Trimethylolpropane Property

Melting point:

56-58 °C(lit.)

Boiling point:

159-161 °C2 mm Hg(lit.)

Density 

1.176

vapor density 

4.8 (vs air)

vapor pressure 

<1 mm Hg ( 20 °C)

refractive index 

1.4850 (estimate)

Flash point:

172 °C

storage temp. 

Store below +30°C.

solubility 

H₂O: 0.1 g/mL, clear

pka

14.01±0.10(Predicted)

form 

Flakes

color 

White

PH

6.5 (100g/l, H2O, 20℃)(External MSDS)

explosive limit

2-11.8%(V)

Water Solubility 

soluble

BRN 

1698309

InChIKey

ZJCCRDAZUWHFQH-UHFFFAOYSA-N

LogP

-0.975 (est)

CAS DataBase Reference

77-99-6(CAS DataBase Reference)

NIST Chemistry Reference

1,3-Propanediol, 2-ethyl-2-(hydroxymethyl)-(77-99-6)

EPA Substance Registry System

Trimethylolpropane (77-99-6)

Safety

Safety Statements 

22-24/25

WGK Germany 

1

RTECS 

TY6470000

Autoignition Temperature

375 °C DIN 51794

TSCA 

Yes

HS Code 

29054100

Hazardous Substances Data

77-99-6(Hazardous Substances Data)

Toxicity

LD50 orally in Rabbit: > 2500 mg/kg

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

P501Dispose of contents/container to..…

Trimethylolpropane Chemical Properties,Usage,Production

Chemical Properties

Trimethylolpropane is a Colorless, hygroscopic crystals. Soluble in water and alcohol. Combustible.The three primary hydroxyl groups undergo the normal OH group reactions.

Uses

Trimethylolpropane acts as a precursor to alkyd resins, high-gloss coatings and ion exchange resins. It is also employed as a multifunctional monomer utilized for the production of coatings, ethoxylated and propoxylated trimethylolpropane derivatives. Further, it serves as a building block in the polymer industry.

Application

Trimethylolpropane is used in saturated polyesters for coil coatings, alkyds for paints, polyurethanes for coatings and elastomers, acrylic acid esters for radiation curing, esters for synthetic lubricants, rosin esters and for surface treatment of pigments.
Large quantities of trimethylolpropane and its ethoxylated derivatives are used as precursors for urethanes and polyester resins. Another important field of application is in medium-oil and short-oil alkyd resins (→ Alkyd Resins). The resulting lacquers are characterized by excellent resistance to alkali, detergents, and water, combined with outstanding impact resistance and flexibility, as well as excellent clearness and clearness retention.

Definition

ChEBI: Trimethylolpropane is a primary alcohol. It is used as a precursor for the manufacture of resins including alkyds, saturated polyesters and polyurethanes (polyester polyol and polycarbonate diol).

Synthesis

Trimethylolpropane is made by the base-catalyzed aldol addition of butyraldehyde with formaldehyde followed by Cannizzaro reaction of the intermediate 2,2-bis(hydroxymethyl) butanal with additional formaldehyde and at least a stoichiometric quantity of base.

Purification Methods

Various procedures have been suggested for separating the trimethylolpropane from the formate. For instance, the concentrated reaction solution can be extracted with an organic solvent, which is then evaporated and the crude trimethylolpropane is purifified by vacuum distillation. In another variant, the aqueous reaction solution is evaporated until most of the sodium formate crystallizes and is removed by hot fifiltration. The application of electrodialysis has also been suggested. The liquid trimethylolpropane which remains is liberated of residual salts with an ion exchanger and then distilled. The removal of discoloring impurities is described in. Cyclic diethers of the acetal type (1,3-dioxanes, formals) can be converted into TMP and methanol by metal-catalyzed hydrogenation. Removal of high boiling acetals by acid treatment has been described.

Purification Methods

Crystallise it from acetone and ether and it distils at high vacuum. [Beilstein 1 III 2349.]