HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979752Generated: October 29, 2026
6-Benzamidohexanoic acid → HCID 53799883, compound
https://huagongshe.com/reaction/979752
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Benzamidohexanoic acid | HCID 70388 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Perboric acid, sodium salt, monohydrate | HCID 23695970 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53799883 | HCID 53799883 | — |
Reaction Steps
Perhydrolysis of the above phenolsulfonate ester to yield 6-benzoylaminoperoxycaproic acid was accomplished according to the following procedure. To 4 L of 95° F. city water was added 5.00 g (1250 ppm) of an alkaline detergent granule, 0.36 g (90 ppm) of sodium perborate monohydrate and 0.46 g (115 ppm) of the sodium salt of the phenolsulfonate ester of 6-benzoylaminocaproic acid (0.67 g of the 69% mixture described above). Perhydrolysis of the ester to form 6-benzoylamino-peroxycaproic acid was followed by analysis of the solution for available oxygen (AvO) using a conventional iodometric titration. Complete conversion of the ester to the peroxyacid would result in the formation of 4.5 ppm AvO. The results obtained for AvO versus time are tabulated below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04634551 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-ed2b13da26ca4d7fa50f79178a4f3ee9 |
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| Source note | uspto-grants-1987_01 |
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