peracetic acid suppliers USA

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Peracetic Acid Peracetic Acid. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. Redox
North America & APAC
3,4-Epoxycyclohexylmethyl 3,4-Epoxycyclohexanecarboxylate 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate (EEC) is a cycloaliphatic epoxy that can be synthesized by the reaction of 3'-cyclohexenylmethyl 3-cyclohexenecarboxylate with peracetic acid. Its aliphatic backbone and molecular structure provide a number of useful properties such as thermal stability, weatherability, and electrical conductivity. Uses: Eec is an epoxy monomer that can be used as a resin in aerospace, electronics and automobile industries as an adhesive and a composite material. Group: Monomers. Alternative Names: 7-Oxabicyclo[4.1.0]Heptan-3-Ylmethyl 7-Oxabicyclo[4.1.0]Heptane-3-Carboxylate. CAS No. 2386-87-0. Pack Sizes: Packaging 50, 250 mL in poly bottle. Product ID: 7-oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate. Molecular formula: 252.31. Mole weight: C14H20O4. C1CC2C(O2)CC1COC(=O)C3CCC4C(C3)O4. InChI=1S/C14H20O4/c15-14 (9-2-4-11-13 (6-9)18-11)16-7-8-1-3-10-12 (5-8)17-10/h8-13H, 1-7H2. YXALYBMHAYZKAP-UHFFFAOYSA-N. 95%+. Alfa Chemistry Materials 6
2,4,7,8,9-Penta-O-acetyl-N-azidoacetyl-b-neuraminic acid methyl ester 2,4,7,8,9-Penta-O-acetyl-N-azidoacetyl-b-neuraminic acid methyl ester, an indispensable biomedical compound, demonstrates exceptional proficiency in synthesizing and refining antiviral pharmaceuticals. Its paramount significance manifests in effectively combating an array of virus-induced infections, namely influenza and herpes. Synonyms: Peracetyl-N-(2-azidoacetyl)-b-neuraminic acid methyl ester; Ac5NeuNAz-O-Me. CAS No. 1357804-21-7. Molecular formula: C22H30N4O14. Mole weight: 574.49. BOC Sciences 3
2-Acetamido-3,4-di-O-acetyl-6-O-[a-2-(4,7,8,9-tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester)]-2-deoxy-a-D-galactopyranosyl Fmocthreonine 2-Acetamido-3,4-di-O-acetyl-6-O-[a-2-(4,7,8,9-tetra-O-acetyl-N-acetyl-D-neuraminic acid methyl ester)]-2-deoxy-a-D-galactopyranosyl Fmocthreonine exhibits efficacy in combatting viral and bacterial afflictions. Synonyms: STn Antigen (Threonine, Fmoc, peracetylated, methyl ester). Molecular formula: C51H63N3O24. Mole weight: 1102.05. BOC Sciences 4
3FAx-Neu5Ac 3FAx-Neu5Ac (Compound 8), a Sialic acid peracetylated analog, is a sialyltransferase inhibitor. 3FAx-Neu5Ac substantially reduces expression of the sialylated ligand sialyl Lewis X[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 117405-58-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110288. MedChemExpress MCE
5-[(3,4,6-Tri-O-acetyl-2-acetylamido-2-deoxy-b-D-galactopyranosyl)oxy]pentanoic acid A linker that incorporates TLR4 inhibitor TLR4-IN-C34. It is also a molecular building block belonging to the GalNAc series or related delivery systems. Synonyms: TLR4-IN-C34-C2-COOH; Peracetylated GalNAc Pentenoic Acid; 5-[[3,4,6-Tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]pentanoic acid; 5-(((2R,3R,4R,5R,6R)-3-Acetamido-4,5-diacetoxy-6-(acetoxymethyl)tetrahydro-2H-pyran-2-yl)oxy)pentanoic acid; 5-([(2R,3R,4R,5R,6R)-4,5-Bis(acetyloxy)-6-[(acetyloxy)methyl]-3-acetamidooxan-2-yl]oxy)pentanoic acid. Grade: ≥95%. CAS No. 1159408-54-4. Molecular formula: C19H29NO11. Mole weight: 447.43. BOC Sciences 5
Peracetylated GalNAc-L96-Acid-1 It is a molecular building block belonging to the GalNAc series or related delivery systems. It is also a complex organic compound used in the synthesis of peptides and proteins. This compound is commonly used as a coupling agent to activate carboxylic groups on amino acids, thereby aiding in the formation of peptide bonds. Synonyms: 3-[2-Benzyloxycarbonylamino-3-(2-carboxy-ethoxy)-2-(2-carboxy-ethoxymethyl)-propoxy]-propionic acid; 3,3'-[[2-[(2-Carboxyethoxy)methyl]-2-[[(phenylmethoxy)carbonyl]amino]-1,3-propanediyl]bis(oxy)]bis[propanoic acid]; Cbz-N-tris tri-acid; Cbz-N-amido-tri-(carboxyethoxymethyl)-methane. Grade: ≥95%. CAS No. 200133-16-0. Molecular formula: C21H29NO11. Mole weight: 471.46. BOC Sciences

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