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Diisopropyl methylphosphonate

From Wikipedia, the free encyclopedia
Not to be confused withDIMP (antiandrogen).
Diisopropyl methylphosphonate
Diisopropyl methlyphosphonate chemical structure
Diisopropyl methlyphosphonate chemical structure
Names
Preferred IUPAC name
Di(propan-2-yl) methylphosphonate
Other names
2-(Methyl-propan-2-yloxyphosphoryl)oxypropane
Identifiers
3D model (JSmol)
AbbreviationsDIMP
ChEBI
ChemSpider
ECHA InfoCard100.014.451Edit this at Wikidata
UNII
  • InChI=1S/C7H17O3P/c1-6(2)9-11(5,8)10-7(3)4/h6-7H,1-5H3
    Key: WOAFDHWYKSOANX-UHFFFAOYSA-N
  • InChI=1/C7H17O3P/c1-6(2)9-11(5,8)10-7(3)4/h6-7H,1-5H3
    Key: WOAFDHWYKSOANX-UHFFFAOYAE
  • CP(OC(C)C)(OC(C)C)=O
Properties
C7H17O3P
Molar mass180.184 g·mol−1
Density0.976 g/mL
Boiling point215 °C (419 °F; 488 K)
Hazards
Flash point98 °C (208 °F; 371 K)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Diisopropyl methylphosphonate (DIMP), also known asdiisopropyl methane-phosphonate andphosphonic acid and methyl-bis-(1-methylethyl)ester, is a chemical by-product in the production ofsarin gas when two equivalents ofisopropyl alcohol react withmethylphosphonyl difluoride instead of one.[1]

DIMP is a colorless liquid that has been shown to affect thehematological (blood forming) system in animals.[2] Its chemical formula isC7H17O3P.[3]

It degrades into isopropyl methylphosphonic acid.[1]

History

[edit]

DIMP is a chemical by-product resulted from the manufacture of sarin (GB).[1]

Use

[edit]

No commercial uses of DIMP are known to exist.[4]

Occurrences

[edit]

DIMP is not known to occur naturally in the environment.[citation needed]

Productions

[edit]

Synthesis

[edit]

DIMP can be prepared by a gradual addition of triisopropyl phosphite withmethyl iodide, utilizingdistillation technique.

References

[edit]
  1. ^abc"ATSDR - Toxic Substances - Diisopropyl Methylphosphonate (DIMP)". Atsdr.cdc.gov.
  2. ^"diisopropyl methylphosphonate datasheet"(PDF). ATSDR. August 1999. tf119. Retrieved2012-10-18.
  3. ^"Center of Chemicals". Chemicals.pl. Retrieved2012-10-18.
  4. ^"4.3 USE"(PDF). TOXICOLOGICAL PROFILE FOR DIISOPROPYL METHYLPHOSPHONATE (Report). ATSDR. August 1998. p. 92.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Diisopropyl_methylphosphonate&oldid=1290423550"
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