Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gadolinium | HCID 23982 | — |
| Reactant | Acetic acid, gadolinium(3+) salt (3:1) | HCID 159771 | — |
| Reactant | HCID 9946216 | HCID 9946216 | — |
| Product | HCID 19838415 | HCID 19838415 | — |
Reaction Steps
Thirty mg of 4,7,10-triscarboxymethyl-1-oxa-4, 7,10-triazacyclododecane (see Example 1) was added to 0.7 ml of 100 mM gadolinium acetate. The solution was adjusted to pH 3 and heated at 88° C. for 20 minutes. A precipitate was visible when the solution was adjusted to pH 7.3. 4,7,10-Triscarboxymethyl-1-oxa-4,7,10-triazacyclododecane (16 mg) was added, the solution adjusted to pH 3 and heated at 88° C. for 20 minutes. On adjustment to pH 7.3, a slight precipitate was observed. Twenty mg of 4,7,10-triscarboxymethyl-l-oxa-4,7,10-triazacyclododecane was added and the solution was adjusted to pH 3.0. Reheating under the same conditions resulted in reducing the free gadolinium to 0.22±0.18% as measured by paper thin layer chromatography of a radiolabeled chelate solution. The final chelate solution was clear at pH 7.3. It was passed through a 0.22 μ filter (Millipore) into a vial and sealed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05846519 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-57b978d972434fc1bd5f7eeee3bae3e2 |
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| Source note | uspto-grants-1998_12 |
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