British Abstracts: Pure chemistry and physiology. ser. A1932 |
Từ bên trong sách
Kết quả 1-3 trong 99
Trang 845
... diazotised + a - naphthol . Orange II . Sulphanilic acid diazotised + B - naphthol . Orange III . See Methyl orange . Orange No. 3. m - Nitraniline diazotised + R acid . Orange IV . See Diphenylamine orange . Orange G. Aniline ...
... diazotised + a - naphthol . Orange II . Sulphanilic acid diazotised + B - naphthol . Orange III . See Methyl orange . Orange No. 3. m - Nitraniline diazotised + R acid . Orange IV . See Diphenylamine orange . Orange G. Aniline ...
Trang 1627
... diazo derivatives of amidoanthra- quinone sulphonic acids on naphthol sulphonic acids . 1,389 , Jan. 19 , 1904 , Farbenfabriken . - Fast red dyestuffs for lakes . Produced by coupling diazotised o - amidobenzoic acid with a - naphthol ...
... diazo derivatives of amidoanthra- quinone sulphonic acids on naphthol sulphonic acids . 1,389 , Jan. 19 , 1904 , Farbenfabriken . - Fast red dyestuffs for lakes . Produced by coupling diazotised o - amidobenzoic acid with a - naphthol ...
Trang 989
... diazotised + a - naphthol . Orange II . Sulphanilic acid diazotised + B - naphthol . Orange III . See Methyl orange . Orange No. 3. m - Nitraniline diazotised + R acid . Orange IV . See Diphenylamine orange . Orange G. Aniline ...
... diazotised + a - naphthol . Orange II . Sulphanilic acid diazotised + B - naphthol . Orange III . See Methyl orange . Orange No. 3. m - Nitraniline diazotised + R acid . Orange IV . See Diphenylamine orange . Orange G. Aniline ...
Nội dung
Kinetic Theory Thermodynamics | 9 |
Electrochemistry | 23 |
Reactions | 336 |
20 phần khác không được hiển thị
Ấn bản in khác - Xem tất cả
Thuật ngữ và cụm từ thông dụng
A. A. ELDRIDGE A. B. D. CASSIE absorption Ac derivative Ac₂O acetate acid AcOH action activity adsorption affords alcohol aldehyde alkali Amer approx atoms Biochem Biol C. A. SILBERRAD C. J. WEST calc catalytic CHCl3 Chem CHEMICAL ABSTRACTS Chim chloride CO₂ coeff colloidal compounds Compt conc concn const containing converted cryst crystals CUTHILL decomp decreases determined diazotised E. S. HEDGES effect electrolytes electrons enzyme ergosterol ester ether EtOH F. O. HowITT formation formed gives glucose glycerol H. F. GILLBE H₂ H₂O H₂SO heated hydrochloride hydrogen hydrolysis increase ions isomerisation ketone L. S. THEOBALD liquid MeOH method mixture N. M. BLIGH NaOH nitrate obtained oxidation oxidised oxime phenols Physical Rev Physik picrate piperidine prep prepared presence protein pyridine reaction reduced rend salts semicarbazone solution substance velocity viscosity whilst yield Zentr