
CAS Name: N-Ethyl-N-nitrosoethanamine
Additional Names: diethylnitrosamine
Trademarks: DEN; DENA; NDEA
Percent Composition: C 47.04%, H 9.87%, N 27.43%, O 15.66%
Literature References: Detected in trace amounts in tobacco smoke: Druckney, Preussman, Naturwissenschaften 49, 498 (1962) and in various processed foods: Hedler, Marquardt, Food Cosmet. Toxicol. 6, 341 (1968); Friemuth, Glaeser, Nahrung 14, 357 (1970). Formed by the interaction of nitrite with diethylamine and by the action of nitrate-reducing bacteria. Industrial prepn: Reilly, DE 1085166 (1960 to du Pont), C.A. 56, 4594h (1962); Levering, Maury, US 3090786 (1963 to Hercules Powder); Minisci, Galli, Chim. Ind. (Milan) 46, 173 (1964). Hepatotoxicity and carcinogenicity studies: Schmaehl et al., Naturwissenschaften 54, 341 (1967); Grover, Fischer, Eur. J. Cancer 7, 77 (1971); Bader et al., Arch. Geschwulstforsch. 37, 327 (1971). General review: Magee, Barnes, Adv. Cancer Res. 10, 163-246 (1967).
CAS Name: 2,3-Dimercapto-1-propanol
Additional Names: 1,2-dithioglycerol; British anti-lewisite; BAL
Trademarks: Dicaptol (Chinoin); Sulfactin (Viatris)
Percent Composition: C 29.00%, H 6...
Literature References: Developed as an antidote to the vesicant warfare agent, dichloro(2-chlorovinyl)arsine, q.v., also known as Lewisite. Inhibits the toxic action of arsenic on pyruvate dehydrogenase. Discovery and development: R. A. Peters et al., Nature 156, 616 (1945); L. L. Waters, C. Stock, Science 102, 601 (1945). Prepn by hydrogenation of hydroxypropylene trisulfide: W. J. Peppel, F. K. Signaigo, US 2402665 (1946 to DuPont). Stereospecific synthesis: A. K. M. Anisuzzaman, L. N. Owen, J. Chem. Soc. C 1967, 1021. GC/MS determn in plasma: C. E. Byers et al., J. Anal. Toxicol. 28, 384 (2004). Toxicity study: P. Zvirblis, R. I. Ellin, Toxicol. Appl. Pharmacol. 36, 297 (1976). Review of discovery, biochemistry and clinical applications: J. A. Vilensky, K. Redman, Ann. Emerg. Med. 41, 378-383 (2003).
CAS Name: Arabinitol
Additional Names: 1,2,3,4,5-pentanepentol; arabite
Percent Composition: C 39.47%, H 7.95%, O 52.58%
Literature References: D-Form obtained by reduction of D-arabinose or D-lyxose with sodium amalgam: Ruff, Ber. 32, 555 (1899); Ruff, Ollendorff, Ber. 33, 1802 (1900); Bertrand, Bull. Soc. Chim. [3] 15, 593 (1896). Production by fermentation from molasses using Saccharomyces rouxii and Saccharomyces mellis: Lavin, Holloway, US 2934474 (1960 to Comm. Solvents). L-Form obtained by reduction of L-arabinose with sodium amalgam: Kiliani, Ber. 20, 1234, 1571 (1887). DL-Form obtained from equal parts of D- and L-arabitol: Ruff, loc. cit. Synthesis: Lespian, Compt. Rend. 206, 1773 (1938).
CAS Name: 6,7,7a,8-Tetrahydro-10,11-dimethoxy-7-methyl-5H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline
Additional Names: 9,10-dimethoxy-1,2-(methylenedioxy)aporphine; 1,2-methylenedioxy-9,10-di...
Literature References: d-Form prevalent in nature. Found in Dicentra pusilla Sieb. Zucc., Fumariaceae and several other Dicentra species. Related to actinodaphnine, and laurotetanine, q.q.v. Isoln: Y. Asahina, Arch. Pharm. 247, 201 (1909). Isoln of l-form from Duguetia A. St. Hil., Annonaceae: Casagrande, Ferrari, Farmaco Ed. Sci. 25, 442 (1970). Synthesis of dl-form: Haworth et al., J. Chem. Soc. 127, 2018 (1925); Cava et al., Tetrahedron 29, 2245 (1973). Resolution of isomers: Haworth et al., J. Chem. Soc. 129, 29 (1926).
CAS Name: (6aS)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo[de,g]quinoline
Additional Names: 1,2,9,10-tetramethoxyaporphine; boldine dimethyl ether
Trademarks: Bromcholitin...
Literature References: d-Form prevalent in nature. Found in Glaucium flavum Crantz (G. luteum Scop.), Papaveraceae and in Dicentra and Corydalis species, Fumariaceae. Isoln: Fischer, Arch. Pharm. 239, 426 (1901). Structure and prepn: Gadamer, ibid. 249, 680 (1911); Späth, Tharrer, Ber. 66, 904 (1933). Configuration: Faltis, Adler, Arch. Pharm. 284, 281 (1951). Synthesis of dl-form: Chan, Maitland, J. Chem. Soc. C 1966, 753; Jackson, Martin, ibid. 2061; Cava et al., J. Org. Chem. 35, 175 (1970). Pharmacology and toxicity of dl-glaucine phosphate: Y. Kasé et al., Arzneim.-Forsch. 33, 936 (1983). Sites of antitussive action: eidem, ibid. 947.
CAS Name: 4,5-Bis(acetyloxy)-9,10-dihydro-9,10-dioxo-2-anthracenecarboxylic acid
Additional Names: 9,10-dihydro-4,5-dihydroxy-9,10-dioxo-2-anthroic acid diacetate; 1,8-diacetoxy-3-carboxyanthra...
Literature References: Diacetyl derivative of rhein, q.v. Demonstrates anti-arthritic activity without inhibiting prostaglandin synthesis. Prepn: A. Tschirch, K. Heuberger, Arch. Pharm. 240, 596 (1902); V. K. Murty et al., Tetrahedron 23, 515 (1967). Effect on prostaglandin release: P. Pomarelli et al., Farmaco Ed. Sci. 35, 836 (1980). Inhibition of proteases: L. Raimondi et al., Pharmacol. Res. Commun. 14, 103 (1982). Use in arthritis: C. A. Friedmann, DE 2711493; idem, US 4244968 (1977, 1981 both to Proter). Preliminary clinical study in osteoarthritis: A. G. Kay et al., Curr. Med. Res. Opin. 6, 548 (1980). Use in multiple sclerosis, amyotrophic lateral sclerosis: C. A. Friedmann, US 4346103 (1982); idem, JP Kokai 83 225015 (1983 to Proter), C.A. 100, 144991e (1984). Clinical trial in osteoarthritis: S. Adami et al., Clin. Ter. 112, 439 (1985).
CAS Name: 3,4-Dihydro-5-methyl-2H-1-benzopyran-6-carboxylic acid 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide
Additional Names: 2'-tert-butyl-5-methyl-2'-(3,5-xyloyl)chromane-6-carboh...
Literature References: Diacylhydrazine ecdysone mimetic for use in food crops. Prepn: M. Yanagi et al., EP 496342; eidem, US 5378726 (1992, 1995 both to Nippon Kayaku; Sankyo). Properties and biological activity: M. Yanagi et al., BCPC Conf. - Pests Dis. 2000, 27. Field trial against apple tortix: R. Ichinose et al., Annu. Rep. Sankyo Res. Lab. 52, 59 (2000). Mode of action: T. Toya et al., Biochem. Biophys. Res. Commun. 292, 1087 (2002). Series of articles on design, synthesis, and activity: Y. Sawada et al., Pest Manage. Sci. 59, 25-57 (2003). Review of development, environmental chemistry, safety, and toxicity: K. Tanaka et al., Annu. Rep. Sankyo Res. Lab. 53, 1-49 (2001).
CAS Name: 1,2-Benzenedicarboxylic acid bis(2-ethylhexyl) ester
Additional Names: bis(2-ethylhexyl) phthalate; di(2-ethylhexyl) phthalate; DOP; dioctyl phthalate
Trademarks: Octoil
Percent...
Literature References: Dialkyl phthalate ester plasticizer used to impart softness and flexiblilty to PVC products. Prepn: P. J. Garner, G. Watson, US 2508911 (1950 to Shell). Effect on dynamic mechanical properties: D. L. Hertz, Jr., Elastomerics 116, 20 (1984); interaction with PVC polymer: B. Garnaik, S. Sivaram, Macromolecules 29, 185 (1996). HPLC determn in PVC packaging: M. F. Aignasse et al., Int. J. Pharm. 113, 241 (1995). GC/MS determn in toys: R. Stringer et al., Environ. Sci. Pollut. Res. Int. 7, 27 (2000). Evaluation of carcinogenic risk: J. Doull et al., Regul. Toxicol. Pharmacol. 29, 327 (1999); of health effects: M. Fay et al., Toxicol. Ind. Health 15, 651 (1999). Review: L. G. Krauskopf, Plast. Compd. 6, 28-38 (1983). Review of environmental fate: C. A. Staples et al., Chemosphere 35, 667-749 (1997); of aquatic toxicity: idem et al., Environ. Toxicol. Chem. 16, 875 (1997); of toxicology and human exposure: Toxicological Profile for Di(2-ethylhexyl)phthalate (PB2003-100138, 2002) 337 pp.
CAS Name: 1,2-Benzenedicarboxylic acid diisononyl ester
Additional Names: diisononyl phthalate
Percent Composition: C 74.60%, H 10.11%, O 15.29%
Literature References: Dialkyl phthalate ester plasticizer used to impart softness and flexiblilty to PVC products. Prepn: P. J. Garner, G. Watson, US 2508911 (1950 to Shell). Effects on behavior and properties of PVC: S. V. Patel, M. Gilbert, Plast. Rubber Process. Appl. 6, 321 (1986); eidem, ibid. 8, 215 (1987). Effects of temperature on viscosity and density: L. D. Lorenzi et al., J. Chem. Eng. Data 43, 183 (1998). GC/MS determn in toys: R. Stringer et al., Environ. Sci. Pollut. Res. Int. 7, 27 (2000). Review: L. G. Krauskopf, Plast. Compd. 6, 28-38 (1983). Review of environmental fate: C. A. Staples et al., Chemosphere 35, 667-749 (1997). Review of health effects and risk assessment: C. F. Wilkinson, J. C. Lamb, Regul. Toxicol. Pharmacol. 30, 140-155 (1999); and environmental fate and toxicology: U. S. Gill et al., Rev. Environ. Contam. Toxicol. 172, 87-127 (2001).
CAS Name: 1,6-Dibromo-1,6-dideoxygalactitol
Additional Names: 1,6-dibromo-1,6-dideoxydulcitol; dibromodulcitol; dibromodulcit; DBDTrademarks: Elobromol (Chinoin)
Percent Composition: C 23.40...
Literature References: Diastereoisomer of mitobronitol, q.v., with myelosuppressive effects. Prepn and anticancer activity: NL 6600395; P. Horváth-Lengyel et al., US 3993781 (1966, 1976 both to Chinoin); B. Kellner et al., Nature 213, 402 (1967). Structure-activity correlations: L. Institoris et al., Arzneim.-Forsch. 17, 145 (1967). Pharmacological study: T. H. Corbett et al., Cancer 40, Suppl. 5, 2660 (1977). Metabolism, pharmacokinetics: I. P. Horváth et al., Eur. J. Cancer 15, 337 (1979). Clinical studies: W. Medina, J. M. Kirkwood, Cancer Treat. Rep. 66, 195 (1982); D. C. Tormey et al., Am. J. Clin. Oncol. 5, 33 (1982).
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