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Dibutylamine

CAS No.
111-92-2
Chemical Name:
Dibutylamine
Synonyms
DI-N-BUTYLAMINE;DNBA;Dibutylamin;Dibuthylamine;N-DIBUTYLAMINE;N-BUTYL-1-BUTANAMINE;ai3-52649;ai3-15329;(n-C4H9)2NH;Dibutilamina
CBNumber:
CB8416375
Molecular Formula:
C8H19N
Molecular Weight:
129.24
MDL Number:
MFCD00009429
MOL File:
111-92-2.mol
MSDS File:
SDS
Last updated:2024-03-14 15:18:27

Dibutylamine Properties

Melting point −62 °C(lit.)
Boiling point 159 °C(lit.)
Density 0.767 g/mL at 25 °C(lit.)
vapor density 4.46 (vs air)
vapor pressure 1.9 mm Hg ( 20 °C)
refractive index n20/D 1.417(lit.)
Flash point 106 °F
storage temp. Store below +30°C.
solubility water: soluble3.8g/L at 20°C
pka 11.25(at 21℃)
form Liquid
color White
PH 11.1 (1g/l, H2O, 20℃)
Odor Weak ammonia.
explosive limit 0.6-6.8%(V)
Water Solubility 4.05 g/L (25 ºC)
Merck 14,3032
BRN 506001
Dielectric constant 3.0(20℃)
Stability Stable. Combustible. Incompatible with strong oxidizing agents, most common metals, strong acids. Vapours may flow over surfaces to a distant source of ignition. Can form explosive mixtures with air.
InChIKey JQVDAXLFBXTEQA-UHFFFAOYSA-N
LogP 2.1 at 23℃
CAS DataBase Reference 111-92-2(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 2194M2LA21
NIST Chemistry Reference 1-Butanamine, N-butyl-(111-92-2)
EPA Substance Registry System Dibutylamine (111-92-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS05,GHS06
Signal word  Danger
Hazard statements  H226-H302-H311-H314-H330
Precautionary statements  P210-P280-P301+P312-P303+P361+P353-P304+P340+P310-P305+P351+P338
Hazard Codes  Xn,T
Risk Statements  10-20/21/22-35-23-21/22
Safety Statements  45-36/37/39-28A-26-23
RIDADR  UN 2248 8/PG 2
WGK Germany  1
RTECS  HR7780000
10
Autoignition Temperature 594 °F
TSCA  Yes
HS Code  2921 19 99
HazardClass  8
PackingGroup  II
Toxicity LD50 orally in rats: 550 mg/kg (Smyth)
NFPA 704
2
3 0

Dibutylamine price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.03222 Dibutylamine for synthesis 111-92-2 100mL $36.9 2024-03-01 Buy
Sigma-Aldrich 8.03222 Dibutylamine for synthesis 111-92-2 1L $54.9 2024-03-01 Buy
Sigma-Aldrich 8.03222 Dibutylamine for synthesis 111-92-2 2.5L $96.1 2024-03-01 Buy
Sigma-Aldrich 8.03222 Dibutylamine for synthesis 111-92-2 40kg $948 2024-03-01 Buy
Sigma-Aldrich 471232 Dibutylamine ≥99.5% 111-92-2 1l $88 2024-03-01 Buy
Product number Packaging Price Buy
8.03222 100mL $36.9 Buy
8.03222 1L $54.9 Buy
8.03222 2.5L $96.1 Buy
8.03222 40kg $948 Buy
471232 1l $88 Buy

Dibutylamine Chemical Properties,Uses,Production

Description

Dibutylamine is a colorless liquid with anodor of ammonia. Molecular weight = 129.28; Boilingpoint = 159-161℃; Freezing/Melting point = - 61.9 to259℃; Flash point = 42-47℃; Autoignitiontemperature = 260℃. Explosive Limits: LEL = 1.1%;UEL—unknown. Hazard Identification (based on NFPA704 M Rating System): Health 3, Flammability 2,Reactivity 0. Slightly soluble in water.

Chemical Properties

n-Dibutylamine is a strong base and undergoes reactions with acids. It reacts with carbon disulfide and carbon dioxide to form alkyl ammonium salts of dithiocarbamic acid and carbamic acid, respectively.
n-Dibutylamine is nitrosated by nitrite at low pHs to form the mutagenic and carcinogenic product, N-nitrosodibutylamine (Sithole and Guy 1986).

Chemical Properties

Dibutylamine is a colorless liquid with an odor of ammonia.

Uses

Dibutylamine was employed as organocatalyst during the synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates via Knoevenagel, Pinner and phospha-Michael reactions. Di-n-butylamine (Dibutylamine) may be used to investigate the performance of a dry sampler, with an impregnated denuder in series with a glass fibre filter for airborne isocyanates. It was used in the preparation of 1M dibutylammonium phosphate buffer.

Uses

Dibutylamine is a secondary dialkylamine. It is a versatile intermediate with a variety of applications.
Dibutylamine is extensively used in palladium-catalyzed cross-coupling with aryl halides to synthesize arylamines, popularly known as Buchwald–Hartwig amination.
It can be used in the oxone-mediated annulation of 2-aminobenzamides and 1,2-diaminobenzenes to synthesize 2,3-dihydroquinazolin-4(1H)-ones and 1H-benzimidazoles, respectively.
It can also be used in the one-pot multicomponent reactions to synthesize tetra- and penta-substituted polyfunctional dihydropyrroles.
Dibutylamine was employed as organocatalyst during the synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates via Knoevenagel, Pinner and phospha-Michael reactions. Di-n-butylamine (Dibutylamine) may be used to investigate the performance of a dry sampler, with an impregnated denuder in series with a glass fibre filter for airborne isocyanates. It was used in the preparation of 1M dibutylammonium phosphate buffer.

Production Methods

n-Dibutylamine is prepared by two major methods. The first involves passing ammonia and butanol over an alumina or silica catalyst at a temperature of 300-500°C and under pressure. The second method employs passing ammonia, butanol, and hydrogen over a dehydrogenation catalyst. In each instance the resulting mixtures are separated by continuous distillation and extraction (Schweizer et al 1978). n-Dibutylamine can also be prepared from butyl bromide and ammonia or by reaction of butyl chloride and ammonia (HSDB 1989). The amine also is naturally present in food (Neurath et al 1977) and its emissions are produced in soil and sewage. The amine is also found in the expired air of normal, healthy, nonsmoking adults (Krotoszynski et al 1979).
N-Nitrosamines and their precursors including n-dibutylamine are present in rubber products in which the accelerators and stabilizers used in the vulcanization process were derived from dialkylamines. Analysis of a single extraction of rubber nipples and baby pacifiers with artificial saliva (containing sodium nitrite) showed n-dibutylamine levels up to 3890 p.p.b. and N-nitrosodibutylamine concentrations as high as 427 p.p.b. (Thompson et al 1984).

General Description

A yellow-colored liquid with a amine-like odor. Denser than water. Very corrosive, may burn skin, eyes, and mucous membranes. Flash point 125°F. Combustible. Produce toxic oxides of nitrogen when burned. Used to make other chemicals.

Air & Water Reactions

Flammable. Soluble in water.

Reactivity Profile

Dibutylamine 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

n-Dibutylamine is a severe irritant to skin and mucous membranes of the nose, eyes, and respiratory tract. Exposure to this amine may result in some activation of the sympathetic branch of the autonomic nervous system as manifested by elevated blood pressure, eye pupil dilation and flushing of the skin.

Fire Hazard

Special Hazards of Combustion Products: Toxic oxides of nitrogen may form in fires.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: May corrode some metals and attack some forms of plastics; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Industrial uses

Primary industrial uses of n-dibutylamine include flotation reagents, dyestuffs, rubber vulcanization accelerators, and corrosion inhibitors (HSDB 1989). In 1985 US production totalled approximately 2000 tons.

Safety Profile

Poison by ingestion and subcutaneous routes. Moderately toxic by skin contact and inhalation. Corrosive. A severe skin and eye irritant. Mutation data reported. Flammable liquid when exposed to heat or flame; can react with oxidizing materials. To fight fire, use alcohol foam, foam, CO2, dry chemical. Exothermic reaction with cellulose nitrate does not proceed to ignition. When heated to decomposition it emits toxic fumes of NOx.

Potential Exposure

Used as a corrosion inhibitor; and intermediate for emulsifiers, rubber products, dyes; and insecticides.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. If victim is conscious, administer water ormilk. Do not induce vomiting. Medical observation isrecommended for 2448 h after breathing overexposure, aspulmonary edema may be delayed. As first aid for pulmonary edema, a doctor or authorized paramedic may consideradministering a corticosteroid spray.

Metabolism

There is little information available on the absorption, distribution and metabolism of ra-dibutylamine. Aliphatic amines such as dibutylamine are well absorbed from the gut. Both monoamine oxidase and diamine oxidase, which are present in most tissues, are capable of metabolizing many exogenous amines. Although the metabolism of primary amines is more rapid than secondary, the rate of oxidation by the enzyme increases with chain length of the amine, reaching a maximum of five carbon atoms (Beard and Noe 1981). Therefore, n-dibutylamine may be metabolized by these enzyme systems although definitive evidence is lacking.
The highly carcinogenic and mutagenic N-nitrosodibutylamine is formed by reaction of nitrite with n-dibutylamine, the highest rates of nitrosation occurring at low pH (Sithole and Guy 1986). The n-dibutylamine present in ingested foods is nitrosated in the stomach by endogenous nitrite from saliva, etc. together with the sodium nitrite present in some preserved foods to form the highly toxic Nnitrosamine (Airoldi et al 1987). Food additives such as butylated hydroxyanisole inhibited in vitro the nitrosation of n-dibutylamine but this inhibition was not seen in vivo in rats that were given both n-dibutylamine and sodium nitrite.
The endogenous formation of N-nitrosodibutylamine was studied in rats after administration of sodium nitrite or sodium nitrate and n-dibutylamine (Airoldi et al 1984). Urinary excretion of N-nitrosodibutylamine and its metabolites N-butyl- N-(4-hydroxybutyl)-nitrosamine (BBN) and N-butyl-N-(3-carboxypropyl)nitrosamine (BCPN) than was determined. Rats were supplied with 0.2% sodium nitrite or 0.5% sodium nitrate in drinking water and given n-dibutylamine by gavage at 3 doses of 50 mg/kg, 8 h apart. Analysis of the 24 h urine by GC equipped with a thermal energy analyzer failed to detect N-nitrosodibutylamine or its metabolite BBN. However, BCPN was found in the urine of both the sodium nitrite and sodium nitrate groups, indicating that in vivo nitrosation of n-dibutylamine had occurred.

storage

Color Code—White: Corrosive or Contact Hazard;Store separately in a corrosion-resistant location. Prior toworking with dibutylamine you should be trained on itsproper handling and storage. Before entering confined spacewhere this chemical may be present, check to make surethat an explosive concentration does not exist. Store intightly closed containers in a cool, well-ventilated areaaway from incompatible materials listed above. Metal containers involving the transfer of this chemical should begrounded and bonded. Where possible, automatically pumpliquid from drums or other storage containers to processcontainers. Drums must be equipped with self-closingvalves, pressure vacuum bungs, and flame arresters. Useonly nonsparking tools and equipment, especially whenopening and closing containers of this chemical. Sources ofignition, such as smoking and open flames, are prohibitedwhere this chemical is used, handled, or stored in a mannerthat could create a potential fire or explosion hazard.Wherever this chemical is used, handled, manufactured, orstored, use explosion-proof electrical equipment andfittings.

Shipping

UN2248 Di-n-butylamine, Hazard class: 8; Labels: 8-Corrosive material, 3-Flammable liquid.

Purification Methods

Dry this strong base with LiAlH4, CaH2 or KOH pellets, filter and distil it from BaO or CaH2. [Beilstein 4 IV 550.]

Toxicity evaluation

Animal studies have demonstrated that dibutylamine is severely irritating to the eyes. An acute oral rat LD50 value of 550 mg/kg has been reported. The 4 h LC50 in rats is 1150 mg/m3. The 1 h LC50 in rats is >557 ppm.
In a 90 day exposure of rats to 0, 50, 150, or 450 mg/m3, resulted in nasal metaplasia as well as a form of mucous cell hyperplasia.

Incompatibilities

May form explosive mixture with air. Aqueous solution is a strong base. Incompatible with acids, acid chlorides; acid anhydrides; halogens, isocyanates, vinyl acetate; acrylates, substituted allyls; alkylene oxides, epichlorohydrin, ketones, aldehydes, alcohols, gly- cols, phenols, cresols, caprolactum solution; strong oxidi- zers; reactive organic compounds. Attacks copper alloys, zinc, tin, tin alloys; galvanized steel. Also, carbon dioxide is listed as incompatible by the state of New Jersey.

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

6287-40-7
111-92-2
Synthesis of Dibutylamine from DIBUTYLAMINE HYDROCHLORIDE
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View Lastest Price from Dibutylamine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Dibutylamine pictures 2024-11-04 Dibutylamine
111-92-2
US $2.00 / KG 1KG 99% 1000mt/year Jinan Finer Chemical Co., Ltd
Dibutylamine pictures 2024-10-24 Dibutylamine
111-92-2
US $15.00 / kg 5kg 99% 300tons Hebei Dangtong Import and export Co LTD
Dibutylamine pictures 2023-06-20 Dibutylamine
111-92-2
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
  • Dibutylamine pictures
  • Dibutylamine
    111-92-2
  • US $2.00 / KG
  • 99%
  • Jinan Finer Chemical Co., Ltd
  • Dibutylamine pictures
  • Dibutylamine
    111-92-2
  • US $15.00 / kg
  • 99%
  • Hebei Dangtong Import and export Co LTD
  • Dibutylamine pictures
  • Dibutylamine
    111-92-2
  • US $0.00 / KG
  • 99%
  • Hebei Mojin Biotechnology Co., Ltd
(n-C4H9)2NH 1-Butanamine,N-butyl- ai3-15329 ai3-52649 butanamine,N-butyl Butylamine, di-N- Dibutilamina DIBUTYLAMINE, 98+% N-BUTYLDIETHANOLAMINE, 98.6+% 2,5-DICHLOROANILINE PESTANAL Dibutylamine,Certified DibutylamineForSynthesis Di-n-butylamine, 98+% Di-n-butylamine, 99.5% DI-n-BUTYLAMINE, 99+% N-BUTYL BUTANAMINE DI-N-AMYLAMINE di-n-butylamine, N-butyl butanamine n-Dibutylamine N-Butyl-1-butanamine DIBUTYLAMINE FOR SYNTHESIS 100 ML DIBUTYLAMINE FOR SYNTHESIS 40 KG DIBUTYLAMINE FOR SYNTHESIS 1 L DIBUTYLAMINE FOR SYNTHESIS 2,5 L DI-N-BUTYLAMINE, FOR HPLC 1,1'-Iminobisbutane Di-n-butylamin di-Normal-butylamine N,N-Di-n-butylamine n-butyl-1-butanamin DIBUTYLAMINE DIBUTYLAMINE IN TOLUENE LABOTEST-BB LTBB000395 n,n-dibutylamine DibutylaMine puriss., >=99.0% (GC) Dibutylamine > Dibutylamine, puriss, 99% Dibutylamine AR Dibutylamine LR Di-N-Butylamine, for HPLC, Certified, Fisher Chemical Di-N-Butylamine, Pure, Fisher Chemical Dibuthylamine Dibutylamin DNBA DI-N-BUTYLAMINE N-BUTYL-1-BUTANAMINE N-DIBUTYLAMINE Dibutylamine standard solution Naproxen Impurity 43 Di-N-Butylamine 99% For Synthesis 111-92-2 111922 CD3CD232NH CH3CH2CH2CH22NH C4H92NH CH3CH232NH Organic Building Blocks Nitrogen Compounds AMINE