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ChemicalBook >  Product Catalog >  Organic Chemistry >  Alcohols,Phenols,Phenol alcohols >  Acyclic alcohols >  2,2-Dimethyl-1,3-propanediol

2,2-Dimethyl-1,3-propanediol

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2,2-Dimethyl-1,3-propanediol Basic information
2,2-Dimethyl-1,3-propanediol Chemical Properties
  • Melting point:126-128 °C
  • Boiling point:208 °C
  • Density 1.06
  • vapor density 3.6 (vs air)
  • vapor pressure <0.8 mm Hg ( 20 °C)
  • refractive index 1.4406 (estimate)
  • Flash point:107 °C
  • storage temp. Store below +30°C.
  • solubility 830g/l
  • pka14.57±0.10(Predicted)
  • form Crystalline Chunks
  • color White
  • explosive limit1.34%, 149°F
  • Water Solubility 830 g/L (20 ºC)
  • Sensitive Hygroscopic
  • Merck 14,6458
  • BRN 605291
  • Stability:Stable. Incompatible with strong oxidizing agents, acetic anhydride, acid chlorides, moisture. Combustible.
  • CAS DataBase Reference126-30-7(CAS DataBase Reference)
  • NIST Chemistry Reference1,3-Propanediol, 2,2-dimethyl-(126-30-7)
  • EPA Substance Registry SystemNeopentyl glycol (126-30-7)
Safety Information
  • Hazard Codes Xi
  • Risk Statements 36/37/38-36-41
  • Safety Statements 26-36-39
  • WGK Germany 1
  • RTECS TY5775000
  • 3
  • Autoignition Temperature750 °F
  • TSCA Yes
  • HS Code 29053990
MSDS
2,2-Dimethyl-1,3-propanediol Usage And Synthesis
  • Chemical StructureThe chemical formula for Neopentyl glycol (NPG) is C5H12O2, and it is a propane-1,3-diol carrying two methyl groups at position 2.Neopentyl glycol is soluble in water, benzene, chloroform, and very soluble in ethanol and diethyl ether. Neopentylglycol (NPG) is a unique polyalcohol offering superior performance advantages in many end-use applications due to its high chemical and thermal stability. It is a unique diol offering superior performance advantages in many end-use applications. These advantages are derived from its chemical structure. The location of the hydroxyl groups on primary carbon atoms allows rapid esterification. Additionally, the two methyl groups, instead of the usual two hydrogen atoms, on the alpha carbon atom are responsible for the high chemical and thermal stability of Neopentylglycol and its derivatives.
  • ApplicationNeopentyl glycol is used in the synthesis of polyesters, paints, lubricants, and plasticizers. When used in the manufacture of polyesters, it enhances the stability of the product towards heat, light, and water. By esterification reaction with fatty or carboxylic acids, synthetic lubricating esters with reduced potential for oxidation or hydrolysis, compared to natural esters, can be produced. NPG is used primarily in base resins for coatings. In powder coating formulations, Neopentylglycol offers the additional advantage of providing small differences between the glass transition temperature and melting point. Important areas of application include general metal, appliance, metal furniture, automotive and machinery coatings. Important uses are also found in hydraulic fluids, synthetic lubricant oils, greases, metalworking fluids and aircraft engine lubricants. Other outlets include textiles, pharmaceuticals, pesticides, plasticizers and petroleum.
    High quality NPG is shipped as flake, molten and slurry. The high-quality NPG is the component in polyester resins for industrial coatings and fiberglass-reinforced plastics applications, and most polyester resin formulations contain NPG as the sole glycol component, or it is used in conjunction with a modifying glycol to achieve desired properties. NPG is also used in polyester polyols for polyurethane coatings for the automotive, industrial maintenance, transportation, and aerospace markets.
  • Chemical Propertieswhite solid
  • UsesNPG Glycol is used in the synthesis of tetraphenylporphyrins. Also used in the synthesis of Bryostatin 2, a protein kinase modulator.
  • UsesIn the manufacture of plasticizers, polyesters, as modifier of alkyd resins.
  • General DescriptionWhite crystalline solid. Melting point 130°C.
  • Air & Water ReactionsSoluble in water.
  • Reactivity Profile2,2-Dimethyl-1,3-propanediol may generate toxic gases in combination of with alkali metals, nitrides, and strong reducing agents. Reacts with inorganic acids and carboxylic acids to form esters plus water. Converted to aldehydes or acids by oxidizing agents. May initiate the polymerization of isocyanates and epoxides.
  • Health HazardMay be harmful by ingestion or skin absorption. Causes eye and skin irritation. Material is irritating to mucous membrane and upper respiratory tract. INHALATION: Call for medical aid. Remove to fresh air. If breathing has stopped, give artificial respiration. If breathing is difficult, give oxygen.
  • Fire HazardSpecial Hazards of Combustion Products: Emits toxic fumes under fire condition.
  • Purification MethodsCrystallise the diol from *benzene or acetone/water (1:1). [Beilstein 1 IV 2551.]
2,2-Dimethyl-1,3-propanediol Preparation Products And Raw materials
2,2-Dimethyl-1,3-propanediol(126-30-7)Related Product Information
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