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== External links == == External links ==
* * {{Webarchive|url=https://web.archive.org/web/20100109131018/http://msds.chem.ox.ac.uk/AD/adipoyl_chloride.html |date=2010-01-09 }}


{{Navbox acyl chlorides}} {{Navbox acyl chlorides}}

Latest revision as of 21:45, 2 August 2023

Adipoyl chloride
Skeletal formula
Skeletal formula
Names
Preferred IUPAC name Hexanedioyl dichloride
Other names Adipoyl dichloride
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference 507709
ChemSpider
ECHA InfoCard 100.003.525 Edit this at Wikidata
EC Number
  • 203-876-4
PubChem CID
UN number 3265
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C6H8Cl2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2Key: PWAXUOGZOSVGBO-UHFFFAOYSA-N
  • InChI=1/C6H8Cl2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2Key: PWAXUOGZOSVGBO-UHFFFAOYAI
SMILES
  • O=C(Cl)CCCCC(Cl)=O
Properties
Chemical formula C6H8Cl2O2
Molar mass 183.03 g·mol
Density 1.25 g/cm
Boiling point 105 to 107 °C (221 to 225 °F; 378 to 380 K) at 2 mmHg
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorusSpecial hazards (white): no code
3 1 2
Flash point 160 °C (320 °F; 433 K) (closed cup)
Related compounds
Related compounds Adipic acid
Hexanedihydrazide
Hexanedinitrile
Hexanediamide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Adipoyl chloride (or adipoyl dichloride) is the organic compound with the formula (CH2CH2C(O)Cl)2. It is a colorless liquid. It reacts with water to give adipic acid.

It is prepared by treatment of adipic acid with thionyl chloride. Adipoyl chloride reacts with hexamethylenediamine to form nylon 6,6.

See also

References

  1. P. C. Guha; D. K. Sankaran (1946). "Muconic Acid". Organic Syntheses. 26: 57–60. doi:10.15227/orgsyn.026.0057. PMID 20280761.
  2. Morgan, Paul W.; Kwolek, Stephanie L. (April 1959). "The nylon rope trick: Demonstration of condensation polymerization". J. Chem. Educ. 36 (4): 182. Bibcode:1959JChEd..36..182M. doi:10.1021/ed036p182.

External links

Diacyl chlorides (-COCl)2
Chemical structure of the -COCl group
Category:Acyl chlorides
Categories:
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