110-63-4

  • Product Name:1,4-Butanediol
  • Molecular Formula:C4H10O2
  • Purity:99%
  • Molecular Weight:
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Product Details;

CasNo: 110-63-4

Molecular Formula: C4H10O2

Appearance: viscous colourless liquid

110-63-4 Name

Name

1,4-Butanediol

Synonym

1,4-Butandiol ,1,4-Butanediol ,Dabco BDO ,MFCD00002968 ,EINECS 203-786-5 ,Diol 14B,BDO,butane-1,4-diol,agrisynthb1d,1,4-Dihydroxybutane,1,4-Butylene Glycol,Butanediol,1,4-BD,sucolb,4-hydroxybutanol,Tetramethylene Glycol, 1,4-Butylene glycol,Tetramethylene glycol

 

110-63-4 Chemical & Physical Properties

Melting point 

20 °C

Boiling point

228.0±0.0 °C at 760 mmHg

Density

1.0±0.1 g/cm3

Molecular Formula

C4H10O2

Molecular Weight

90.121

storage temp. 

Store below +30°C.

Form and Color

Liquid,Clear colorless

Flash Point

105.9±13.0 °C

Exact Mass

90.068077

PSA

40.46000

LogP

-1.02

Vapour density

3.1 (vs air)

Vapour Pressure

0.0±1.0 mmHg at 25°C

Index of Refraction

1.441

Stability

Stable. Combustible. Incompatible with strong oxidizing agents, mineral acids, acid chlorides, acid anhydrides.

Water Solubility

Miscible

 

110-63-4 Description

1,4-butanediol (1,4-BD) is a colorless, viscous liquid derived from butane by placement of alcohol groups at each end of its molecular chain and is one of four stable isomers of butanediol.the hydroxyl function of each end group of the Butanediol reacts with different mono- and bifunctional reagents: for example with dicarboxylic acids to polyesters, with diisocyanates to polyurethanes, or with phosgene to polycarbonates. 1.4-Butanediol (BDO) is a high-quality intermediate. BDO and its derivatives are widely used for producing plastics, solvents, electronic chemicals and elastic fibers. Additionally BDO is also a building block for the synthesis of polyesterpolyols and polyetherpolyols.

 

110-63-4 Uses

  1. Butanediol and its derivatives is used in a broad spectrum of applications in the chemical industry; amongst others in the manufacturing of technical plastics, polyurethanes, solvents, electronic chemicals and elastic fibres.
  2. 1,4-Butanediol is used in the synthesis of epothilones, a new class of cancer drugs. Also used in the stereoselective synthesis of (-)-Brevisamide.
  3. 1,4-Butanediol's largest use is within tetrahydrofuran (THF) production, used to make polytetramethylene ether glycol, which goes mainly into spandex fibers, urethane elastomers, and copolyester ethers.
  4. It is commonly used as a solvent in the chemical industry to manufacture gamma-butyrolactone and elastic fibers like spandex.
  5. It is used as a cross-linking agent for thermoplastic urethanes, polyester plasticizers, paints and coatings.
  6. It undergoes dehydration in the presence of phosphoric acid yielded teterahydrofuran, which is an important solvent used for various applications.
  7. It acts an intermediate and is used to manufacture polytetramethylene ether glycol (PTMEG), polybutylene terephthalate (PBT) and polyurethane (PU).
  8. It finds application as an industrial cleaner and a glue remover.
  9. 1,4-butanediol is also used as a plasticiser (e.g. in polyesters and cellulosics), as a carrier solvent in printing ink, a cleaning agent, an adhesive (in leather, plastics, polye
  10. Butylene glycol is a solvent with good antimicrobial action. It enhances the preservative activity of parabens. Butylene glycol also serves as a humectant and viscosity controller, and to mask odor.
  11. 1,4-Butanediol is used to produce polybutyleneterephthalate, a thermoplastic polyester;and in making tetrahydrofuran, butyrolactones,and polymeric plasticizers.

 

110-63-4 Reactivity Profile

1,4-Butanediol is heat and light sensitive. 1,4-Butanediol reacts with acid chlorides, acid anhydrides and chloroformates; reacts with oxidizing agents and reducing agents. 1,4-Butanediol is incompatible with isocyanates and acids; also incompatible with peroxides, perchloric acid, sulfuric acid, hypochlorous acid, nitric acid, caustics, acetaldehyde, nitrogen peroxide and chlorine.

 

110-63-4 Safety Profile

A human poison by an unspecified route. Moderately toxic byingestion and intraperitoneal routes. Human systemic effects: altered sleep time. Combustible when exposed to heat or flame. To fight fire, use alcohol foam, mist, foam, CO2, dry chemical. Incompatible with oxidizing materials. When heated to decomposition it emits acrid smoke and fumes.

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