Bisphenol A bis(3-chloro-2-hydroxypropyl) ether-d₁₄

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Bisphenol A bis(3-chloro-2-hydroxypropyl) ether-d₁₄ is deuterium labeled Bisphenol A bis(3-chloro-2-hydroxypropyl) ether. Bisphenol A bis(3-chloro-2-hydroxypropyl) ether is an organic compound with potential antimicrobial activity. Bisphenol A bis(3-chloro-2-hydroxypropyl) ether can be widely used in coatings and plastics to improve the strength and durability of materials. Bisphenol A bis(3-chloro-2-hydroxypropyl) ether also plays an important role in textile processing, improving the wrinkle resistance and abrasion resistance of fabrics.

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Bisphenol A bis(3-chloro-2-hydroxypropyl) ether-d<sub>14</sub> Chemical Structure

Bisphenol A bis(3-chloro-2-hydroxypropyl) ether-d₁₄ Chemical Structure

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Other Forms of Bisphenol A bis(3-chloro-2-hydroxypropyl) ether-d₁₄:

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Description	Bisphenol A bis(3-chloro-2-hydroxypropyl) ether-d₁₄ is deuterium labeled Bisphenol A bis(3-chloro-2-hydroxypropyl) ether. Bisphenol A bis(3-chloro-2-hydroxypropyl) ether is an organic compound with potential antimicrobial activity. Bisphenol A bis(3-chloro-2-hydroxypropyl) ether can be widely used in coatings and plastics to improve the strength and durability of materials. Bisphenol A bis(3-chloro-2-hydroxypropyl) ether also plays an important role in textile processing, improving the wrinkle resistance and abrasion resistance of fabrics^[1].
Molecular Weight	427.42
Formula	C₂₁H₁₂D₁₄Cl₂O₄
Unlabeled CAS	4809-35-2
SMILES	ClCC(COC1=C([2H])C([2H])=C(C(C([2H])([2H])[2H])(C([2H])([2H])[2H])C2=C([2H])C([2H])=C(C([2H])=C2[2H])OCC(CCl)O)C([2H])=C1[2H])O
Shipping	Room temperature in continental US; may vary elsewhere.
Storage	Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation	Data Sheet (268 KB) Handling Instructions (2659 KB)
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief] [2]. Inhibition of c-Src protects paraquat induced microvascular endothelial injury by modulating caveolin-1 phosphorylation and caveolae mediated transcellular permeabilityYu H and Qing HEnvironmental Toxicology and Pharmacology2017 [3]. Field Dissiation Kinetics of Paraquat in Acid Soil as Function of Concentration and its Residues in Tea LeavesJanaki