S)-dpen] | Sequential asymmetric hydrogenation reactions with solution or polymer-bound BINAP/Diamine complexes. Asymmetic hydrogenation of imines. Catalysts for deracemization of benzylic alcohols. Group: Ruthenium series catalysts. Alternative Names: MFCD09753028; RUCL2[(S)-XYLBINAP][(S,S)-DPEN]; RuCl2[(S)-(DM-BINAP)][(S,S)-DPEN]; Dichloro[(S)-(-)-2,2 inverted exclamation marka-bis[di(3,5-xylyl)phosphino]-1,1 inverted exclamation marka-binaphthyl][ (1S, 2S)- (-)-1, 2-diphenylethylenediamine]ruthenium (II); Dichloro{ (S)- (-)-2, 2'-bis[di (3, 5-xylyl)phosphino]-1, 1'-binaphthyl}[ (1S, 2S)- (-)-1, 2-diphenylethylenediamine]ruthenium (II); (S)-DM-BINAP RuCl2 (S,S)-DPEN; C66H64N2P2Ru Cl2. CAS No. 220114-03-4. Molecular formula: C66H64Cl2N2P2Ru. Mole weight: 1119.17g/mol. IUPACName: [1-[2-bis(3, 5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3, 5-dimethylphenyl)phosphane; dichlororuthenium; (1S, 2S)-1, 2-diphenylethane-1, 2-diamine. Canonical SMILES: CC1=CC (=CC (=C1)P (C2=C (C3=CC=CC=C3C=C2)C4=C (C=CC5=CC=CC=C54)P (C6=CC (=CC (=C6)C)C)C7=CC (=CC (=C7)C)C)C8=CC (=CC (=C8)C)C)C. C1=CC=C (C=C1)C (C (C2=CC=CC=C2)N)N. Cl[Ru]Cl. Catalog: ACM220114034. | |
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