| | 145-73-3 Basic information More.. |
| Product Name: | ENDOTHAL | | Synonyms: | 1,2-Benzenedicarboxylic acid, hexahydro-3,6-endo-oxy-;1,2-Cyclohexanedicarboxylic acid, 3,6-endo-epoxy-;3,6-endo-epoxy-2-cyclohexanedicarboxylicacid;3,6-endo-Oxohexahydrophthalic acid;3,6-endooxohexahydrophthalicacid;3,6-endo-Oxyphthalic acid hexahydro-;3,6-Endoxohexahydrophthalic acid;hexahydro-3,6-endo-oxy-2-benzenedicarboxylicacid | | CAS: | 145-73-3 | | MF: | C8H10O5 | | MW: | 186.16 | | EINECS: | 205-660-5 | | Mol File: | 145-73-3.mol |  |
Use
Biological. Incubation of 14C-ring labeled endothall (10 mg/mL) by Arthrobacter sp.,
which was isolated from pond water and a hydrosol, in aerobic sediment-water suspensions
revealed that after 30 days, 40% evolved as 14CO2. Glutamic acid was the major transformation
product. Minor products were alanine, citric and aspartic acids and unidentified
products, some of which were tentatively identified as phosphate esters (Sikka and Saxena,
1973). In pond water treated with endothall (2 and 4 ppm), detectable levels were found
after 7 days (Sikka and Rice, 1973). Biodegradation was rapid in an Ontario soil sample.
After 1 week, 70% of endothall added was converted to carbon dioxide (Simsiman et al.,
1976).
Chemical/Physical. Reacts with bases forming water-soluble salts. Above 90°C, endothall
is slowly converted to the anhydride (Windholz et al., 1983; Hartley and Kidd, 1987)
and water (Humburg et al., 1989). Endothall is stable to light (Hartley and Kidd, 1987).
- Endothall
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- US $38.00-96.00 / mg
- 2025-05-09
- CAS:145-73-3
- Min. Order:
- Purity: 98.92%
- Supply Ability: 10g
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145-73-3
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