559:
39:
237:
162:
420:
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421:
581:
Due to the shock and light sensitive nature of organic peroxides, dipropyl ether should never be boiled or evaporated to dryness. This concentrates peroxides that may be present, which can then detonate unexpectedly destroying the vessel in which they have deposited or igniting nearby flammable
419:
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38:
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119:
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375:
365:
150:
640:
O'Neil, Maryadele; Heckelman, Patricia; Koch, Cherie; Roman, Kristin, eds. (2006).
529:(a strong acid) and heat, in the same way other symmetrical ethers may be formed.
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17:
443:
436:
429:
402:
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170:
498:
467:
Except where otherwise noted, data are given for materials in their
570:
As is typical of ethers, dipropyl ether may slowly form explosive
490:
118:
108:
518:
Dipropyl ether can be synthesized by reacting two molecules of
220:
414:
578:are often added to ethers to prevent this process.
574:over long periods in storage. Antioxidants such as
719:Canadian Centre for Occupational Health and Safety
182:
418:
94:
644:(14th ed.). Merck Research Laboratories.
537:This ether may also be prepared by way of the
8:
626:Institute for Occupational Safety and Health
260:InChI=1S/C6H14O/c1-3-5-7-6-4-2/h3-6H2,1-2H3
270:InChI=1/C6H14O/c1-3-5-7-6-4-2/h3-6H2,1-2H3
235:
160:
138:
26:
202:
613:
611:
609:
607:
370:−122 °C (−188 °F; 151 K)
635:
633:
603:
291:
256:
231:
151:
665:Fox, Marye; Whitesell, James (2004).
505:with a sweet odor typical of ethers.
380:90 °C (194 °F; 363 K)
263:Key: POLCUAVZOMRGSN-UHFFFAOYSA-N
7:
461:−18 °C (0 °F; 255 K)
669:. Jones & Bartlett Publishers.
273:Key: POLCUAVZOMRGSN-UHFFFAOYAT
173:
642:Merck Index of Chemicals and Drugs
545:-propoxide, the conjugate base of
25:
557:
321:
37:
691:"Diethyl ether product listing"
471:(at 25 °C , 100 kPa).
549:-propanol, is reacted with an
514:Acid catalyzed ether synthesis
327:
315:
1:
67:Dipropyl ether, normal isomer
501:groups. It is a colorless,
771:
715:"Organic peroxide hazards"
539:Williamson ether synthesis
533:Williamson ether synthesis
667:Organic Chemistry, 3rd ed
622:GESTIS Substance Database
465:
396:
302:
282:
247:
78:
62:
50:
45:
36:
755:Sweet-smelling chemicals
576:butylated hydroxytoluene
527:p-toluenesulfonic acid
425:
424:
407:(fire diamond)
52:Preferred IUPAC name
525:in the presence of
489:is the symmetrical
387:Solubility in water
342: g·mol
33:
750:Symmetrical ethers
475:Infobox references
426:
27:
651:978-0-911910-00-1
592:Diisopropyl ether
572:organic peroxides
483:Chemical compound
481:
480:
350:Colorless liquid
216:CompTox Dashboard
120:Interactive image
65:Propyl ether, di-
16:(Redirected from
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553:-propyl halide:
503:flammable liquid
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310:Chemical formula
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56:1-Propoxypropane
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745:Dialkyl ethers
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676:978-0763735869
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487:Dipropyl ether
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469:standard state
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392:3 g/L (20 °C)
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32:-propyl ether
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18:Dipropyl ether
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695:Sigma-Aldrich
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376:Boiling point
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73:-propyl ether
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722:. Retrieved
709:
698:. Retrieved
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546:
542:
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520:
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494:
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403:
79:Identifiers
70:
63:Other names
29:
509:Preparation
457:Flash point
347:Appearance
303:Properties
158:100.003.518
739:Categories
724:2012-07-03
700:2012-07-03
598:References
360:0.75 g/cm
335:Molar mass
204:42Q250HS4G
131:ChemSpider
107:3D model (
86:CAS Number
582:liquids.
541:in which
523:-propanol
294:O(CCC)CCC
586:See also
404:NFPA 704
397:Hazards
96:111-43-3
624:of the
620:in the
618:Record
493:of two
356:Density
340:102.177
171:PubChem
673:
648:
566:Safety
499:propyl
287:SMILES
46:Names
491:ether
252:InChI
109:JSmol
671:ISBN
646:ISBN
195:UNII
184:8114
140:7823
221:EPA
174:CID
69:Di-
28:Di-
741::
717:.
693:.
632:^
606:^
325:14
727:.
703:.
679:.
654:.
551:n
547:n
543:n
521:n
497:-
495:n
445:1
438:3
431:1
328:O
322:H
319:6
316:C
223:)
219:(
111:)
71:n
30:n
20:)
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