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645-05-6

645-05-6 Structure

645-05-6 Structure
IdentificationMore
[Name]

Altretamine
[CAS]

645-05-6
[Synonyms]

2,4,6-TRIS(DIMETHYLAMINO)-1,3,5-TRIAZINE
ALTRETAMIN
ALTRETAMINE
HEXAMETHYLMELAMINE
N,N,N',N',N'',N''-HEXAMETHYL-1,3,5-TRIAZINE-2,4,6-TRIAMINE
1,3,5-Triazine-2,4,6-triamine, N,N,N',N',N'',N''-hexamethyl-
1,3,5-tris(dimethylamino)-s-triazine
2,4,6-tris(dimethylamino)-s-triazin
2,4,6-Tris(Dimethylamino)-s-triazine
5-triazine-2,4,6-triamine,n,n,n’,n’,n’’,n’’-hexamethyl-3
Aitretamine
ENT 50852
ENT050852
ent50852
Hemel
Hexalen
hexamethyl-melamin
Hexastat
HMM
HTM
[EINECS(EC#)]

211-428-4
[Molecular Formula]

C9H18N6
[MDL Number]

MFCD00549245
[Molecular Weight]

210.28
[MOL File]

645-05-6.mol
Chemical PropertiesBack Directory
[Definition]

A hexamethyl-2,4,6- triamine derivative of 1,3,5-triazine.
[Melting point ]

171-175 °C (lit.)
[Boiling point ]

339.81°C (rough estimate)
[density ]

1.0441 (rough estimate)
[refractive index ]

1.6100 (estimate)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

Chloroform (Sparingly), Methanol (Slightly, Heated)
[form ]

solid
[pka]

pKa 10.3 (Uncertain)
[color ]

White to Off-White
[Water Solubility ]

Insoluble
[Merck ]

13,318
[InChI]

1S/C9H18N6/c1-13(2)7-10-8(14(3)4)12-9(11-7)15(5)6/h1-6H3
[InChIKey]

UUVWYPNAQBNQJQ-UHFFFAOYSA-N
[SMILES]

CN(C)c1nc(nc(n1)N(C)C)N(C)C
[CAS DataBase Reference]

645-05-6(CAS DataBase Reference)
[NIST Chemistry Reference]

Altretamine(645-05-6)
[EPA Substance Registry System]

645-05-6(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[RTECS ]

OS1050000
[HS Code ]

2933690000
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
[Hazardous Substances Data]

645-05-6(Hazardous Substances Data)
[Toxicity]

LD50 in rats, guinea pigs (mg/kg): 350, 255 orally (Jasper)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Dimethylamine-->Cyanuric chloride-->Hydrogen-->2,4,6-Tris[bis(methoxymethyl)amino]-1,3,5-triazine
Hazard InformationBack Directory
[General Description]

Colorless crystalline solid. Insoluble in water.
[Reactivity Profile]

HEXAMETHYLMELAMINE(645-05-6) neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
[Air & Water Reactions]

Insoluble in water.
[Hazard]

Toxic.
[Chemical Properties]

White Solid
[Originator]

Hexastat,Roger Bellon,France,1979
[Uses]

An antitumor agent which also acts as a chemosterilant for male houseflies and other insects. Antineoplastic.
[Uses]

antimalarial
[Uses]

As experimental insect chemosterilant.
[Indications]

Although both DNA and RNA synthesis are inhibited in cells exposed to hexamethylmelamine (Hexalen), the molecular mechanisms of these effects are not known.
[Production Methods]

Commercial manufacture of altretamine follows a simple, high yield alkylation sequence built around melamine as the core heterocycle. Producers first generate an excess of dimethyl sulphate or methyl chloride under controlled alkaline conditions, then carry out exhaustive N methylation of melamine’s three exocyclic amino groups to form the fully substituted hexamethylated triaminotriazine. The reaction is typically run in polar solvents with a base to neutralise the liberated acid, followed by purification through crystallisation to remove partially methylated by products.
[Manufacturing Process]

50 g of hexamethylolmelamine-hexamethyl ether in 950 cc methanol are hydrogenated, at 90°C to 100°C, in the presence of 2 g Raney nickel with 100 atmospheres excess pressure of hydrogen in a steel autoclave holding 2 L until the absorption of hydrogen is terminated. After the catalyst has been filtered off with suction, the methanol is distilled off. As a result, 23.1 g (86% of the theoretical) of crude hexamethylmelamine are formed having a melting point of 158°C to 162°C. After recrystallization from methanol, the pure product is obtained having a melting point of 168°C.
[Brand name]

Hexalen (Millot Laboratories, France).
[Therapeutic Function]

Antitumor
[Mechanism of action]

Hexamethylmelamine is readily absorbed after oral administration, with peak plasma levels achieved after 1 hour.The drug is readily metabolized to form a number of demethylated metabolites. Urinary elimination is the primary route of drug excretion.
[Clinical Use]

Hexamethylmelamine is useful for the treatment of ovarian adenocarcinoma and is frequently combined with cyclophosphamide, cisplatin, and doxorubicin in the treatment of this tumor. It also has some activity against small cell lung cancer.
[Side effects]

Nausea and vomiting are the major toxicities associated with hexamethylmelamine administration. Myelosuppression and a peripheral neuropathy also may occur.
[Metabolism]

This unique structure is believed to damage tumor cells through the production of the weakly alkylating species formaldehyde, a product of CYP450-mediated N-demethylation. Administered orally, altretamine is extensively metabolized on first pass, producing primarily mono- and didemethylated metabolites. Additional demethylation reactions occur in tumor cells, releasing formaldehyde in situ before the drug is excreted in the urine.
[Pesticide Type]

Insecticide
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

2,4,6-Tris(dimethylamino)-1,3,5-triazine(645-05-6).msds
Spectrum DetailBack Directory
[Spectrum Detail]

Altretamine(645-05-6)1HNMR
Altretamine(645-05-6)IR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

645-05-6(sigmaaldrich)
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