Polymethacrylate Copolymer (N−C4−52−6.9)

Cat. No.: HY-160726 Purity: ≥99.0%: FAQs
Data Sheet SDS COA Handling Instructions

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Polymethacrylate Copolymer N−C4−52−6.9 is a polymer that consists of hydrophobic butylmethacrylate and cationic methacroylcholine chloride monomers. Polymethacrylate Copolymer N−C4−52−6.9 is able to solubilise lipid bilayers into nanodiscs. Polymethacrylate Copolymer N−C4−52−6.9 can be utilized in structure and functional studies on membrane proteins.

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Polymethacrylate Copolymer (N−C4−52−6.9) Chemical Structure

CAS No. : 2315261-99-3

Size	Price	Stock	Quantity
5 mg	USD 120	In-stock	Estimated Time of Arrival: December 31
10 mg	USD 200	In-stock	Estimated Time of Arrival: December 31
25 mg	USD 390	In-stock	Estimated Time of Arrival: December 31
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Other Forms of Polymethacrylate Copolymer (N−C4−52−6.9):

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Description	Polymethacrylate Copolymer N−C4−52−6.9 is a polymer that consists of hydrophobic butylmethacrylate and cationic methacroylcholine chloride monomers. Polymethacrylate Copolymer N−C4−52−6.9 is able to solubilise lipid bilayers into nanodiscs. Polymethacrylate Copolymer N−C4−52−6.9 can be utilized in structure and functional studies on membrane proteins^[1].
Formula	(C₉H₁₈NO₂.C₈H₁₄O₂.Cl)x.C₄H₈O₂S
CAS No.	2315261-99-3
Appearance	Solid
Color	Off-white to light yellow
SMILES	COC(CCSCC(C(OCC[N+](C)(C)C)=O)(C)CC(C)([H])C(OCCCC)=O)=O.[Cl-].[0.52].[0.48].[n]
Shipping	Room temperature in continental US; may vary elsewhere.
Storage	-20°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Solvent & Solubility	In Vitro: DMSO : 10 mg/mL (Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) Molarity Calculator Dilution Calculator Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol) Mass = Concentration × Volume × Molecular Weight * Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final) This equation is commonly abbreviated as: C₁V₁ = C₂V₂ Concentration _(start) C1 × Volume _(start) V1 = Concentration _(final) C2 × Volume _(final) V2 In Vivo Dissolution Calculator Please enter the basic information of animal experiments: Dosage mg/kg Animal weight (per animal) g Dosing volume (per animal) μL Number of animals Recommended: Prepare an additional quantity of animals to account for potential losses during experiments. Calculation results: Working solution concentration: mg/mL
Purity & Documentation	Purity: ≥99.0% Select Batch: Data Sheet (270 KB) SDS (252 KB) COA (251 KB) Handling Instructions (2659 KB)
References	[1]. Lavington S, et al., Detergent-free solubilisation & purification of a G protein coupled receptor using a polymethacrylate polymer. Biochim Biophys Acta Biomembr. 2021 Jan 1;1863(1):183441. [Content Brief]