They neutralize acids to form salts plus water. 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. Ammeline can be synthesized by the pyrolysis of urea or the condensation reaction among 2 moles of dicyandiamide and 1 mole of biuret.
IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. They neutralize acids to form salts plus water.
Description Intermediate is used as a linking agent e.g. 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. Commercial. Further hydrolysis (e.g. These acid-base reactions are exothermic. including trade names and synonyms. Amines are chemical bases.
Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. EU. This section provides a listing of alternate names for this chemical, Seal the absorbent paper, as well as any of your clothing which may be contaminated, in a vapor-tight plastic bag for eventual disposal. More info about absorbents, including situations to watch out for...Belongs to the Following Reactive Group(s)Upper Explosive Limit (UEL): data unavailable
absorbents US. Synonyms. (NTP, 1992) (NTP, 1992)
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 Vapor Density (Relative to Air): data unavailable 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. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center.
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. Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. Ammeline (4,6-diamino-2-hydroxy-1,3,5-triazine) is a triazine derivative. Triazine-type hydroxy-group protecting agents. Lower Explosive Limit (LEL): data unavailableAutoignition Temperature: data unavailable National Oceanic and Atmospheric AdministrationTriazine-1,3,5(2H,4H,6H)-triethanol, s-; (Onyxide 200) (4719-04-4) Substance Min / Max EYES: First check the victim for contact lenses and remove if present. 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. Specification. HEXAHYDRO-1,3,5-TRIS(HYDROXYETHYL)-5-TRIAZINE is an amine and an alcohol. 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. Use caution: Liquids with this reactive group classification have been
Substituierte s‐Triazine: Synthese und Reaktionen von 6‐Hydroxy‐2.4‐bis‐nitramino‐s‐triazin Wash any surfaces you may have contaminated with a strong soap and water solution. Triazine is a class of nitrogen-containing heterocycles. PHYSICAL DESCRIPTION: Viscous yellow liquid. Benzylation under neutral or acidic conditions is effective for substrates to which Williamson ether synthesis cannot be applied. Williamson ether synthesis is the benzylation of hydroxyl groups under basic conditions.