MoSSe

Ghahramani E, Moss D J and Sipe J E 1990 Second-harmonic generation in odd-period, strained, (Si)y(Ge) Si superlattices and at Si/Ge interfaces Phys. Rev. Lett. 64 2815-18... 

Sipe J E, Moss D J and van Driel H M 1987 Phenomenological theory of optical second- and third-harmonic generation from cubic centrosymmetric crystals Phys. Rev. B 35 1129-41... 

Dura J A, Pippenger P M, Flalas N J, Xiong X Z, Chow P C and Moss S C 1993 Epitaxial integration of single crystal Cgq Appi. Rhys. Lett. 63 3443-5... 

CHECK R Laskowski, M W MacArthur, D S Moss and J M Thornton 1993. Procheck - A program to check the stereochemical quality of protein structures. Journal of Applied Crystallography 26 283-291. 

Moss silver Mostat Series Mothproofing Mothproofing agents Motilin... 

This seaweed became known as Irish moss. The extraction and purification of the polysaccharide from Irish moss was patented in 1871 (29). This polysaccharide eventually became known as carrageenan it was not produced and marketed until 1937. 

Fougere Family. This family has a typically accepted masculine note reminiscent of fern, tonka, and moss. 

Outdoor Pests biting flies, fire ants, hornets, mosquitoes, ticks, wasps mice, moles snails, slugs mil dews, molds, mosses... 

Pu(N03 ) -5H2 0 deep red plutonyl nitrate hexahydrate [19125-90-7], Pu02(N03 )2-6H2 0 coral red anhydrous plutonium(IV) sulfate [13692-89-2], Pu(S0 2i pinh or redPu(S0 2 4H20 and moss green plutonyl carbonate/ P2P2-/(9-P/, PUO2CO2 (30). 

B. Moss, iu W. A. Carter, ed, Selectipe Inhibitors of Viral Functions, Chemical Rubber Co. Press, Qeveland, Ohio, 1973, p. 313. 

Composites A.n Insider s Technical Guide to Corporate America s Activities, Turner Moss Co., New York, 1989. 

Silver sulfide is exceptionally stable in air and sunlight, but decomposes when heated to 810°C. Moss silver (filiform silver), consisting of long hair-like growths of pure silver, is formed when silver sulfide is heated for a prolonged period at elevated temperatures below 810°C. 

In detergent perfumes, the stabiUty of vanillin is not always certain. It depends on the association made with other raw materials, eg, with patchouli, frankincense, cloves, most of the animal notes, and such chemicals as amyl saUcylate, methyl ionones, heflotropin, gamma undecalactone, linalool, methyl anthrarulate, benzyl acetate, phenyl ethyl alcohol, cedar wood derivatives, oak mosses, coumarin, benzoin. Pern balsam, and cistus derivatives. In some cases, these mixtures can cause discoloration effects. 

The use of high concentrations of vanillin in soap perfumery can cause discoloring effects over time, dark or black spots appear on the soap and foaming power is reduced. In some cases, however, the use of Rhodiarome ethylvanillin is possible, because ethylvanillin [121 -32-4] does not cause the same discoloration problems and, being at least three times more powerful than vanillin, can be used alone. Some surprising cases show that with oak or tree mosses and large amounts of methyl ionones, the soap perfume may look fine and have a low discoloration, and yet over time vanillin crystals can appear on the soap itself. 

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