Detail of "6606-65-1"

CAS Number:
6606-65-1
Name:
Enbucrilate
Molecular Structure:
Formula:
C₈H₁₁NO₂
Molecular Weight:
153.17844
Synonyms:
Acrylicacid, 2-cyano-, butyl ester (6CI,7CI,8CI);BK 201 (adhesive);BK 301 (adhesive);Butyl 2-cyanoacrylate;Butyl cyanoacrylate;Butyl a-cyanoacrylate;Histacryl Blue;Indermil;InteguSeal Clear;Integuseal;Integuseal MicrobialSealant;Sicomet 6000;Tisuacryl;n-Butyl 2-cyanoacrylate;
EINECS:
229-552-2
Density:
1.005 g/cm³
Boiling Point:
232.8 °C at 760 mmHg
Flash Point:
100.6 °C

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Assay:99% Package:200kg/b

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n-Butyl cyanoacrylate

560 Integral
560

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Supplier:Amadis Chemical Co., Ltd. [ China (Mainland)]

600 Integral
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Termination and transfer by acids in the pyridine-initiated polymerization of butyl cyanoacrylate: Termination and transfer by acids in the pyridine-initiated polymerization of butyl cyanoacrylate. Costa, G.; Cronin, J. P.; Pepper, D. C.; Loonan, C. (Chem. Lab., Trinity Coll., Dublin, Ire.). Eur. Polym. J., 19(10-11), 939-45 (English) 1983. CODEN: EUPJAG. ISSN: 0014-3057. DOCUMENT TYPE: Journal CA Section: 35 (Chemistry of Synthetic High Polymers) H2SO4, CF3SO3H [1493-13-6], p-MeC6H4SO3H [104-15-4], and HCl caused identical inhibition periods in the polymn. of Bu cyanoacrylate [6606-65-1] by pyridine in THF at 20°; CF3COOH [76-05-1] caused less sharply defined inhibition, and ClCH2COOH [79-11-8] retarded. This confirmed earlier measurements and the composite initiation rate const. for pyridine. The rates of monomer consumption during inhibition gave ratios of acid termination to propagation rate consts., which ranged 20-fold from H2SO4 to CF3COOH. The effect on mol. wt. was independent of acid type, and results from rapid transfer by the terminal acid proton of killed oligomer and polymer mols.

Production of a curative preparation of prednisolone F and butyl 2-cyanoacrylate for dental purposes: Production of a curative preparation of prednisolone F and butyl 2-cyanoacrylate for dental purposes. Dimov, C.; Nowakov, P.; Issaev, I.; Spiridonova, D. (Med. Inst., Pharm. Fac., Sofia, Bulg.). Pharmazie, 32(5), 286 (German) 1977. CODEN: PHARAT. DOCUMENT TYPE: Journal CA Section: 63 (Pharmaceuticals) A stable therapeutically active prednisolone F [50-02-2] compn. was prepd. by dispersing perdnisolone F in Et2O [60-29-7] and adding Bu 2-cyanoacrylate [6606-65-1] to the suspension. The Et2O was evapd. at room temp., and the homogenous suspension was placed into ampuls and kept for 6 months in the dark at 10.degree.. Sedimentation tests indicated good stability of the prepn. The compn. can be used in the treatment of mouth and gum ailments and mucous membrane disorders. A suspension of prednisolone F in Bu 2-cyanoacrylate was unstable and still contained prednisolone F 48 h after application to the mucous membrane.