| | Tributylamine Basic information |
| | 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 | n20/D 1.428(lit.) | | Fp | 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 | | pka | 9.99±0.50(Predicted) | | 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. | | LogP | 3.34 at 25℃ | | CAS DataBase Reference | 102-82-9(CAS DataBase Reference) | | NIST Chemistry Reference | Tributylamine(102-82-9) | | EPA Substance Registry System | Tributylamine (102-82-9) |
| | Tributylamine Usage And Synthesis |
| Chemical Properties | Pale-yellow liquid; amine odor. Slightly soluble in water; soluble in most organic
solvents. Combustible. | | Chemical Properties | Butyl amines are highly flammable, colorless
liquids (n-turns yellow on standing) with ammoniacal or fishlike odors. n-isomer: | | Uses | Solvent, inhibitor in hydraulic fluids, intermediate. | | Uses | Tributylamine is used as a solvent, an inhibitor in hydraulic fluids, a dental cement,
and in isoprene polymerization. | | Uses | Tri-n-butylamine is an important intermediate in the production of phase transfer catalysts like tributylmethylammonium chloride and tributylbenzylammonium chloride. It is also used in pharmaceuticals, agrochemicals, surfactants, lubricant additives, vulcanization accelerators and dyes. It acts as a catalyst and as a solvent in organic syntheses and polymerization reactions. It serves as a strong base anion exchanger, acid acceptor, inhibitor in hydraulic fluids and an emulsifying agent. Further, it is used to prepare photographic chemicals. | | Definition | ChEBI: Tributylamine is a tertiary amine. | | Production Methods | Tributylamine (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 Description | A 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 Reactions | Hygroscopic. Slightly soluble in water. | | Reactivity Profile | Tributylamine 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 Hazard | TOXIC; 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 Hazard | In 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 Hazard | Combustible 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 uses | TBA 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 Profile | Poison 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 Exposure | Alert: (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 | | Metabolism | Green 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. | | Shipping | UN1125 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 Methods | Purify 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.] | | Incompatibilities | May 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 Disposal | Use 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 |
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