4719-04-4 Usage
Description
Hexahydro-1,3,5-tris(hydroxyethyl)-s-triazine, also known as Grotan BK, is a triazine derivative that exists as a light yellow solid. It is characterized by its viscous yellow liquid form and is commonly used in various applications due to its unique chemical properties.
Uses
Used in Organic Synthesis:
Hexahydro-1,3,5-tris(hydroxyethyl)-s-triazine is used as an intermediate in the synthesis of various organic compounds, contributing to the development of new chemical products and materials.
Used in Cooling Fluids:
In the industry of cutting fluids, Hexahydro-1,3,5-tris(hydroxyethyl)-s-triazine is used as a formaldehyde releaser, which helps to improve the performance and longevity of the fluids, ensuring efficient and safe cutting processes.
Used as a Bactericide:
Hexahydro-1,3,5-tris(hydroxyethyl)-s-triazine is utilized as a bactericide in various applications, including cooling fluids and cosmetic products. Its antimicrobial properties help to prevent the growth of harmful microorganisms, ensuring the safety and efficacy of these products.
Used in Cosmetic Products:
Hexahydro-1,3,5-tris(hydroxyethyl)-s-triazine is used as a preservative in the cosmetic industry to maintain the freshness and quality of products by inhibiting the growth of bacteria and other microorganisms.
Air & Water Reactions
Water soluble.
Reactivity Profile
Hexahydro-1,3,5-tris(hydroxyethyl)-s-triazine is an amine and an alcohol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. 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. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.
Fire Hazard
Hexahydro-1,3,5-tris(hydroxyethyl)-s-triazine is probably combustible.
Flammability and Explosibility
Notclassified
Contact allergens
Grotan BK is a triazine derivative contained as a bio cide in cutting fluids. It is a formaldehyde releaser.
Dermatitis, delayed-type allergic conjunctivitis, and
asthma were described.
Check Digit Verification of cas no
The CAS Registry Mumber 4719-04-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,1 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4719-04:
(6*4)+(5*7)+(4*1)+(3*9)+(2*0)+(1*4)=94
94 % 10 = 4
So 4719-04-4 is a valid CAS Registry Number.
4719-04-4Relevant articles and documents
Regioselective synthesis of 1,5-Diaryl-2-(Hydroxyalkyl)-8-Methylglycolurils
Antonova,Baranov,Nelyubina,Kravchenko
, p. 503 - 513 (2014)
The cyclocondensation of N-methylurea with derivatives of tetrahydroimidazooxazolone, tetrahydro-imidazooxazinone, dihydroimidazooxazinone, and tetrahydroimidazooxazepinone was studied for the first time. It was shown that the reactions take place with high regioselectivity, are regular in character, and lead to the formation of previously inaccessible 1,5-diaryl-2-(hydroxyalkyl)-8-methylglycolurils with high yields.
HEXAHYDROTRIAZINES, SYNTHESIS AND USE
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Paragraph 0021, (2013/05/23)
Methods for making asymmetrical triazines are provided. The methods comprise first forming a mixture of at least two primary amines then reacting the mixture with an aldehyde. Methods for removing sulfides from hydrocarbon streams are also provided. The triazines may be added to the hydrocarbon stream in a molar ratio of triazine:H2S of about 10:1 to about 1:2 wherein R1, R2, and R3 are chosen from alkyls, hydroxyl-substituted alkyls, and alkoxy-substituted alkyl of 1 to 10 carbon atoms, with the proviso that R1, R2, and R3 are not all the same.
2-(1,3,5-Dithiazinan-5-yl)ethanol heterocycles, structure and reactivity
Gálvez-Ruiz, Juan Carlos,Jaen-Gaspar, Javier C.,Castellanos-Arzola, Indira G.,Contreras, Rosalinda,Flores-Parra, Angelina
, p. 2269 - 2285 (2007/10/03)
Treatment of 2-(1,3,5-dithiazinan-5-yl)ethanol (1), 2-(1,3,5-dithiazinan-5- yl)-1-phenylethanol (2), 2-(1,3,5-dithiazinan-5-yl)-1-methylethanol (3) and 2-(1,3,5-dithiazinan-5-yl)-2-methyl-1-phenylethanol (4) with TsCl and NEt 3 in CH2Cl2 afforded the corresponding 3-tosyl-1,3-oxazolidine derivatives (5-8), whereas tosylation of 1-4 in the presence of NHMe3Cl gave the corresponding O-tosyl-2-(1,3,5- dithiazinan-5-yl)ethanol derivatives (11-14). The direct preparation of 5 and 7 from formaldehyde and N-tosylethanolamine (9) or N-tosyl-2-propanolamine was not successful. Reactions of 1 or 3 with benzylamine furnish 1,3,5-tribenzyl-1,3,5- triazinane. Heating of 1 and 2 affords the corresponding 1,3,5-tri(2- hydroxyethyl)-1,3,5-triazinanes. X-Ray diffraction studies of compounds (1-9 and 11) are reported.