Diethylenetriaminepentaacetic acid → DTPA dianhydride

HRID 2392506Notes

Reaction equation

HRID 2392506 reaction equation
[CH2:1]([N:12]([CH2:24][C:25]([OH:27])=[O:26])[CH2:13][CH2:14][N:15]([CH2:20][C:21]([OH:23])=O)[CH2:16][C:17]([OH:19])=[O:18])[CH2:2][N:3]([CH2:8][C:9]([OH:11])=[O:10])[CH2:4][C:5]([OH:7])=O>C(Cl)(Cl)Cl>[CH2:20]1[N:15]([CH2:14][CH2:13][N:12]([CH2:24][C:25]([OH:27])=[O:26])[CH2:1][CH2:2][N:3]2[CH2:8][C:9](=[O:10])[O:11][C:5](=[O:7])[CH2:4]2)[CH2:16][C:17](=[O:19])[O:18][C:21]1=[O:23]

Participants

3

Reactant 1

HCID 3053Diethylenetriaminepentaacetic acid

Product 1

HCID 100825DTPA dianhydride

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Procedure

A 0.1 mg/ml solution of DTPA anhydride in dry chloroform was prepared and an aliquot containing the desired quantity of DTPA was added to a reaction vessel. The chloroform was removed by evaporation with nitrogen gas at room temperature. A pH 7.0 solution of antibody (approximately 0.5 mg) in 0.05M bicarbonate buffer was added to said reaction vessel to produce a 7:1 molar ratio of anhydride to protein. The solution was incubated with shaking for one minute and the coupled antibody was recovered by passage over a Sephadex G-50 column.

Workup

  1. additionwas added to a reaction vessel
  2. customThe chloroform was removed by evaporation with nitrogen gas at room temperature
  3. additionA pH 7.0 solution of antibody (approximately 0.5 mg) in 0.05M bicarbonate buffer was added
  4. customreaction vessel
  5. customto produce a 7
  6. customthe coupled antibody was recovered by passage over a Sephadex G-50 column

Sources & evidence

ORD record
ord-be69e6d557b847bf9ba8f9079ead547d
Source dataset
uspto-grants-1998_09
Patent number
US05800802

Reaction notes

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