- Progoitrin
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- $562.00
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2026-07-16
- CAS:585-95-5
- Purity: 98.75%
- Supply Ability: 10g
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| | Progoitrin Basic information |
| Product Name: | Progoitrin | | Synonyms: | 1-[(R)-1-[(Sulfooxy)imino]-3-hydroxy-4-pentenyl]-1-thio-β-D-glucopyranose;Glucorapiferin;(R)-2-Hydroxy-3-butenyl glucosinolate;2(R)-Hydroxy-3-butenyl glucosinolate;beta-D-Glucopyranose, 1-thio-, 1-((3R)-3-hydroxy-N-(sulfooxy)-4-pentenimidate;beta-D-Glucopyranose, 1-thio-, 1-(3-hydroxy-N-(sulfooxy)-4-pentenimidate), (R)-;Glucopyranose, 1-thio-, 1-((R)-3-hydroxy-4-pentenohydroximate) no-(hydrogen sulfate), beta-D-;progoitrin(1-) | | CAS: | 585-95-5 | | MF: | C11H19NO10S2 | | MW: | 389.4 | | EINECS: | | | Product Categories: | | | Mol File: | 585-95-5.mol |  |
| | Progoitrin Chemical Properties |
| density | 1.79±0.1 g/cm3(Predicted) | | Melting point | 178-181 °C | | pKa | -3.13±0.18(Predicted) | | form | Solid | | color | White to off-white |
| | Progoitrin Usage And Synthesis |
| Uses | Progoitrin is the dominant glucosinolate in incriminated crops. Antithyroid activity[1][2]. | | Definition | ChEBI: The stereoisomer of xi-progoitrin that has R at the carbon bearing the allylic hydroxy group. | | References | [1] Collett MG, et al. Hepatotoxicity of Two Progoitrin-Derived Nitriles in New Zealand White Rabbits. Toxins (Basel). 2020;12(11):695. Published 2020 Nov 2. DOI:10.3390/toxins12110695
[2] GREER MA, et al. Antithyroid activity elicited by the ingestion of pure progoitrin, a naturally occurring thioglycoside of the turnip family. J Clin Invest. 1959;38(9):1465-1474. DOI:10.1172/JCI103923 |
| | Progoitrin Preparation Products And Raw materials |
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