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NAKAMURA SCIENTIFIC INSTRUMENT CO., LTD.

Directory

Oxidation, Heavy metal compound / No-pressure distillation / High temperature reaction (over 200 C degree) / Radical polymerization / Drying, (No-pressure/Vacuum) / Hydrogenation / Bromination / Ullman reaction / Enzymatic reaction / Inorganic compound / Waste treatment / Synthesis of chemical reagent and pharmaceutical intermediate / Preparative crude refining / Optical microscope / Differential scanning calorimetry(DSC) / Liquid chromatography analysis(LC) / Color difference / Hydrogen cyanide, Sodium cyanide, Potassium cyanide / Reduction, Nitro compound / Azidation / Mizoroki-Heck reaction / Kumada-Tamao-Corriu cross coupling / Flow synthesis / Oxidation, Peroxide / Vacuum distillation / Reduction, Metalic hydride / Low temperature reaction (over -20 C degree) / Anionic polymerization / Nitration / Acylation / Organic lithium / Oganic sulfur compound / Chiral synthesis / Chromatography / Purification, Preparative Isolation / Inductively coupled plasma-atomic emission spectrometry / Gas chromatography analysis / Karl Fischer moisture analysis / freeze-drying / Negishi cross coupling / Glaser reaction / Rectification / Ammoxidation / Reduction, Catalytic / High-pressure reaction / Cationic polymerization / Column purification / Diazotization / Grignard reaction / Optical resolution / Solvent recovery / Hydrogen sulfate / Inductively coupled plasma-plasma mass spectrometrv(ICP-MS) / Gravimetric analysis(GA) / Head Space Gas Chromatography(HS/GC) / Organosilicon compound / Acetalization / Migita-Kosugi-Stille cross coupling / Hydrogeneration / Oxidization, Air / Living polymerization / Film distillation / Iodination / Acid chlorides / Reaction, NaNH2 / Acetylenic chemistry / Carbon disulfide / Alcohol recycling / Ultraviolet-Visible spectrophotometer(UV-VIS) / Liquid chromatography analysis-mass spectrometry(LC-MS) / Drying capacity / Thermogravimetric analysis(TG) / Diazo-coupling reaction / Diazocoupling / Sonogashira-Hagihara Cross Coupling / Polycondensation / Oxidization, Halogenide / Reduction, High-pressure / Fluorine compound / Reaction, NaH / Active sludge process / Suzuki-Miyaura cross coupling / Sandmeyer reaction / Infrared spectroscopy(IR) / Gas chromatography analysis-mass spectrometry(GC-MS) / Halogenate, Diverse halogenating agents / Mercaptan / Amidination / Dehydrogenation / Reduction, High/Middle-pressure / Emulsion polymerization / Molecular distillation / Amination / Sulfonation / Organic sodium / Phosphoric compound / Pollution prevention / Sublimation / Halogenate, Thionyl chloride, Sulfuryl chloride etc / Buchwald-Hartwig cross coupling / Oxidation, Swern / Suspension polymerization / Extraction / Consultation, Waste / Gas absorption / Thiophosgene / Combustion heat / Halogenate, NCS, NBS, NCI etc / Chlorosulfonation / Allylation / Oxidation, Ozone / Solution polymerization / Crystallization / Alkylation / Ethylene oxide / Sulfonamidation / Chiral compound / Oxidation, Nitric acid / Reduction, Birch / Aldol reaction / Flexibility / Gel permation chromatography(GPC) / Nitrosation / Depolymerization / Wittig reaction / Wolff-Kishner-reduction / Thin layer chromatograph(TLC) / Fusing point / Oxidation, Jones / Etherfication / Gel filtration chromatography(GFC) / Coagyulation point / Recrystallization / Esterification / Oppenauer oxidation / Epoxidation / Filtration / Baeyer-Villiger oxidation / Hyroxylation, Microorganism enzyme / Metal contents reduction / Carbonylation / Cannizarro reaction / Guanidination / Knoevenagel condensation / Kolbe-Schmitt reaction / Silylation / Schiemann reaction / Strecker reaction / Diels-Alder / Tishchenko reaction / Cyanation / Perkin reaction / Hydroxyethylation / Hydroxymethylation / Hydroxylation / Vilsmeier reaction / Fries rearrangement / Friedel-Crafts reaction / Hoesch reaction / Hofmann's Reaction / Formylation / Michael addition / Mannich reaction / Methylolation / Racemization / Leuckart reaction / Cyclization / Ring-Opening reaction / Dealkylation / Dehalogenation / Dehydration / Rearrangement / Acid amide / Dehydrogenation / Decarbonation / Quaternarization of Amine, Benzyl oxide /

Company Information

  • 103-0001 Nakamura Building, 18-10 Nihonbashi-kodenma-cho, Chuo-ku, Tokyo 103-0001
  • Tel.81-3-3661-4662 Fax.81-3-3661-0369
  • website