Dimethyldioctadecylammonium chloride information

Dimethyldioctadecylammonium chloride

Names
Preferred IUPAC name N,N-Dimethyl-N-octadecyloctadecan-1-aminium chloride
Other names Dimethyldioctadecylammonium chloride, or; Distearyl dimethyl ammonium chloride; Aliquot 207, DDAC, distearyldimonium chloride, DSDMAC
Identifiers
CAS Number	107-64-2 Y
3D model (JSmol)	Interactive image
ChemSpider	7591 Y
ECHA InfoCard	100.003.190
PubChem CID	7879
UNII	OM9573ZX3X Y
CompTox Dashboard (EPA)	DTXSID8026771
InChI InChI=1S/C38H80N.ClH/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-39(3,4)38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-2;/h5-38H2,1-4H3;1H/q+1;/p-1 Y Key: REZZEXDLIUJMMS-UHFFFAOYSA-M Y InChI=1/C38H80N.ClH/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-39(3,4)38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-2;/h5-38H2,1-4H3;1H/q+1;/p-1 Key: REZZEXDLIUJMMS-REWHXWOFAC
SMILES [Cl-].C(CCCCC[N+](C)(CCCCCCCCCCCCCCCCCC)C)CCCCCCCCCCCC
Properties
Chemical formula	C38H80ClN
Molar mass	586.52 g·mol−1
Melting point	160 °C (320 °F; 433 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

Dimethyldioctadecylammonium chloride (also commonly distearyl dimethyl ammonium chloride or distearyldimonium chloride) is an organic compound classified as quaternary ammonium salt. The nitrogen center substituted with two methyl groups and two stearyl groups. The combination of long-chain hydrocarbon groups and the cationic ammonium confers surfactant- or a detergent-like properties. For professional use only, it can be found in many wares-and-equipment sanitizers as well as cleaner/sanitizer combinations that are standard in the foodservice industry – it was once a major component of fabric softeners, but has been largely phased out because of its low biodegradability.^[1] In household products, it may also be found as an ingredient in cosmetics and hair conditioners in which it is added primarily for its antistatic effects.^[2] It is also used in organic synthesis as a phase transfer catalyst to increase reaction rates in a two-phase organic-water system.