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Sodium cyanate. C (#N) [O-]. [Na+] Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Sodium cyanate is the inorganic compound with the formula NaOCN. A white solid, it is the sodium salt of the cyanate anion.
INCI names often differ greatly from systematic chemical nomenclature or from more common trivial names and is a mixture of conventional scientific names, Latin and English words. INCI nomenclature conventions "are continually reviewed and modified when necessary to reflect changes in the industry, technology, and new ingredient developments". [2]
acidulant; skin peeler cocamide dea: CH 3 (CH 2) n C(=O)N(CH 2 CH 2 OH) 2, where n is from 8 to 18 foaming and/or emulsifying agent cyclohexasiloxane: Dodecamethylcyclohexasiloxane (D6) solvent cyclopentasiloxane (a type of silicone) [citation needed] Decamethylcyclopentasiloxane (D5) solvent cetyl alcohol: CH 3 (CH 2) 15 OH various calcium ...
Cyanide is a potent cytochrome c oxidase (COX, a.k.a. Complex IV) inhibitor, causing asphyxiation of cells. As such, cyanide poisoning is a form of histotoxic hypoxia, because it interferes with the ability of cells to take or use oxygen via oxidative phosphorylation. [ 25 ]: 1475. Specifically, cyanide binds to the heme a3-CuB binuclear center ...
Cyanoacrylate glue is widely used in human and veterinary medicine.[6] It was in veterinary use for mending bone, hide, and tortoise shell by the early 1970s or before. A cyanoacrylate spray was used in the Vietnam Warto reduce bleeding in wounded soldiers until they could be taken to a hospital.
Cyanate ester. Cyanate esters are chemical compounds in which the hydrogen atom of the cyanic acid is replaced by an organyl group (for example aryl group). The resulting compound is termed a cyanate ester, with the formula R−O−C≡N, where R is an organyl group. Cyanate esters contain a monovalent cyanate group −O−C≡N.
Sodium cyanide is a poisonous compound with the formula Na C N. It is a white, water-soluble solid. Cyanide has a high affinity for metals, which leads to the high toxicity of this salt. Its main application, in gold mining, also exploits its high reactivity toward metals. It is a moderately strong base.
structure summary. The enzyme cyanase (EC 4.2.1.104, also known as cyanate hydratase or cyanate lyase), catalyses the bicarbonate dependent metabolism of cyanate to produce ammonia and carbon dioxide. [1][2] The systematic name of this enzyme is carbamate hydrolyase. In E. coli, cyanase is an inducible enzyme and is encoded for by the cynS gene ...