2-Methyl-2,4-pentanediol

2-Methyl-2,4-pentanediol
Names
IUPAC name
2-Methyl-2,4-pentanediol
Other names
Hexylene glycol; Diolane; 1,1,3-Trimethyltrimethylenediol; 2,4-Dihydroxy-2-methylpentane; Isol
Identifiers
107-41-5 YesY
99210-90-9 (R) N
99210-91-0 (S) N
3D model (Jmol) Interactive image
Abbreviations MPD
ChEBI CHEBI:62995 N
ChEMBL ChEMBL2104293 N
ChemSpider 7582 YesY
ECHA InfoCard 100.003.173
PubChem 7870
UNII KEH0A3F75J YesY
Properties
C6H14O2
Molar mass 118.18 g·mol−1
Appearance colourless liquid
Odor mild, sweetish[1]
Density 0.92 g/mL
Melting point −40 °C (−40 °F; 233 K)
Boiling point 197 °C (387 °F; 470 K)
miscible[1]
Vapor pressure 0.05 mmHg (20°C)[1]
Hazards
Flash point 98.3 °C (208.9 °F; 371.4 K) [2]
Explosive limits 1.3%-7.4%[1]
US health exposure limits (NIOSH):
PEL (Permissible)
 none[1]
REL (Recommended)
 C 25 ppm (125 mg/m3)[1]
IDLH (Immediate danger)
 N.D.[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

2-Methyl-2,4-pentanediol (MPD) is an organic compound with the formula (CH3)2C(OH)CH2CH(OH)CH3. This colourless liquid is a chiral diol. It is produced industrially from diacetone alcohol by hydrogenation.[3] Total European and USA production was 15000 tonnes in 2000.[4]

2-Methyl-2,4-pentanediol exists as two enantiomers, (4R)-(-) and (4S)-(+). In the Protein Data Bank, the 3-letter code "MPD" refers to the (S)-(-) enantiomer, while "MRD" is used to refer to the (R)-(+) version. Commercial products labeled "MPD" are usually the racemate,[5] also sold as and referred to as "hexylene glycol".[6][7]

Uses

2-Methyl-2,4-pentanediol exhibits both surfactant and emulsion-stabilizing properties. Its relatively high viscosity and low volatility are advantageous in coatings, cleansers, cosmetics, solvents, and hydraulic fluids.[8] Although it is an irritant at higher concentrations, It is sometimes used in skin care, hair care, soap, and eye cosmetic products at concentrations ranging from 0.1% - 25%.[9][10]

It is biodegradable and unlikely to accumulate in the environment.[11]

Laboratory uses

In the laboratory it is a common precipitant and cryoprotectant in protein crystallography.[12] Since hexylene glycol is compatible with polar and nonpolar molecules, it competes with the solvent in a crystallography experiment causing the protein to precipitate.[13] Hexylene glycol is so effective in protein crystallography because its amphiphilic nature and small, flexible structure allows it to bind to many different locations on a protein secondary structure including alpha helices and beta sheets.[14] When hexylene glycol binds to these different locations, water is removed and the protein crystals anneal, which prevents ice formation during cryocrystallography techniques.[15] Incorporation of hexylene glycol into solution has been known to improve the resolution of X-ray diffraction making protein structures easily identifiable.[16] Additionally hexylene glycol is not a strong denaturing agent and thus does not significantly alter the structure of a protein during the crystallography procedure.[14]

Like related diols, it forms borate esters.

References

  1. 1 2 3 4 5 6 7 "NIOSH Pocket Guide to Chemical Hazards #0328". National Institute for Occupational Safety and Health (NIOSH).
  2. ↑ CDC - NIOSH Pocket Guide to Chemical Hazards
  3. ↑ Stylianos Sifniades, Alan B. Levy, "Acetone" in Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. doi:10.1002/14356007.a01_079.pub3
  4. ↑ SIDS Initial Assessment Report for SIAM 13: Hexylene Glycol
  5. ↑ MPD at Hampton Research , MPD Product Page
  6. ↑ Hexylene Glycol at Sigma Aldrich , Hexylene Glycol Product Page
  7. ↑ Hexylene Glycol at Jena Bioscience, Hexylene Glycol Product Page
  8. ↑ Chemicalland21.com Hexylene glycol
  9. ↑ Kinnunen, T. (1991). "Antibacterial and antifungal properties of propylene glycol, and 1,3-butylene glycol in vitro". Acta Dermato-venereologica.
  10. ↑ R. Rietschel; J. Fowler; A. Fisher Hexylene Glycol. In Fisher's Contact Dermatitis; Holmes, M., Ed.; BC Decker Inc.: Hamilton,Ontario, 2008; pp 290
  11. ↑ Rhodia Hexylene glycol GPS Safety Summary. 2012.
  12. ↑ Crystallization Techniques: Additives, Enrico Stura, University of Glasgow
  13. ↑ Dumetz, A. (2009). "Comparative Effects of Salt, Organic and Polymer Precipitants on Protein Phase Behavior and Implications for Vapor Diffusion". J. Cryst. Growth.
  14. 1 2 Anand, K (2002). "An overview on 2-methyl-2,4-pentanediol in crystallization and in crystals of biological macromolecules". Acta Crystallogr.
  15. ↑ Viatcheslav, Berejnov (2006). "Thornea Effects of cryoprotectant concentration and cooling rate on vitrification of aqueous solutions". J. Appl. Crystallography.
  16. ↑ Vera, L (2006). "Strategies for Protein Crystallography". Cryst. Growth Des.
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