162709-84-4

Basic information

• Product Name: 3,4,5-Tridodecyloxy benzyl chloride
• Synonyms: 3,4,5-Tridodecyloxy benzyl chloride;3,4,5-Tris(dodecyloxy)benzyl chloride;(3,4,5)12G1-CH2Cl
• CAS NO: 162709-84-4
• Molecular Formula: C₄₃H₇₉ClO₃
• Molecular Weight: 679.53856
• Mol File: 162709-84-4.mol
• Article Data: 34

Chemical Properties

• Melting Point: 49-52 °C
• Boiling Point: 700.4±55.0 °C(Predicted)
• Appearance: /
• Density: 0.925±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 3,4,5-Tridodecyloxy benzyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,5-Tridodecyloxy benzyl chloride(162709-84-4)
• EPA Substance Registry System: 3,4,5-Tridodecyloxy benzyl chloride(162709-84-4)

Safety Data

• Hazardous Substances Data: 162709-84-4(Hazardous Substances Data)

Usage

General Description

3,4,5-Tridodecyloxy benzyl chloride is a chemical compound with the molecular formula C33H61ClO and a molecular weight of 529.34 g/mol. It is a derivative of benzyl chloride and is composed of a benzene ring with three dodecyloxy (C12H25O) substituents attached to the 3, 4, and 5 positions. This chemical is used in various industrial processes such as the synthesis of surfactants, detergents, and as a building block for the production of other organic compounds. Additionally, it can be utilized as a reagent in organic synthesis for various functional group transformations. This chemical is considered to be an irritant and harmful if swallowed, inhaled, or comes into contact with the skin, so it should be handled with caution in a controlled laboratory environment.

Upstream product

• 138433-00-8 3,4,5-tris(dodecyloxy)benzyl alcohol 
• 99-24-1 methyl galloate 
• 143-15-7 1-dodecylbromide 
• 123126-39-6 methyl [3,4,5-tris(n-dodecan-1-yloxy)]benzoate 
• 831-61-8 Ethyl gallate 
• 117241-30-2 ethyl 3,4,5-tri(dodecyloxy)benzoate 
• 112-29-8 1-bromo dodecane 
• 1228276-91-2 propyl 3,4,5-tris(n-dodecan-1-yloxy)benzoate 
• 121-79-9 Propyl gallate 
• 117241-31-3 3,4,5-tridodecyloxy benzoic acid 
• 149-91-7 3,4,5-trihydroxybenzoic acid 

Downstream Products

• 186031-55-0 methyl 3,4,5-tris[3',4',5'-tris(n-dodecan-1-yloxy)benzyloxy]benzoate 
• 902451-81-4 1-{4-[(3-phthalimidopropyl)oxy]phenylazo}-4-[3,4,5-tris(dodecan-1-yloxy)benzyloxy]benzene 
• 212627-80-0 methyl 3,5-bis[3',4',5'-tris(n-dodecan-1-yloxy)benzyloxy]benzoate 
• 886751-78-6 tris[4-(3,4,5-tridodecyloxybenzyloxy)phenyl]phosphine oxide 
• 916815-63-9 C₅₁H₉₀N₂O₃ 
• 916815-70-8 C₅₅H₈₈N₄O₅ 
• 1007402-37-0 C₈₉H₁₆₁N₂O₆⁽¹⁺⁾*Cl^(1-) 
• 1007402-39-2 C₄₆H₈₂N₂O₃ 
• 1063745-73-2 tris[4-(3,4,5-tridodecyloxybenzyloxy)phenyl]phenylmethane 
• 1063745-74-3 tris[4-(3,4,5-tridodecyloxybenzyloxy)phenyl]-4-pyridylmethane 
• 1063745-71-0 tris[4-(3,4,5-tridodecyloxybenzyloxy)phenyl]ethane 
• 1063745-70-9 tris[4-(3,4,5-tridodecyloxybenzyloxy)phenyl]methane 
• 1063743-09-8 C₁₅₀H₂₄₉N₃O₁₂ 
• 1063743-07-6 C₁₅₃H₂₅₂O₁₂ 

Relevant articles and documents

Constitutional Dynamic Selection at Low Reynolds Number in a Triple Dynamic System: Covalent Dynamic Adaptation Driven by Double Supramolecular Self-Assembly

A triple dynamic complex system has been designed, implementing a dynamic covalent process coupled to two supramolecular self-assembly steps. To this end, two dynamic covalent libraries (DCLs), DCL-1 and DCL-2, have been established on the basis of dynamic covalent C-C/C-N organo-metathesis between two Knoevenagel derivatives and two imines. Each DCL contains a barbituric acid-based Knoevenagel constituent that may undergo a sequential double self-organization process involving first the formation of hydrogen-bonded hexameric supramolecular macrocycles that subsequently undergo stacking to generate a supramolecular polymer SP yielding a viscous gel state. Both DCLs display selective self-organization-driven amplification of the constituent that leads to the SP. Dissociation of the SP on heating causes reversible randomization of the constituent distributions of the DCLs as a function of temperature. Furthermore, diverse distribution patterns of DCL-2 were induced by modulation of temperature and solvent composition. The present dynamic systems display remarkable self-organization-driven constitutional adaption and tunable composition by coupling between dynamic covalent component selection and two-stage supramolecular organization. In more general terms, they reveal dynamic adaptation by component selection in low Reynolds number conditions of living systems where frictional effects dominate inertial behavior.

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