Svoboda | Graniru | BBC Russia | Golosameriki | Facebook

To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

How to transfigure the Wikipedia

Would you like Wikipedia to always look as professional and up-to-date? We have created a browser extension. It will enhance any encyclopedic page you visit with the magic of the WIKI 2 technology.

Try it — you can delete it anytime.

Install in 5 seconds
4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
Great Wikipedia has got greater.
.
Leo
Newton
Brights
Milds

Dipropylene glycol

From Wikipedia, the free encyclopedia

Dipropylene glycol
Names
IUPAC names
4-Oxa-2,6-heptandiol and
4-Oxa-1,6-heptandiol
Other names
1,1'-Oxybis(1-propanol) and
1,1'-Oxybis(2-propanol)
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.042.504 Edit this at Wikidata
EC Number
  • 219-251-4
UNII
  • InChI=1S/2C6H14O3/c1-5(7)3-9-4-6(2)8;1-3-5(7)9-6(8)4-2/h2*5-8H,3-4H2,1-2H3 checkY
    Key: ZWHXRCBKXVJADE-UHFFFAOYSA-N checkY
  • InChI=1/2C6H14O3/c1-5(7)3-9-4-6(2)8;1-3-5(7)9-6(8)4-2/h2*5-8H,3-4H2,1-2H3
    Key: ZWHXRCBKXVJADE-UHFFFAOYAU
  • 4-oxa-2,6-heptandiol: InChI=1S/C6H14O3/c1-3-5(7)9-6(8)4-2/h5-8H,3-4H2,1-2H3
    Key: QYSXYAURTRCDJU-UHFFFAOYSA-N
  • OCCCOCCCO
  • 4-oxa-2,6-heptandiol: CC(O)COCC(C)O
Properties
C6H14O3
Molar mass 134.173 g/mol
Appearance colorless liquid
Density 1.0206 g/cm3 at 20 °C
Boiling point 230.5 °C (446.9 °F; 503.6 K)[1]
Miscible
Solubility Soluble in ethanol
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
1
0
Flash point 121 °C (250 °F; 394 K)
310 °C (590 °F; 583 K)
Safety data sheet (SDS) SIRI.org
Related compounds
Related compounds
 Ethylene glycol
Propylene glycol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Dipropylene glycol is a mixture of three isomeric chemical compounds, 4-oxa-2,6-heptandiol, 2-(2-hydroxy-propoxy)-propan-1-ol, and 2-(2-hydroxy-1-methyl-ethoxy)-propan-1-ol. It is a colorless, nearly odorless liquid with a high boiling point and low toxicity.[2][3]

YouTube Encyclopedic

  • 1/3
    Views:
    23 020
    72 538
    6 816
  • DPG Dipropylene Glycol for incense making
  • Is Propylene Glycol a disinfectant?
  • PROPYLENE GLYCOL: ANTIFREEZE in COSMETICS?

Transcription

Uses

Dipropylene glycol finds many uses as a plasticizer, an intermediate in industrial chemical reactions, as a polymerization initiator or monomer, and as a solvent. Its low toxicity and solvent properties make it an ideal additive for perfumes and skin and hair care products. It is also a common ingredient in commercial fog fluid, used in entertainment industry fog machines.[2][3][4]

References

  1. ^ Lide, David R. (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, Florida: CRC Press. p. 342. ISBN 0-8493-0594-2.
  2. ^ a b "Dipropylene Glycol Regular Grade (DPG)". Dow Chemical. Archived from the original on 2009-03-15. Retrieved 2009-04-07.
  3. ^ a b Lloyd R. Whittington, ed. (1993). Whittington's Dictionary of Plastics (3 ed.). Technomic Publishing. p. 138. ISBN 1-56676-090-9. Retrieved 2009-04-07.
  4. ^ "Dipropylene Glycol LO+ (DPG LO+)". Dow Chemical. Archived from the original on 2009-06-19. Retrieved 2009-04-07.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

This page was last edited on 1 September 2022, at 02:03
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.
Contact WIKI 2
Introduction
Terms of Service
Privacy Policy