2,3-Dimercapto-1-propanol tributyrate

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Reagent Code: #180189
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CAS Number 58428-97-0

science Other reagents with same CAS 58428-97-0

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Weight 334.49 g/mol
Formula C₁₅H₂₆O₄S₂
badge Registry Numbers
MDL Number MFCD00010601
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an antidote for heavy metal poisoning, particularly effective in cases involving arsenic, mercury, and lead. It functions by chelating toxic metals, forming water-soluble complexes that are excreted through urine, thereby reducing metal accumulation in vital organs. Commonly administered in clinical settings following acute exposure or in chronic poisoning cases where metal detoxification is required. Its esterified form enhances lipid solubility, allowing better tissue penetration and improved bioavailability compared to non-esterified analogs. Also investigated for use in mitigating oxidative stress associated with metal toxicity due to the presence of thiol groups that can scavenge free radicals.

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inventory 1g
10-20 days ฿10,020.00

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2,3-Dimercapto-1-propanol tributyrate
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Used as an antidote for heavy metal poisoning, particularly effective in cases involving arsenic, mercury, and lead. It functions by chelating toxic metals, forming water-soluble complexes that are excreted through urine, thereby reducing metal accumulation in vital organs. Commonly administered in clinical settings following acute exposure or in chronic poisoning cases where metal detoxification is required. Its esterified form enhances lipid solubility, allowing better tissue penetration and improved bioa
Used as an antidote for heavy metal poisoning, particularly effective in cases involving arsenic, mercury, and lead. It functions by chelating toxic metals, forming water-soluble complexes that are excreted through urine, thereby reducing metal accumulation in vital organs. Commonly administered in clinical settings following acute exposure or in chronic poisoning cases where metal detoxification is required. Its esterified form enhances lipid solubility, allowing better tissue penetration and improved bioavailability compared to non-esterified analogs. Also investigated for use in mitigating oxidative stress associated with metal toxicity due to the presence of thiol groups that can scavenge free radicals.
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