HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702154Generated: October 25, 2026
Hydrochloric Acid → Nicotinamide adenine dinucleotide biotin
https://huagongshe.com/reaction/1702154
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-Cyclohexyl-3-(2-morpholinoethyl)carbodiimide | HCID 84998 | — |
| Reactant | Biotin | HCID 171548 | — |
| Reactant | Nicotinamide-6(2-aminoethylamino)purine dinucleotide | HCID 191523 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | Nicotinamide adenine dinucleotide biotin | HCID 131711938 | — |
Reaction Steps
A 16 mg quantity of biotin was suspended in 1 ml of water containing 22 mg of nicotinamide 6-(2-aminoethylamino) purine dinucleotide prepared as in Example 1. A few drops of 0.1 N sodium hydroxide was added to aid dissolution of the biotin. A 240 mg quantity of 1-cyclohexyl-3-(2-morpholinoethyl)-carbodiimide metho-p-toluene sulfonate was added to the resulting solution and brought into solution by dropwise addition of 0.1 N hydrochloric acid. The reaction mixture was allowed to incubate at room temperature for 5 hours and was then poured into 10 ml of acetone at -10° C. The oil which formed was separated, washed twice with from 5 to 10 ml of ether and dissolved in from 1 to 2 ml of water. The resulting material was purified by electrophoresis on paper as in Example 1. Two fluorescent bands appeared after spraying with sodium cyanide, one having migrated toward the cathode and the other toward the anode. The latter band, which contained the NAD-biotin conjugate, was eluted with water and stored at -20° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04380580 |
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| Source dataset | uspto-grants-1983_04 |
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| ORD ID | ord-544ec99d90d5438bb0cb182791f45596 |
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| Source note | uspto-grants-1983_04 |
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