ChemicalBook > Product Catalog > Organic Chemistry > Amides > Acyclic polyamines and their derivatives > Tributylamine
Tributylamine Chemical Properties
- Melting point:−70 °C(lit.)
- Boiling point:216 °C(lit.)
- Density 0.778 g/mL at 25 °C(lit.)
- vapor density 6.38 (vs air)
- vapor pressure 0.3 mm Hg ( 20 °C)
- refractive index n
- Flash point:146 °F
- storage temp. Store at RT.
- solubility sparingly soluble in water; soluble in most organic solvents; soluble in acetone and benzene; very soluble in alcohol and ether
- form Liquid
- color Clear
- Water Solubility 0.386 g/L (25 ºC)
- Sensitive Hygroscopic
- Merck 14,9618
- BRN 1698872
- Stability:Stable. Combustible. Incompatible with strong oxidizing agents, strong acids. Hygroscopic.
- CAS DataBase Reference102-82-9(CAS DataBase Reference)
- NIST Chemistry ReferenceTributylamine(102-82-9)
- EPA Substance Registry SystemTributylamine (102-82-9)
Tributylamine Usage And Synthesis
- Chemical PropertiesPale-yellow liquid; amine odor. Slightly soluble in water; soluble in most organic solvents. Combustible.
- Chemical PropertiesButyl amines are highly flammable, colorless liquids (n-turns yellow on standing) with ammoniacal or fishlike odors. n-isomer:
- UsesSolvent, inhibitor in hydraulic fluids, intermediate.
- UsesTributylamine is used as a solvent, an inhibitor in hydraulic fluids, a dental cement, and in isoprene polymerization.
- Production MethodsTributylamine (TBA) is manufactured by vapor phase alkylation of ammonia with butanol to produce a technical grade compound (Windholz et al 1983).
- Synthesis Reference(s)The Journal of Organic Chemistry, 46, p. 1759, 1981 DOI: 10.1021/jo00321a056
Synthesis, p. 324, 1996
- General DescriptionA pale yellow liquid with an ammonia-like odor. Less dense than water. Very irritating to skin, mucous membranes, and eyes. May be toxic by skin absorption. Low toxicity. Used as an inhibitor in hydraulic fluids.
- Air & Water ReactionsHygroscopic. Slightly soluble in water.
- Reactivity ProfileTributylamine can react with oxidizing materials . Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
- Health HazardTOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
- Health HazardIn an occupational setting, humans are primarily exposed to TBA by the inhalation or dermal routes (HSDB 1988). TBA is poisonous when inhaled or ingested, acting as an alkaline corrosive agent. Vapors can cause irritation of the nose and throat, distressed breathing and coughing (NFPA 1986). Pneumonia and bronchitis may follow if respiratory tract infection ensues. Inhalation or ingestion of TBA has been found to cause harmful esophageal burns with the risk of perforation (HSDB 1988). Direct contact can cause secondary burns (NFPA 1986).
- Fire HazardCombustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.
- Industrial usesTBA is used as a solvent, an inhibitor in hydraulic fluids and a chemical intermediate. It is also used as a catalyst in a wide range of chemical reactions, as an insecticide, an emulsifying agent and in dental cements (HSDB 1988).
- Safety ProfilePoison by ingestion, inhalation, skin contact, and subcutaneous routes. A central nervous system stimulant, irritant, and sensitizer. A corrosive irritant to skin, eyes, and mucous membranes. Flammable when exposed to heat, flame, or oxidmers. Can react with oxidizing materials. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits toxic fumes of NOx. See also AMINES.
- Potential ExposureAlert: (n-isomer): Possible risk of forming tumors, suspected of causing genetic defects, suspected reprotoxic hazard, Primary irritant (w/o allergic reaction), (sec-isomer): Drug. n-Butylamine is used in pharmaceuticals; dyestuffs, rubber, chemicals, emulsifying agents; photography, desizing agents for textiles; pesticides, and synthetic agents. sec-Butylamine is used as a fungistate. tert-Butylamine is used as a chemical intermediate in the production of tert-Butylaminoethyl methacrylate (a lube oil additive); as an intermediate in the production of rubber and in rust preventatives and emulsion deterrents in petroleum products. It is used in the manufacture of several drugs
- MetabolismGreen and Large (1984) suggest that TBA is oxidized by a tertiary amine monooxygenase. The amine monooxygenases, located in the smooth endoplasmic reticulum, attack the amine group to give rise to the corresponding aldehyde product.
- ShippingUN1125 n-Butylamine, Hazard Class: 3; Labels: 3—Flammable liquid, 8—Corrosive material. UN2014 Isobutylamine, Hazard Class: 3; Labels: 3—Flammable liquid, 8—Corrosive material
- Purification MethodsPurify the amine by fractional distillation from sodium under reduced pressure. Pegolotti and Young [J Am Chem Soc 83 3251 1961] heated the amine overnight with an equal volume of acetic anhydride, in a steam bath. The amine layer was separated and heated with water for 2hours on the steam bath (to hydrolyse any remaining acetic anhydride). The solution was cooled, solid K2CO3 was added to neutralize any acetic acid that had been formed, and the amine was separated, dried (K2CO3) and distilled at 44mm pressure. Davis and Nakshbendi [J Am Chem Soc 84 2085 1926] treated the amine with one-eighth of its weight of benzenesulfonyl chloride in aqueous 15% NaOH at 0-5o. The mixture was shaken intermittently and allowed to warm to room temperature. After a day, the amine layer was washed with aqueous NaOH, then water and dried with KOH. (This treatment removes primary and secondary amines.) It was further dried with CaH2 and distilled under vacuum. [Beilstein 4 IV 554.]
- IncompatibilitiesMay form explosive mixture with air. May accumulate static electrical charges, and may causeignition of its vapors. n-Butylamine is a weak base; reacts with strong oxidizers and acids, causing fire and explosion hazard. Incompatible with organic anhydrides; isocyanates, vinyl acetate; acrylates, substituted allyls; alkylene oxides; epichlorohydrin, ketones, aldehydes, alcohols, glycols, phenols, cresols, caprolactum solution. Attacks some metals in presence of moisture. The tert-isomer will attack some forms of plastics
- Waste DisposalUse a licensed professional waste disposal service to dispose of this material. Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner andscrubber. All federal, state, and local environmental regulations must be observed.
Tributylamine Preparation Products And Raw materials
- Tetraethylammonium hydrogensulfate TRI-N-HEXYLAMINE Methyl tributyl ammonium chloride TETRABUTYLAMMONIUM CHLOROCHROMATE Benzyltributylammonium bromide Tetrabutyl ammonium chloride TETRA-N-BUTYLAMMONIUM TETRAPHENYLBORATE Butylamine PERFLUORO-N-TRIBUTYLAMINE,tributylamine,heptacosafluoro Tributyl phosphate Dibutyl maleate Dibutylamine Salbutamol Loperamide Dibutyl phthalate Tributylphosphine Tributylamine Chlorotributyltin