16958-92-2

Basic information

• Product Name: DI(TRIDECYL) ADIPATE
• Synonyms: Hexanedioicacid,ditridecylester;DI(TRIDECYL) ADIPATE;bis(tridecyl) adipate;Ditridecyl hexanedioate;DTDA;Ditridecyladipat;Dilinoleic acid, ditridecyl ester;Dimer acid, ditridecyl ester
• CAS NO: 16958-92-2
• Molecular Formula: C₃₂H₆₂O₄
• Molecular Weight: 510.83
• EINECS: 241-029-0
• Mol File: 16958-92-2.mol
• Article Data: 1

Chemical Properties

• Melting Point: 45.9 °C
• Boiling Point: 503 °C at 760 mmHg
• Flash Point: 226.2 °C
• Appearance: /
• Density: 0.906 g/cm³
• Vapor Pressure: 3.03E-10mmHg at 25°C
• Refractive Index: 1.458
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), Methanol (Slightly, Heated)
• CAS DataBase Reference: DI(TRIDECYL) ADIPATE(CAS DataBase Reference)
• NIST Chemistry Reference: DI(TRIDECYL) ADIPATE(16958-92-2)
• EPA Substance Registry System: DI(TRIDECYL) ADIPATE(16958-92-2)

Safety Data

• Hazardous Substances Data: 16958-92-2(Hazardous Substances Data)

Usage

Uses

Ditridecyl Adipate can be used as a skin conditioning or fragrance ingredient, plasticizer, solvent or emollient in cosmetics. Also used in combination with other compounds as a finisher for texturing of polyester yarns.

Flammability and Explosibility

Nonflammable

InChI:InChI=1/C32H62O4/c1-3-5-7-9-11-13-15-17-19-21-25-29-35-31(33)27-23-24-28-32(34)36-30-26-22-20-18-16-14-12-10-8-6-4-2/h3-30H2,1-2H3

Upstream product

• 124-04-9 Adipic acid 
• 112-70-9 tridecan-1-ol 

Relevant articles and documents

Non-symmetric, partially fluorinated lubricant additives

Novel non-symmetric, partially fluorinated compositions and method of manufacture which are useful as lubricants or as additives to lubricant formulations involving the molecular structure: R1f—F′—R2—F″—R3h where R1frepresents a wholly or partially fluorinated organic residue end group, F′ and F″ represent functional linkages which may be alike or different, R2represents the backbone and R3hrepresents a non-fluorinated organic residue end group. Such compositions are produced by reacting a mixture of alcohols, mercaptans or amines containing at least one partially fluorinated compound and at least one non-fluorinated compound in the mixture, thus producing the R1fand the R3hresidues, with a difunctional organic compound (e.g., diacid, dinitrile, disulfonyl halide, diisocyanate, diisothiocyanate, diphosphoryl halide or dithiophosphoryl halide).