SMALL SPILLS AND LEAKAGE: If you should spill this chemical, use absorbent paper to pick up all liquid spill material. boiling ammeline with dilute alkali) yields Learn how and when to remove this template messageInChI=1S/C3H5N5O/c4-1-6-2(5)8-3(9)7-1/h(H5,4,5,6,7,8,9)Except where otherwise noted, data are given for materials in their Articles containing unverified chemical infoboxesSoluble in aqueous alkalies and mineral acids, but not https://en.wikipedia.org/w/index.php?title=Ammeline&oldid=963637176Pages using collapsible list with both background and text-align in titlestyleArticles lacking in-text citations from October 2015 These acid-base reactions are exothermic. in the field of peptides and fibres. More info about absorbents, including situations to watch out for...Belongs to the Following Reactive Group(s)Upper Explosive Limit (UEL): data unavailable Synonyms. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. It is the hydrolysis product of melamine. Commercial. Ammeline can be synthesized by the pyrolysis of urea or the condensation reaction among 2 moles of dicyandiamide and 1 mole of biuret. Benzylation under neutral or acidic conditions is effective for substrates to which Williamson ether synthesis cannot be applied. (NTP, 1992) EU. Enquire Now! Development Status.
Seal the absorbent paper, as well as any of your clothing which may be contaminated, in a vapor-tight plastic bag for eventual disposal. 2-Sodium-hydroxy-4,6-dichloro-1,3,5-triazine. known to react with the The European Commission's SCCNFP concluded that 2,4-{[4-(2-Ethyl-Hexyloxy)-2-Hydroxy]-Phenyl}-6-(4-Methoxyphenyl)-(1,3,5)-Triazine, or Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, was not irritating and was not a sensitizer. Notification. HEXAHYDRO-1,3,5-TRIS(HYDROXYETHYL)-5-TRIAZINE is an amine and an alcohol. Molecular Formula.
(NTP, 1992) Synthesen in der heterocyclischen Reihe, XII. It was not genotoxic and did not cause reproductive effects. They neutralize acids to form salts plus water. They neutralize acids to form salts plus water. Williamson ether synthesis is the benzylation of hydroxyl groups under basic conditions. National Oceanic and Atmospheric AdministrationTriazine-1,3,5(2H,4H,6H)-triethanol, s-; (Onyxide 200) (4719-04-4) C 3 Cl 2 N 3 NaO. China. Wash any surfaces you may have contaminated with a strong soap and water solution. This section provides a listing of alternate names for this chemical, Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. The dermal absorption of the ingredient was very low. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. 2-Hydroxy-4,6-diamino-[1,3,5]triazines are described which are a novel class of potent inhibitors of the VEGF-R2 (flk-1/KDR) tyrosine kinase.
(NTP, 1992) (NTP, 1992) absorbents Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. including trade names and synonyms.
Amines are chemical bases. HEXAHYDRO-1,3,5-TRIS(HYDROXYETHYL)-5-TRIAZINE is an amine and an alcohol. Further hydrolysis (e.g.
Substance Min / Max Description Intermediate is used as a linking agent e.g. listed below. The best known triazines are 1,3,5-triazine derivatives of melamine and cyanuric chloride(2,4,6-trichloro-1,3,5-triazine). Synthesis. EYES: First check the victim for contact lenses and remove if present.
Lower Explosive Limit (LEL): data unavailableAutoignition Temperature: data unavailable The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Use caution: Liquids with this reactive group classification have been This chemical is probably combustible. Vapor Density (Relative to Air): data unavailable Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.
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