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trisethyleneiminoquinone

CAS No.
68-76-8
Chemical Name:
trisethyleneiminoquinone
Synonyms
TEIB;A 163;Trenimon;prenimon;riker 601;oncovedex;TRENIMONE;NSC-29215;bayer 3231;10257 R.P.
CBNumber:
CB6875606
Molecular Formula:
C12H13N3O2
Molecular Weight:
231.25052
MDL Number:
MFCD00866557
MOL File:
68-76-8.mol
MSDS File:
SDS
Last updated:2022-12-21 16:56:50

trisethyleneiminoquinone Properties

Melting point 162.5-163°
Boiling point 373.33°C (rough estimate)
Density 1.1818 (rough estimate)
refractive index 1.5290 (estimate)
FDA UNII F3D5D9P25I
IARC 3 (Vol. 9, Sup 7) 1987
ATC code L01AC02
EPA Substance Registry System Triaziquone (68-76-8)

SAFETY

Risk and Safety Statements

RIDADR  3249
HazardClass  6.1(a)
PackingGroup  II
Toxicity An antineoplastic agent related to thiotepa. It has considerable acute toxicity and is a probable carcinogen.

trisethyleneiminoquinone Chemical Properties,Uses,Production

Originator

Trenimon,Bayer

Uses

Alkylating reagent in mutation research.

Definition

ChEBI: A member of the class of 1,4-benzoquinones that is 1,4-benzoquinone in which three of the ring hydrogens are replaced by aziridin-1-yl groups.

Manufacturing Process

Under anaerobic conditions including an atmosphere of nitrogen, 104 ml (2.0 moles) of aziridine is added as a single portion with stirring to a suspension of 33.6 g (0.2 mole) of 2,6-dimethoxy-1,4-benzoquinone in 500 ml of absolute methanol at a temperature of 0° to 5°C. After the addition has been 2,6- dimethoxy-1,4-benzoquinone completed the external cooling of the reaction vessel is replaced by a room temperature water bath and the mixture is stirred at room temperature for 45 hours while a slow stream of nitrogen is passed therethrough to preserve the anaerobic reaction conditions. It is found that the yellow starting material, during this period, completely disappears into solution and that a violet or purple substance together with a colorless substance are formed as precipitated reaction products. This mixture of precipitated products is removed by filtration at -20°C and the residue is washed with a small quantity of cooled methanol. Then the mixture is dried in a vacuum desiccator yielding about 30.4 g of mixed product. The mixed product is extracted with benzene whereby the violet or purple colored component passes into solution and the substantially colorless product remains in a yield of about 16.0 g. The colorless 2,6-bis-aziridino-l,4- benzohydroquinone so obtained melts with decomposition at about 221-222°C with melting starting at about 200°C. It can be purified by recrystallization from a of dioxane yielding snow-white crystals that decompose when heated at 222-224°C while starting to melt at 220°C. The benzene extract of the colored reaction product is evaporated to dryness under vacuum, yielding a residue melting at 161-162°C which is recrystallized from 200 ml of ethyl acetate, filtered under suction at -20°C, washed with cold methanol and thus yields about 11.5 g of a pure, purple-colored crystalline 2,3,5-tris-aziridino-1,4-benzoquinone melting at 162.5-163°C.

Therapeutic Function

Antineoplastic

General Description

Purple needle-like crystals.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

trisethyleneiminoquinone is an amine. 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

Flash point data is not available for trisethyleneiminoquinone, but trisethyleneiminoquinone is probably combustible.

Safety Profile

Poison by intraperitoneal, intravenous, and parenteral routes. Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental carcinogenic data. Human mutation data reported. When heated to decomposition it emits toxic fumes of NOx. Used as a drug for the treatment of neoplastic dseases.

trisethyleneiminoquinone Preparation Products And Raw materials

Global( 14)Suppliers
Supplier Tel Email Country ProdList Advantage
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9340 55
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
Career Henan Chemica Co
+86-0371-86658258 15093356674; laboratory@coreychem.com China 30255 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 27644 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 9020 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 14059 65
Chizhou Kailong Import and Export Trade Co., Ltd. xg01_gj@163.com China 9503 50
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 15229059051 1027@dideu.com China 9947 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24017 58

View Lastest Price from trisethyleneiminoquinone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
trisethyleneiminoquinone USP/EP/BP pictures 2021-07-06 trisethyleneiminoquinone USP/EP/BP
68-76-8
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
trisethyleneiminoquinone pictures 2021-01-06 trisethyleneiminoquinone
68-76-8
US $1.80 / KG 1g 96%-99% 1kg/10kg/100kg Career Henan Chemica Co
10257 R.P. 2,3,5-triethyleneimino-1,4-benzoquinone 2,3,5-tris(1-aziridinyl)-2,5-cyclohexadiene-1,4-dione 2,3,5-tris(1-aziridinyl)-p-benzoquinone 2,3,5-tris(aziridinyl)-1,4-benzoquinone bayer 3231 oncovedex prenimon riker 601 TEIB Trenimon triaziquinone Triaziquone triethyleneiminobenzoquinone Tris (1-aziridinyl)-para-benzoquinone tris(1-aziridinyl)p-benzoquinone Tris(aziridinyl)-para-benzoquinone tris(trenimom) trisethyleneiminoquinone 2,3,5-TRIS(1-AZIRIDINYL)-PARA-BENZOQUINONE TRENIMONE NSC-29215 Tris(trenimon) TRIS(AZIRIDINYL)-P-BENZOQUINONE(TRIAZIQUINONE) 2,3,5-triethylenimino-p-benzoquinone 2,3,5-tris(aziridin-1-yl)cyclohexa-2,5-diene-1,4-dione 2,5-Cyclohexadiene-1,4-dione,2,3,5-tri-1-aziridinyl- 1,1',1''-(3,6-dioxo-1,4-cyclohexadiene-1,2,4-triyl)tris aziridine 2,5-Cyclohexadiene-1,4-dione, 2,3,5-tris(1-aziridinyl)- trisethyleneiminoquinone USP/EP/BP A 163 68-76-8