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.
Ammeline (4,6-diamino-2-hydroxy-1,3,5-triazine) is a triazine derivative.
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. Lower Explosive Limit (LEL): data unavailableAutoignition Temperature: data unavailable (NTP, 1992) Substance Min / Max listed below.
Substituierte s‐Triazine: Synthese und Reaktionen von 6‐Hydroxy‐2.4‐bis‐nitramino‐s‐triazin
Ammeline can be synthesized by the pyrolysis of urea or the condensation reaction among 2 moles of dicyandiamide and 1 mole of biuret. Molecular Formula.
C 3 Cl 2 N 3 NaO. EU. known to react with the
Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. HEXAHYDRO-1,3,5-TRIS(HYDROXYETHYL)-5-TRIAZINE is an amine and an alcohol. (NTP, 1992) Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. Enquire Now! Synonyms. It is the hydrolysis product of melamine.
It was not genotoxic and did not cause reproductive effects.
2-Sodium-hydroxy-4,6-dichloro-1,3,5-triazine .
Amines are chemical bases. They neutralize acids to form salts plus water.
Commercial. 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. SMALL SPILLS AND LEAKAGE: If you should spill this chemical, use absorbent paper to pick up all liquid spill material. 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.
Seal the absorbent paper, as well as any of your clothing which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Williamson ether synthesis is the benzylation of hydroxyl groups under basic conditions. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
More info about absorbents, including situations to watch out for...Belongs to the Following Reactive Group(s)Upper Explosive Limit (UEL): data unavailable Amines are chemical bases.
in the field of peptides and fibres. 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. Vapor Density (Relative to Air): data unavailable
These acid-base reactions are exothermic. Triazine-type hydroxy-group protecting agents. Notification.
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.
The dermal absorption of the ingredient was very low.
Synthesis. This section provides a listing of alternate names for this chemical,
Wash any surfaces you may have contaminated with a strong soap and water solution. including trade names and synonyms.