Triethylene glycol diglycidyl ether
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Triethylene glycol diglycidyl ether
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CAS No:
1954-28-5
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Formula:
C12H22O6
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Chemical Name:
Triethylene glycol diglycidyl ether
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Synonyms:
Oxirane,2,2′-(2,5,8,11-tetraoxadodecane-1,12-diyl)bis-;4,7,10,13-Tetraoxahexadecane,1,2:15,16-diepoxy-;2,2′-(2,5,8,11-Tetraoxadodecane-1,12-diyl)bis[oxirane];1,2:15,16-Diepoxy-4,7,10,13-tetraoxahexadecane;Epodyl;Etoglucid;Triethylene glycol diglycidyl ether;Ethane,1,2-bis[2-(2,3-epoxypropoxy)ethoxy]-;2,2′-(2,5,8,11-Tetraoxa-1,12-dodecanediyl)bisoxirane;1,2-Bis[2-(2,3-epoxypropoxy)ethoxy]ethane;ICI 32865;Ethoglucid;TDE;Etoglucide;Diglycidyltriethylene glycol;Ayerst 62013;NSC 80439;2-[2-[2-[2-(Oxiran-2-ylmethoxy)ethoxy]ethoxy]ethoxymethyl]oxirane;156366-23-3;2102862-83-7
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CAS No:
Description
COLOURLESS LIQUID.
Triethylene glycol diglycidyl ether is an epoxide.|Etoglucid is an epoxide compound with potential antineoplastic alkylating activity. Etoglucid is able to crosslink DNA via its epoxide group, resulting in disruption of DNA function and cell cycle arrest.|Alkylating antineoplastic agent used especially in bladder neoplasms. It is toxic to hair follicles, gastro-intestinal tract, and vasculature.
Triethylene glycol diglycidyl ether Basic Attributes
262.30 g/mol
262.30
217-784-7
4F9KUA0T4D
0204
80439
C489
L - Antineoplastic and immunomodulating agents
Characteristics
62 Ų
1.13 g/cm3
-15--11 °C
195-197 °C @ Press: 2.0 Torr
Relative vapor density (air = 1): 9.0
Safety Information
XF0700000
Combustible.
Use water spray, powder, foam, carbon dioxide.
Collect leaking and spilled liquid in sealable containers as far as possible. Wash away remainder with plenty of water.
Separated from strong oxidants.
No indication can be given about the rate at which a harmful concentration of this substance in the air is reached on evaporation at 20 °C.
NO open flames.
Use ventilation.
Protective gloves.
Wear safety spectacles.
Drug Information
A class of drugs that differs from other alkylating agents used clinically in that they are monofunctional and thus unable to cross-link cellular macromolecules. Among their common properties are a requirement for metabolic activation to intermediates with antitumor efficacy and the presence in their chemical structures of N-methyl groups, that after metabolism, can covalently modify cellular DNA. The precise mechanisms by which each of these drugs acts to kill tumor cells are not completely understood. (From AMA, Drug Evaluations Annual, 1994, p2026) (See all compounds classified as Antineoplastic Agents, Alkylating.)
Fresh air, rest.
Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Epodyl
The substance can be absorbed into the body by inhalation.
Computed Properties
Molecular Weight:262.30
XLogP3:-1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:13
Exact Mass:262.14163842
Monoisotopic Mass:262.14163842
Topological Polar Surface Area:62
Heavy Atom Count:18
Complexity:191
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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