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Busan 1060 is a triazine derivative contained in cutting fluids.
Busan 1060 is a formaldehyde releaser.
Busan 1060 is a light-yellow liquid.
CAS: 4719-04-4
MF: C9H21N3O3
MW: 219.28
EINECS: 225-208-0
Synonyms
1,3,5-Tris(2-hydroxyethyl)hexahydro-1,3,5-triazine;1,3,5-triazine-1,3,5(2h,4h,6h)-triethanol;HEXAHYDRO-1,3,5-TRIS(2-HYDROXYETHYL)-TRIAZINE;HEXAHYDRO-1,3,5-TRIS(HYDROXYETHYL)-S-TRIAZINE;HEXAHYDRO-1,3,5-TRIS(HYDROXYETHYL)TRIAZINE;2,2’,2’’-(hexahydro-1,3,5-triazine-1,3,5-triyl)triethanol;Triethanol = Hexahydro - 1,3,5, - Tri - Hydroxyethyl - S-Triazine;s-Triazine-1,3,5-triethanol
Busan 1060 is a formaldehyde condensate product that is used as an antimicrobial agent in metal working fluids.
Busan 1060 is a chemical compound that belongs to the class of s-triazines.
Busan 1060 is synthesized from fatty acids and potassium dichromate.
Busan 1060 has been shown to have microbicidal activity against bacteria such as Escherichia coli and Staphylococcus aureus.
Busan 1060 also has anti-inflammatory effects by inhibiting leukotriene synthesis and blocking leukotriene receptor antagonists.
This drug has been shown to cause allergic reactions in humans and may be carcinogenic in animals.
Busan 1060 is not known what the environmental effects of this substance are because it has not been tested for toxicity or bioaccumulation in aquatic organisms.
Busan 1060 may be used as an additive in animal feed because it increases the growth rate of livestock when included at low concentrations.
Busan 1060 is a reliable storage tank-side antimicrobial chemical.
People usually put Busan 1060 directly into the sump of a badly fouled, high-smell system.
Busan 1060 works well against both gram-positive and also gram-negative microorganisms.
The effectiveness of Busan 1060 is not influenced by either the water hardness or various other chemicals.
This micro biocide can also boost the efficiency of the liquid.
As well as additionally manages fungal development and also prevents the growth of germs.
Busan 1060 Chemical Properties
Boiling point: 360.1°C (rough estimate)
Density: 1.1269 (rough estimate)
Vapor pressure: 0Pa at 25℃
Refractive index: 1.4830 (estimate)
Storage temp.: 2-8°C
Solubility: Ethyl Acetate (Slightly, Sonicated), Water (Slightly)
Form: Oil to Low-Melting Solid
pka: 14.16±0.10(Predicted)
Color: Off-White to Yellow
Water Solubility: Soluble (>=1 g/100 mL at 24 ºC)
InChI: InChI=1S/C9H21N3O3/c13-4-1-10-7-11(2-5-14)9-12(8-10)3-6-15/h13-15H,1-9H2
InChIKey: HUHGPYXAVBJSJV-UHFFFAOYSA-N
LogP: -2 at 24℃
CAS DataBase Reference: 4719-04-4(CAS DataBase Reference)
EPA Substance Registry System: Busan 1060 (4719-04-4)
Uses
Busan 1060 is used in organic synthesis; as a bactericide in cooling fluids and various cosmetic products; formaldehyde liberator.
1. Mainly used as anticorrosion for paper coatings, emulsified aqueous solutions and starch suspensions.
2. Busan 1060's effect has reached the level of SN-215 of similar foreign products.
3Busan 1060 has an inhibitory effect on bacteria commonly found in papermaking.
4. Add 250 kg/tof this productto the coated paper to have a good anti-fog effect.
Reactivity Profile
Busan 1060 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.
Synthesis
General procedure for the synthesis of hydroxyethyl hexahydrohomotriazine from formaldehyde and 2-aminoethanol: To 6.1 g (0.1 mol) of 2-aminoethanol was added 3.0 g (0.1 mol as formaldehyde) of a 20 mL methanol solution of paraformaldehyde, and the mixture was stirred for 48 h at room temperature.
Upon completion of the reaction, the solvent was removed by rotary evaporator and the residue was distilled under reduced pressure to give 6.3 g (86% yield) of light yellow viscous liquid.
The physicochemical properties of the obtained compound (I) were in accordance with the data reported in literature.
