6998-83-0

Basic information

• Product Name: TRIMETHYL CIS,CIS-1,3,5-CYCLOHEXANETRICARBOXYLATE
• Synonyms: TRIMETHYL CIS-1,3,5-CYCLOHEXANETRICARBOXYLATE;TRIMETHYL CIS,CIS-1,3,5-CYCLOHEXANETRICARBOXYLATE;Trimethylcis-1,3,5-cyclohexanetricarboxylate,98%;1,3,5-Cyclohexanetricarboxylic acid trimethyl est;(1alpha,3alpha,5alpha)-1,3,5-Cyclohexanetricarboxylic acid trimethyl ester
• CAS NO: 6998-83-0
• Molecular Formula: C₁₂H₁₈O₆
• Molecular Weight: 258.27
• Product Categories: C12 to C63;Carbonyl Compounds;Esters
• Mol File: 6998-83-0.mol
• Article Data: 5

Chemical Properties

• Melting Point: 46-49 °C(lit.)
• Boiling Point: 332.848 °C at 760 mmHg
• Flash Point: >230 °F
• Appearance: solid
• Density: 1.177±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.464
• CAS DataBase Reference: TRIMETHYL CIS,CIS-1,3,5-CYCLOHEXANETRICARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: TRIMETHYL CIS,CIS-1,3,5-CYCLOHEXANETRICARBOXYLATE(6998-83-0)
• EPA Substance Registry System: TRIMETHYL CIS,CIS-1,3,5-CYCLOHEXANETRICARBOXYLATE(6998-83-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 6998-83-0(Hazardous Substances Data)

Usage

General Description

TRIMETHYL CIS,CIS-1,3,5-CYCLOHEXANETRICARBOXYLATE, also known as trimellitic acid triester, is a chemical compound with the molecular formula C15H24O6. It is a colorless to light yellow liquid that is commonly used as a plasticizer and a component in the production of various plastics, resins, and coatings. This chemical is known for its ability to improve the flexibility, durability, and performance of these materials. It is also used in the manufacturing of adhesives, sealants, and lubricants. TRIMETHYL CIS,CIS-1,3,5-CYCLOHEXANETRICARBOXYLATE has low volatility and is considered to be stable under normal conditions, making it a versatile and valuable ingredient in the production of a wide range of industrial and consumer products.

InChI:InChI=1/C12H18O6/c1-16-10(13)7-4-8(11(14)17-2)6-9(5-7)12(15)18-3/h7-9H,4-6H2,1-3H3/t7-,8+,9-

Upstream product

• 2672-58-4 1,3,5-tris-(methoxycarbonyl)benzene 
• 67-56-1 methanol 
• 16526-68-4 cis-1,3,5-cyclohexane tricarboxylic acid 
• 554-95-0 benzene-1,3,5-tricarboxylic acid 
• 147365-19-3 (1S,3S,5S)-cyclohexane-1,3,5-tricarbonyl trichloride 

Downstream Products

• 5962-82-3 cis,cis-1,3,5-tris(hydroxymethyl)cyclohexane 
• 16526-68-4 cis-1,3,5-cyclohexane tricarboxylic acid 
• 79410-20-1 Kemp's triacid 
• 118514-35-5 cis,cis-1,3,5-trimethylcyclohexane-1,3,5-tricarboxylic acid 
• 165059-15-4 cis,cis-1,3,5-tris(diphenylphosphino)-1,3,5-tris-(methoxycarbonyl)cyclohexane 
• 253200-54-3 1,3,5-triisopropyl-cyclohexane-1,3,5-tricarboxylic acid trimethyl ester 
• 79410-21-2 trimethyl-cis,cis-1,3,5-trimethyl-1,3,5-cyclohexane-tricarboxylate 
• 107271-35-2 trimethyl cis,trans-1,3,5-trimethylcyclohexane-1,3,5-tricarboxylate 
• 117873-95-7 (1R,5S,7S)-1,5,7-Trimethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid phenylamide 
• 107354-37-0 cis,cis-1,3,5-trisformylcyclohexane 
• 107383-97-1 [1-{3,5-Bis-[(E)-methyliminomethyl]-cyclohexyl}-meth-(E)-ylidene]-methyl-amine 
• 107384-06-5 [1-{3,5-Bis-[(E)-ethyliminomethyl]-cyclohexyl}-meth-(E)-ylidene]-ethyl-amine 
• 107383-99-3 [1-(3,5-Bis-hydrazonomethyl-cyclohexyl)-meth-(E)-ylidene]-hydrazine 
• 107383-96-0 cis,cis-1,3,5-tris<(isopropylimino)methyl>cyclohexane 

Relevant articles and documents

Indoline Catalyzed Acylhydrazone/Oxime Condensation under Neutral Aqueous Conditions

Acylhydrazones formation has been widely applied in materials science and biolabeling. However, their sluggish condensation rate under neutral conditions limits its application. Herein, indolines with electron-donating groups are reported as a new catalyst scaffold, which can catalyze acylhydrazone, hydrazone, and oxime formation via an iminium ion intermediate. This new type of catalyst showed up to 15-fold rate enhancement over the traditional anilinecatalyzed reaction at neutral conditions. The identified indoline catalyst was successfully applied in hydrogel formation.

A flexible solution to anion transport: Powerful anionophores based on a cyclohexane scaffold

Transmembrane anion carriers (anionophores) have potential for biological activity, including the treatment of channelopathies such as cystic fibrosis. A new family of anionophores has been synthesized, in which three thiourea groups are mounted on a cyclohexane-based scaffold. Though conceptually related to earlier polycyclic systems, these molecules are simpler and far more accessible. Preorganization is somewhat reduced compared to earlier systems, and anion affinities are correspondingly lower. However, transport activities set new records. This surprising performance suggests a role for controlled flexibility in the design of transmembrane anion carriers. Speedy shuttling: New anionophores were developed which are simpler and far more accessible than conceptually related earlier systems. They are also less preorganized and anion affinities are lower (as expected), but transport activities set new records. This surprising performance suggests a role for controlled flexibility in the design of transmembrane anion carriers.

Synthesis of 3,5,12-Triazawurtzitanes ( 3,5,12-Triazatetracyclo2,604,9>dodecanes

The first examples of 3,5,12-triazawurtzitanes (3,5,12-triazatetracyclo2,604,9>dodecanes are described. cis, cis - 1.3.5-Triformylcyclohexane (8) has been synthesised by Swern oxidation of cis, cis - 1.3.5-tris(hydroxymethyl