Conditions | Yield |
---|---|
Stage #1: urea at 140 - 160℃; under 6000.48 Torr; Stage #2: With ammonia; γ-Al2O3 under 750.06 - 1500.12 Torr; | 98% |
In water Product distribution / selectivity; | 88.5% |
With ammonia High Pressure; 70 to 300 at; at 350°C; 120 min; | 12.6% |
sodium cyanamide
A
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
In neat (no solvent) at 201.9℃; under 0.0008 Torr; for 18h; | A n/a B 98% |
Conditions | Yield |
---|---|
High Pressure; heating of equiv. amts. of dicyanodiamide and liquid NH3 in autoclave at 160°C at a pressure of 200 at; | 98% |
In further solvent(s) heating in isobutanol; | |
High Pressure; using Sn-Mg alloy for absorption of heat of reactn.; | <59 |
1,3,5-tribenzyl-2,4,6-triimino-1,3,5-triazine
hydrogen
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
With trimethyleneglycol In ethanol redn.; | 94% |
Conditions | Yield |
---|---|
With potassium hydroxide In water; dimethyl sulfoxide | 93% |
dicyandiamide
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
With ammonia High Pressure; at degree of charge of autoclave = 100%; yield depends on degree of charge of autoclave as follows: 44, 52, 77, 88.5 and 92% at degree of charge of 8, 17, 33, 67 and 100% respectively; | 92% |
In further solvent(s) heating in benzylamine; | 71% |
normal and higher pressure, above melting point; |
5-aminotetrazole
N-Cyanoguanidine
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
With hydrogenchloride In water at 100℃; for 24h; Time; Temperature; | 53% |
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
High Pressure; at 300°C; at a pressure of 40 at; 260 min; | 36.7% |
2-amino-4,6-diureido-1,3,5-triazine
A
2,4,6-triamino-s-triazine
B
ammeline
Conditions | Yield |
---|---|
With alkaline hydrolysis | A 33% B 9% |
Conditions | Yield |
---|---|
thermal decompn. in closed ampul; at 400°C; 180 min; | A 25% B 18% |
Conditions | Yield |
---|---|
High Pressure; at molar ratio of NH3:CS2 = 2:1; at 300°C; pressure = 40-90 at; 150 min; | 10.5% |
Conditions | Yield |
---|---|
thermal decompn. in closed ampul; at 200°C; 180 min; | A 4% B 4% |
thermal decompn. in closed ampul; at 200°C; 60 min; | A 3% B 3% |
Conditions | Yield |
---|---|
With chromium(III) oxide; ammonia at 450 - 750℃; oder anderen Katalysatoren; | |
With chromium(III) oxide; ammonia at 350 - 400℃; under 35 Torr; oder anderen Katalysatoren; | |
With ammonia; Cu-V-Ag-Pr-Co-Li/SiO2 at 380 - 400℃; under 760.051 - 37503.8 Torr; Product distribution / selectivity; | 0.18% |
Conditions | Yield |
---|---|
With ammonia at 100℃; | |
With ammonia at 450℃; | |
With ammonia 100-250°C, under pressure, in excess of NH3; | |
With ammonia 100-250°C, under pressure, in excess of NH3; |
cyanuric bromide
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
With ammonia beim Erwaermen unter Druck; | |
With ammonia 100-250°C, under pressure, excess waterfree NH3; | |
With ammonia beim Erwaermen unter Druck; | |
With ammonia 100-250°C, under pressure, excess waterfree NH3; |
Conditions | Yield |
---|---|
With ammonia at 180℃; |
Conditions | Yield |
---|---|
With ammonia at 300℃; |
Conditions | Yield |
---|---|
With ammonia; water at 150℃; |
Conditions | Yield |
---|---|
bei 150grad geht in Dicyandiamid ueber, das bei hoeherem Erhitzen in Melamin und Ammoniak zerfaellt; | |
With acids | |
heating over 110°C; |
Conditions | Yield |
---|---|
With ammonia at 170 - 180℃; |
Conditions | Yield |
---|---|
at 250℃; rhodanwasserstoffsaeures Melamin entsteht; |
Conditions | Yield |
---|---|
With water; phenol at 100℃; zuletzt Erhitzen auf 160grad; | |
With ammonia at 160℃; | |
at 180 - 190℃; | |
With ammonia In water byproducts: CO2; heating at 160°C in closed tube; | |
With NH3 In water byproducts: CO2; heating at 160°C in closed tube; |
Conditions | Yield |
---|---|
at 140 - 175℃; |
ethanol
Diethylcyanamide
guanidine hydrobromide
guanidine nitrate
A
2,4,6-triamino-s-triazine
B
N,N-diethylimidodicarbonimidic diamide
Conditions | Yield |
---|---|
at 100℃; |
Conditions | Yield |
---|---|
unter Druck; |
guanidine nitrate
N-Cyanoguanidine
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
With hydrogenchloride at 180 - 250℃; | |
unter Druck; |
Conditions | Yield |
---|---|
at 400 - 450℃; under 152000 Torr; |
Conditions | Yield |
---|---|
With hydrogenchloride at 180 - 250℃; | |
byproducts: NH3; heating at 160°C; |
Conditions | Yield |
---|---|
unter Druck; |
Conditions | Yield |
---|---|
In benzene for 5h; Reflux; | 100% |
With acetic acid In N,N-dimethyl-formamide for 6h; Reflux; | 73% |
In benzene Reflux; | 72% |
In neat (no solvent) Heating; | |
In benzene |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid at 290℃; for 2h; Product distribution / selectivity; | 100% |
at 339.84 - 359.84℃; for 48h; Pyrolysis; | |
at 335℃; | |
Stage #1: 2,4,6-triamino-s-triazine With ammonium chloride at 449.84℃; for 12h; Sealed tube; Stage #2: With ammonium hydroxide at 199.84℃; for 12h; |
2,4,6-triamino-s-triazine
tribromomelamine
Conditions | Yield |
---|---|
With sodium hydroxide; bromine In water at 20℃; for 2.16667h; | 100% |
With bromine; sodium hydroxide In water at 20℃; | |
With bromine; sodium hydroxide In water |
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
With phosphoric acid; zinc(II) oxide In water at 70 - 80℃; Temperature; Large scale; | 100% |
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
In water | 100% |
p-chlorodibenzo[c.e][1,2]oxaphosphorine
2,4,6-triamino-s-triazine
Conditions | Yield |
---|---|
With 1-methyl-1H-imidazole at 100℃; for 16h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
In acetonitrile Cu compd. dissolved in Ar-degassed MeCN, melamine added, suspn. sealed in glass tube, heated with stirring to 100°C for 14 h; filtered, washed with MeCN and Et2O, dried in vac.; elem. anal.; | 99.6% |
2,4,6-triamino-s-triazine
cyanuric acid melamine
Conditions | Yield |
---|---|
Stage #1: isocyanuric acid for 0.166667h; Stage #2: 2,4,6-triamino-s-triazine With K-SMA In water at 95 - 120℃; for 5h; Product distribution / selectivity; Heating / reflux; | 99.5% |
Stage #1: isocyanuric acid In water at 20℃; for 0.166667 - 30h; Stage #2: 2,4,6-triamino-s-triazine In water at 100℃; for 4h; Product distribution / selectivity; |
2,4,6-triamino-s-triazine
4-amino-1-hydroxybutylidenebisphosphonic acid
Conditions | Yield |
---|---|
With water pH=Ca. 6 - 8; Heating; | 99% |
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 180℃; for 40h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
In water at 85℃; for 4h; Temperature; Solvent; | 99% |
Conditions | Yield |
---|---|
In ethanol; water at 75℃; for 2h; Solvent; Temperature; | 99% |
Conditions | Yield |
---|---|
In water at 72℃; for 5h; | 99% |
Conditions | Yield |
---|---|
In ethanol at 75℃; for 5h; Temperature; Solvent; | 99% |
2,4,6-triamino-s-triazine
nitrogen
boric acid
boron nitride
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) byproducts: NH3, H2O, NO2; mixt. of powders C3N6H6:H3BO3 of molar ratio 1:2.25 (loaded on graphite boats) treated in intermediate-frequency furnace (300-1000 Hz) at temp. of 1800-1950°C under N2 flow rate of 5-8 l/min; detd. by XRD, SEM; | 98.54% |
Melamine has the IUPAC name of 1,3,5-Triazine-2,4,6-triamine. Melamine is white solid with the formula C3H6N6. Melamine is soluble in water, glycol, glycerin and pyridine; slightly soluble in ethanol; insoluble in diethyl ether, benzene and carbon tetrachloride. In addition, Melamine is incompatible with strong oxidizing agents and strong acids. Melamine will sublime when gently heated. It has the CAS register number of 108-78-1 and EINECS register number of 203-615-4. What's more, you should protect Melamine from moisture, heat, ignition sources, and incompatible substances. On the other hand, Melamine should be protected from direct light.
Preparation: You can use urea to produce Melamine as the following reaction which is very common in most industrial manufacturers. This reaction can be carried out by either of two methods: catalyzed gas-phase production or high pressure liquid-phase production. Currently, China is the world's largest exporter of melamine, while its domestic consumption still grows by 10% per year.
6 (NH2)2CO → C3H6N6 + 6 NH3 + 3 CO2
Melamine can also be prepared by dicyandiamide and ammonia in solvent of methanol at temperature of 200 °C. Per ton of product will consume 1180Kg dicyandiamide (98% ), 30 Kg liquid ammonia in this method.
H4C2N4 + NH3 [CH3OH] → C3H6N6
Uses: Both the Melamine and formaldehyde can be used to produce melamine resin which is a very durable thermosetting plastic used in Formica, and Melamine foam, a polymeric cleaning product. As superplasticizer, Melamine can also enter the fabrication of Melamine poly-sulfonate for making high-resistance concrete. As fertilizer, Melamine had been envisaged for crops because of its high nitrogen content. However, Melamine is much more expensive to produce than other common nitrogen fertilizers, such as urea. Melamine and its salts are used as fire-retardant additives in paints, plastics and paper. Melamine is sometimes illegally added to food products in order to increase the apparent protein content.
Regulation: The United Nations' food standards body, Codex Alimentarius Commission, has set the maximum amount of Melamine allowed in powdered infant formula to 1 mg/kg and the amount of Melamine allowed in other foods and animal feed to 2.5 mg/kg. While not legally binding, the levels allow countries to ban importation of products with excessive levels of melamine.
When using the Melamine, you should be very cautious because it is irritant and harmful. Melamine is harmful by inhalation and in contact with skin. Melamine may cause sensitisation by skin contact. There will be a risk of explosion if heated Melamine under confinement. Whenever you will use Melamine, you should wear suitable protective clothing and gloves.
Descriptors computed from structure of Melamine:
(1)Canonical SMILES: C1(=NC(=NC(=N1)N)N)N
(2)InChI: InChI=1S/C3H6N6/c4-1-7-2(5)9-3(6)8-1/h(H6,4,5,6,7,8,9)
(3)InChIKey: JDSHMPZPIAZGSV-UHFFFAOYSA-N
Toxicity of Melamine:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | oral | 3296mg/kg (3296mg/kg) | Toxicology and Applied Pharmacology. Vol. 72, Pg. 292, 1984. | |
mouse | LD50 | unreported | 1gm/kg (1000mg/kg) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 58(2), Pg. 14, 1993. | |
mouse | LDLo | intraperitoneal | 800mg/kg (800mg/kg) | SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE BEHAVIORAL: TREMOR LUNGS, THORAX, OR RESPIRATION: CYANOSIS | "Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2A, Pg. 2769, 1981. |
rabbit | LD50 | skin | > 1gm/kg (1000mg/kg) | Acute Toxicity Data. Journal of the American College of Toxicology, Part B. Vol. 1, Pg. 110, 1990. | |
rat | LC50 | inhalation | 3248mg/m3 (3248mg/m3) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 58(2), Pg. 14, 1993. | |
rat | LD50 | oral | 3161mg/kg (3161mg/kg) | Toxicology and Applied Pharmacology. Vol. 72, Pg. 292, 1984. | |
rat | LD50 | unreported | 6gm/kg (6000mg/kg) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 58(2), Pg. 14, 1993. | |
rat | LDLo | intraperitoneal | 3200mg/kg (3200mg/kg) | SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE BEHAVIORAL: TREMOR LUNGS, THORAX, OR RESPIRATION: CYANOSIS | "Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2A, Pg. 2769, 1981. |
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