Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. chemBlink provides information about CAS # 1075-59-8, 2-Hydroxy-4,6-dimethoxy-1,3,5-triazine, 4,6-Dimethoxy-1,3,5-triazin-2(1H)-one, Dimethyl cyanurate, molecular formula: C5H7N3O3. EYES: First check the victim for contact lenses and remove if present. With three amino substituents, melamine is a precursor to commercial resins. They neutralize acids to form salts plus water. Wash any surfaces you may have contaminated with a strong soap and water solution. Ammeline can be synthesized by the pyrolysis of urea or the condensation reaction among 2 moles of dicyandiamide and 1 mole of biuret. 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. US. Substituierte s‐Triazine: Synthese und Reaktionen von 6‐Hydroxy‐2.4‐bis‐nitramino‐s‐triazin Commercial. More info about absorbents, including situations to watch out for...Belongs to the Following Reactive Group(s)Upper Explosive Limit (UEL): data unavailable Lower Explosive Limit (LEL): data unavailableAutoignition Temperature: data unavailable C 3 Cl 2 N 3 NaO. 2-Sodium-hydroxy-4,6-dichloro-1,3,5-triazine . Buy 2,4-Bis(2-hydroxy-4-methoxyphenyl) -6-ethyl mercaptan-1,3,5-triazine (Appolo-124), (C19H19N3O4S) a pale yellow powder best and widely used as UV absorber additive in textile auxiliary. absorbents HEXAHYDRO-1,3,5-TRIS(HYDROXYETHYL)-5-TRIAZINE is an amine and an alcohol. These acid-base reactions are exothermic. Substance Min / Max known to react with the Enquire Now! Amines are chemical bases. Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. Specification. 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. 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. (NTP, 1992) 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. in the field of peptides and fibres. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. Synthesis. Further hydrolysis (e.g. Triazine is a class of nitrogen-containing heterocycles. (NTP, 1992) InChI=1/C3H5N5O/c4-1-6-2(5)8-3(9)7-1/h(H5,4,5,6,7,8,9)Creative Commons Attribution-ShareAlike LicenseAmmeline is the first step in melamine hydrolysis. These acid-base reactions are exothermic. SMALL SPILLS AND LEAKAGE: If you should spill this chemical, use absorbent paper to pick up all liquid spill material. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Vapor Density (Relative to Air): data unavailable Synonyms. HEXAHYDRO-1,3,5-TRIS(HYDROXYETHYL)-5-TRIAZINE is an amine and an alcohol. Use caution: Liquids with this reactive group classification have been Benzylation under neutral or acidic conditions is effective for substrates to which Williamson ether synthesis cannot be applied. Development Status. listed below. The dermal absorption of the ingredient was very low. It was not genotoxic and did not cause reproductive effects. 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. This section provides a listing of alternate names for this chemical, Amines are chemical bases. including trade names and synonyms. Notification. Triazine-type hydroxy-group protecting agents. EU. Description Intermediate is used as a linking agent e.g. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. This chemical is probably combustible. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. Williamson ether synthesis is the benzylation of hydroxyl groups under basic conditions. They neutralize acids to form salts plus water. (NTP, 1992) Synthesen in der heterocyclischen Reihe, XII. Molecular Formula. Ammeline (4,6-diamino-2-hydroxy-1,3,5-triazine) is a triazine derivative. National Oceanic and Atmospheric AdministrationTriazine-1,3,5(2H,4H,6H)-triethanol, s-; (Onyxide 200) (4719-04-4) It is the hydrolysis product of melamine. PHYSICAL DESCRIPTION: Viscous yellow liquid. (NTP, 1992) China. 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 The best known triazines are 1,3,5-triazine derivatives of melamine and cyanuric chloride(2,4,6-trichloro-1,3,5-triazine).

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