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Detail of "16958-92-2"

  • MSDS Download
  • CAS Number:
  • 16958-92-2
  • Name:
  • Hexanedioic acid,1,6-ditridecyl ester

  • Molecular Structure:
  • Formula:
  • C32H62O4
  • Molecular Weight:
  • 510.8323
  • Synonyms:
  • Adipicacid, ditridecyl ester (7CI,8CI);Hexanedioic acid, ditridecyl ester (9CI);1-Tridecanol, adipate (2:1) (8CI);Bis(tridecyl) adipate;Ditridecyl adipate;Emkarate DTDA;Esterex A 51;Plasthall DTDA;
  • EINECS:
  • 241-029-0
  • Density:
  • 0.906 g/cm3
  • Boiling Point:
  • 503 °C at 760 mmHg
  • Flash Point:
  • 226.2 °C

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CAS No.16958-92-2 Hexanedioic acid,1,6-ditridecyl ester

Ditridecyl adipate CAS 16958-92-2 Uses: Plasticizer

Supplier:Velsicol Chemical Corp [ United States]

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Tel:847-298-9000; 800-843-7759

Address:10400 W. Higgins Road, Suite 600, Rosemont, IL, 60018, USA

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CAS No.16958-92-2 Hexanedioic acid,1,6-ditridecyl ester

more information,pls contact with us!

Supplier:Scientific Polymer Products, Inc [ United States]

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Tel:585 265 0413

Address:6265 Dean Parkway Ontario, New York 14519 U.S.A.

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CAS No.16958-92-2 Hexanedioic acid,1,6-ditridecyl ester

Supplier:Krahn Chemie GmbH [ Germany]

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Tel:+49-(40)-320 92-0

Address:Grimm 10 20457 Hamburg

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CAS No.16958-92-2 Hexanedioic acid,1,6-ditridecyl ester

Supplier:Adikem Sdn Bhd [ Malaysia]

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Tel:+6037364615

Address:Lot 2 & 4, Jalan PJS 11/5, Bandar Sunway, 46150 Petaling Jaya, Selangor Darul Ehsan, Malaysia

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CAS No.16958-92-2 Hexanedioic acid,1,6-ditridecyl ester

Supplier:Parabor Colombia [ Colombia]

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Tel:+57-1-600-7777

Address:Calle 21 # 43A-14, Bogotá, D.C. Colombia

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Reference

Antiwear additive mixture
Antiwear additive mixture. Pratt, Robert E.; Habzansky, John (Bray Oil Co., USA). U.S. US 3970570 20 Jul 1976, 4 pp. (English). (United States of America). CODEN: USXXAM. CLASS: IC: C10M001-10. NCL: 252049900. APPLICATION: US 75-638468 8 Dec 1975. DOCUMENT TYPE: Patent CA Section: 51 (Fossil Fuels, Derivatives, and Related Products) The antiwear properties of lubricating oils are improved by the addn. of a mixt. of 1-2 wt. % tricresyl phosphate (I) [1330-78-5] and 0.5-1 wt. % pentaerythritol monooleate (II) [10332-32-8]. This synergistic additive combination is ashless, has good oxidn. stability, and is noncorrosive to Cu at >300.degree.F. Thus, a prototype gas turbine lubricating oil (viscosity .apprx.6 cSt at 210.degree.F, flash point >450.degree.F, pour point <-65.degree.F) was prepd. using as base oil a hydrogenated linear .alpha.-olefin oligomer produced by the polymn. of 1-decene. An antioxidant, a seal-swell agent, and a metal deactivator were added, along with varying amts. of I and II. The antiwear properties of the blends were tested in the Falex lubricant tester and in the Shell 4-ball app. The blends contg. 10332-32-8 and 71-43-2 are just another two chemicals used in this study. I and II had better antiwear properties than the blends contg. I or II only. The additive combination was also effective when the base oil used was ridecyl adipate [16958-92-2], C10-15 dialkylbenzene, or methyl chlorophenyl silicone oil. .
Dialkyl adipate lubricants preparation using tantalum (V) halide/oxide-inorganic oxide catalysts
Dialkyl adipate lubricants preparation using tantalum (V) halide/oxide-inorganic oxide catalysts. Johnson, Thomas H. (Shell Oil Co. , USA). U.S. US 4623748 A 18 Nov 1986, 8 pp. (United States of America) CODEN: USXXAM. CLASS: ICM: C07C067-08.There are some reagents with their cas registry numbers 16958-92-2 and 151-32-6 are used in this study. NCL: 560204000. APPLICATION: US 85-704984 25 Feb 1985. DOCUMENT TYPE: Patent CA Section: 51 (Fossil Fuels, Derivatives, and Related Products) Synthetic lubricants are manufd. by reacting propylene oligomers or butylene oligomers from the Dimersol process in the presence of a Ta (V) halide (or oxide)-inorg. oxide catalyst, converting the resulting C8-12 olefins to C9-13 alcs., and reacting the alc. with adipic acid to produce dialkyl adipates with higher flash points. Thus, a synthetic lubricant was prepd. by reacting propylene oligomer with a TaCl5-SiO2 catalyst, converting C8-12 olefins to alcs., and reacting the alcs. with adipic acid to produce dinonyl adipate, which had a flash point (ASTM D-92)) of 455°F, vs. 390°F for the adipate prepd. from conventional oxo alcs. .
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