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HCID 8148Erstellt: 26. Oktober 2026

Di-n-butylamin

DI-N-BUTYLAMINE · DNBA · N-DIBUTYLAMINE · n,n-dibutylamine · Dibutylamin · Dibuthylamine · N-BUTYL-1-BUTANAMINE · ai3-52649

https://huagongshe.com/de/chemical/8148

Molekülstruktur von Di-n-butylamin

Identifikatoren & physikalische Daten

CAS No.111-92-2
SummenformelC8H19N
Durchschnittliche Molmasse129,24 g/mol
Monoisotopische Masse129,15174961 g/mol
SMILESCCCCNCCCC
InChIKeyJQVDAXLFBXTEQA-UHFFFAOYSA-N
PubChem CID8148
ChEMBLCHEMBL3184528
EC No.203-921-8
DTXSIDDTXSID7024952
Lokaler NameDi-n-butylamin

Chemische & physikalische Eigenschaften

XLogP2,8
Polarare Oberfläche (TPSA)12
H-Brücken-Donoren1
H-Brücken-Akzeptoren1
Frei drehbare Bindungen6
Schwere Atome9
Formalladung0
Komplexität37,8
StoffklassenNitrogen Compounds -> Amines, AliphaticCorrosives
SpringerMaterials Properties15N nuclear magnetic resonance spectrum
PestizideEnvironmental transformation -> Pesticide transformation products (metabolite, successor)
LogP (Verteilungskoeffizient)log Kow= 2.832.68
GeruchAMMONIA-LIKE ODOR
Dichte0.759 at 68 °F (USCG, 1999) - Less dense than waterwill float0.7601 @ 20 °C/4 °CDensity (at 20 °C): 0.76 g/cm³Relative density of the vapour/air-mixture at 20 °C (air = 1): 1.010.7613 @ 20°C0.767 g/mL at 25 °C(lit.)
Color/FormLiquidColorless
LöslichkeitSoluble (NTP, 1992)Sol in alcoholVery sol in ether and ethanolsol in acetone3500 mg/l in water @ 25 °CSolubility in water, g/100ml: 0.35 (slightly soluble)water: soluble3.8g/L at 20°C4.05 g/L (25 ºC)
Flammpunkt125 °F (NTP, 1992)57 °C57 °C (open cup)51.6 °C (open cup)47 °C106 °F
Siedepunkt318 to 320 °F at 760 mmHg (NTP, 1992)159-160 °C159 °C159.6 °C @760 [mm Hg]159 °C(lit.)
DecompositionWhen heated to decomp it emits toxic fumes of /nitrogen oxides/.Products of decomposition include carbon monoxide, carbon dioxide, hydrocarbons, & oxides of nitrogen as well as amine vapors.
Schmelzpunkt-76 to -74 °F (NTP, 1992)-60 to -59 °C-61.9 °C−62 °C(lit.)
Dampfdichte4.46 (vs air)
Dampfdruck1.9 mm Hg ( 20 °C)
Brechungsindexn20/D 1.417(lit.)
LagerbedingungenStore below +30°C.
pKa (Säurekonstante)11.25(at 21℃)
AggregatzustandLiquid
FarbeWhite
pH11.1 (1g/l, H2O, 20℃)
GeruchWeak ammonia.
Explosionsgrenze0.6-6.8%(V)
Spezifische WärmekapazitätCp(liquid): 2.27 J/(g·K), at 25℃
Merck14,3032
BRN506001
Henry-Konstante1.3×10-1 mol/(m3Pa) at 25℃, Brockbank (2013)
Dielektrizitätskonstante3.0(20℃)
StabilitätStable. 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.
InChI1S/C8H19N/c1-3-5-7-9-8-6-4-2/h9H,3-8H2,1-2H3
InChIKeyJQVDAXLFBXTEQA-UHFFFAOYSA-N
SMILESCCCCNCCCC
LogP (Verteilungskoeffizient)2.1 at 23℃
CAS Datenbank111-92-2(CAS DataBase Reference)
NIST chemische Informationen1-Butanamine, N-butyl-(111-92-2)
EPA chemische InformationenDibutylamine (111-92-2)

Sicherheit & Vorschriften

GHS-EinstufungDangerH226: Flammable liquid and vapor [Warning Flammable liquids]P210, P233, P240, P241, P242, P243, P260, P262, P264, P264+P265, P270, P271, P280, P284, P301+P316, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P320, P321, P330, P361+P364, P363, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]P210, P233, P240, P241, P242, P243, P260, P261, P262, P264, P264+P265, P270, P271, P280, P284, P301+P316, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P320, P321, P330, P361+P364, P362+P364, P363, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Regulatorische InformationenChemical: 1-Butanamine, N-butyl-1-Butanamine, N-butyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1-Butanamine, N-butyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)Status: Active Update: 01-07-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/135271-Butanamine, N-butyl-: Does not have an individual approval but may be used under an appropriate group standardThe New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)
DOT-KennzeichnungCorrosive Flammable Liquid
BrandgefahrenSpecial Hazards of Combustion Products: Toxic oxides of nitrogen may form in fires. (USCG, 1999)· Flammable/combustible material.Flammable. Gives off irritating or toxic fumes (or gases) in a fire. Above 47 °C explosive vapour/air mixtures may be formed. Risk of fire and explosion on contact with strong acids or strong oxidizing agents.
BrandpotenzialFLAMMABLE LIQUID WHEN EXPOSED TO HEAT OR FLAME ... .
GesundheitsgefahrenInhalation causes irritation of nose, throat, and lungscoughingnauseaheadache. Ingestion causes irritation of mouth and stomach. Contact with eyes causes irritation. Contact with skin causes irritation and dermatitis. (USCG, 1999)· May cause toxic effects if inhaled or ingested.
GefahrenübersichtCorrosive to skin[Quick CPC] Causes severe burns to the eyes and skinHigh inhalation exposure can cause pulmonary edema[HSDB] A corrosive substance that can cause pulmonary edema[ICSC]
DOT-Nummer und Handbuch2248 132
Reaktive GruppeAmines, Phosphines, and Pyridines
UN-EinstufungUN Hazard Class: 8UN Subsidiary Risks: 3UN Pack Group: II
TSCA-AnforderungenPursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. Dibutylamine is included on this list.
Reactivity ProfileDI-N-BUTYLAMINE 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.
Chemical DangersDecomposes on burning. This produces toxic fumes including nitrogen oxides. The substance is a strong base. Reacts violently with strong oxidants. This generates fire and explosion hazard. Attacks some metals and some plastics. Solutions in water slowly etch glass.
BrandbekämpfungExcerpt from ERG Guide 132 [Flammable Liquids - Corrosive]:Use alcohol-resistant foam, water, powder, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
Erste-Hilfe-MaßnahmenFresh air, rest. Half-upright position. Artificial respiration may be needed. Refer immediately for medical attention.Wear protective gloves when administering first aid. Remove contaminated clothes. Rinse skin with plenty of water or shower for at least 15 minutes. Refer immediately for medical attention .Rinse with plenty of water for several minutes (remove contact lenses if easily possible). Refer immediately for medical attention.Rinse mouth. Give nothing to drink. Do NOT induce vomiting. Refer immediately for medical attention.
Freisetungsmaßnahmen· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
Erste HilfeEYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.General First Aid:
Sichere LagerungFireproof. Store only in original container. Separated from strong oxidants, strong acids and food and feedstuffs. Store in an area without drain or sewer access. Provision to contain effluent from fire extinguishing.
Expositionsschutz und Persönliche Schutzausrüstung· Wear positive pressure self-contained breathing apparatus (SCBA).173.0 [ppm]
BrandbekämpfungsverfahrenUse water spray, dry chemical, foam, or carbon dioxide. Use water spray to keep fire-exposed containers cool.USE WATER SPRAY, DRY CHEM, "ALCOHOL" FOAM, OR CARBON DIOXIDE. USE WATER SPRAY TO KEEP FIRE-EXPOSED CONTAINERS COOL. IF LEAK OR SPILL HAS NOT IGNITED, USE WATER SPRAY TO DISPERSE VAPORS & TO PROTECT MEN ATTEMPTING TO STOP LEAK. WATER SPRAY MAY BE USED TO FLUSH SPILLS AWAY FROM EXPOSURES.
LagerbedingungenSeparate from oxidizing materials, acids, and sources of halogens. Store in a cool, dry, well-ventilated location. Outside or detached storage is peferred.
Freisetung ohne BrandExcerpt from ERG Guide 132 [Flammable Liquids - Corrosive]:
EntsorgungsverfahrenSRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
Verschüttetes entsorgenRemove all ignition sources. Personal protection: complete protective clothing including self-contained breathing apparatus. Do NOT let this chemical enter the environment. Cover the spilled material with inert absorbent or sand. Then store and dispose of according to local regulations. Wash away remainder with plenty of water.
Preventive MeasuresSRP: Local exhaust ventilation should be applied wherever there is an incidence of point source emissions or dispersion of regulated contaminants in the work area. Ventilation control of the contaminant as close to its point of generation is both the most economical and safest method to minimize personnel exposure to airborne contaminants.SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.
KörperbelastungDibutylamine was found in the expired air of 6.5% of a sample of 54 carefully selected normal, healthy, nonsmoking adults who resided in urban areas(1). The geometric mean concn level was 0.218 ng/l(1).
WechselwirkungenNitrite ... is used as a food additive in meats and smoked fish. Some fish, vegetables, and fruit juices contain secondary amines. The acidic environment of the stomach facilitates a chemical reaction between nitrite and secondary amines, leading to the formation of carcinogenic nitrosamines. /Secondary amines/
UmweltverhaltenTERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 825(SRC) for the unprotonated form from a log Kow of 2.83(2) and a regression derived equation(3) indicates that dibutylamine is expected to have low mobility in soil(SRC). A pKa value of 11.39(4) indicates that the protonated form of dibutylamine will be the dominant species in moist soil surfaces and cations generally adsorb strongly to soils. Volatilization of dibutylamine from moist soil surfaces is not expected to be an important fate process since the cation is not expected to volatilize. The potential for volatilization of dibutylamine from dry soil surfaces may exist(SRC) based upon a vapor pressure of 2.59 mm Hg at 25 °C(5). 94-97% of the theoretical BOD was achieved for dibutylamine using an activated sludge inoculum during a 4 week incubation period(6).AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 825(SRC) from a log Kow of 2.83(2) and a regression derived equation(3) indicates that dibutylamine is expected to adsorb to suspended solids and sediment in water(SRC). A pKa value of 11.39(4) indicates that the protonated form of dibutylamine will be the predominant species in water. Volatilization from water surfaces is not expected to be important fate process(SRC) since the protonated form will not volatilize at environmental pH. According to a classification scheme(5), an estimated BCF of 30(SRC), from its log Kow(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is moderate(SRC). In a screening study, dibutylamine completely degraded within 14 days at 10 ppm with both an activated sludge and freshwater sediment inoculum(7).ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), dibutylamine, which has a vapor pressure of 2.59 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase dibutylamine is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC)the half-life for this reaction in air is estimated to be 4 hours(SRC), from its rate constant of 8.98X10-11 cu cm/molecule-sec at 25 °C(3). Dibutylamine is not expected to directly photolyze due to the lack of absorption in the environmental UV spectrum(SRC).
Lebensmitteluntersuchungswerte... Amines from decomposing fish have been suspected as a cause of keratitis. ... /Amines/Dibutylamine was detected in pepperoni at a concn of 3.4 ppm(1). An average dibutylamine concn of 10 ppb was found in 3 samples of cod roehowever, it was not detected in samples of fish sausage, baked ham, spinach, or miso(2).
Unerwünschte WirkungenDermatotoxin - Skin burns.
ExpositionspfadeSerious local effects by all routes of exposure.
Signs and SymptomsCough. Sore throat. Burning sensation. Shortness of breath. Laboured breathing.Redness. Pain. Serious skin burns.Redness. Pain. Blurred vision. Severe burns.Burns in mouth and throat. Burning sensation behind the breastbone. Abdominal pain. Vomiting. Shock or collapse.
Effluent ConcentrationsIn a comprehensive survey of wastewater from 4000 industrial and publicly owned treatment works (POTWs) sponsored by the Effluent Guidelines Division of the U.S. EPA, dibutylamine was identified in discharges of the following industrial category (frequency of occurrence, median concn in ppb): iron and steel mfg (4170.4), plastics and synthetics (189.1), electronics (16723.3)(1). Dibutylamine was reported to be released from effluent of sewage treatment plants(2).
ICSC Environmental DataThe substance is toxic to aquatic organisms.
Soil Adsorption/MobilityThe Koc of dibutylamine was estimated as 825(SRC), using a log Kow of 2.83(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that dibutylamine is expected to have low mobility in soil(SRC). The pKa of dibutylamine is 11.73(4), indicating that the protonated form will be the predominant species in moist soils and cations are expected to adsorb strongly to soil surfaces.
TSCA Test SubmissionsAcute inhalation toxicity was evaluated in groups of 5 male and 5 female Sprague-Dawley albino rats exposed to dibutylamine at actual concentrations of 0.76, 1.08, 1.18, 1.39 or 3.91 mg/l of air for 4 hours. Mortality was observed in 2 animals in the 0.76 mg/l dose group, 4 in the 1.18 mg/l dose group, and all 10 in both the 1.39 and 3.91 mg/l dose groups. The LC50 value was calculated to be 1.15 mg/l (standard error of 0.095 mg/l) by the log probit method of Miller and Tainter. Clinical observations included excessive salivation, lacrimation, gasping, convulsions, abnormal breathing, ataxia, lethargy, rales, and staining of the urogenital area. Gross necropsy revealed lung congestion in decedents.The inhibition of nonspecific esterase activity, and/or inhibition of aromatic amino acid esterase activity, and/or potential effects on specific cellular functions (phagocytosis, immunoglobin G synthesis, and inflammatory and immune mediator release) were evaluated with organic chemicals added to human peripheral blood monocytes. Di-n-butylamine stimulated monocyte alpha- naphthyl acetate esterase activity by 104% at a concentration of 1 mM, and 116% at 0.25 mM and stimulated monocyte aromatic amino acid esterase activity by 103% at 250 uM. Only the low-dose value for alpha-naphthyl acetate esterase stimulation was considered to be statistically significant.The dermal sensitization potential of di-n-butylamine (CAS # 111-92-2) was evaluated in 10 CF1(BR) mice inducted with 3 daily 0.1 ml topical applications of a 0.1% (v/v in ethanol) test solution to clipped abdomens. A group of 10 mice likewise inducted over 3 days with 0.1 ml dermal applications of 0.5% (w/v) DNCB served as the positive control. Challenge and rechallenge were administered 7 and 14 days later in .01 ml dermal applications of a 25% (v/v) solution to both dorsal and ventral surfaces of the left and right ears respectively of inducted test mice. The thickness of treated left ears relative to that of solvent control (ethanol) right ears indicated the degree of sensitization. One animal challenged with di-n-butylamine exhibited a positive sensitization response (20% increase in ear thickness over control) at 48-hour evaluation only. None of either test or irritation control groups had responded to challenge by the 24-hour evaluation and none responded to rechallenge. Conversely, 60% and 50% positive response in the DCNB-inducted and challenged groups at 24-hour and 48-hour evaluations, respectively, confirmed the validity of the test system.The clastogenic potential of di-n-butylamine (CAS # 111-92-2) was evaluated by incidence of micronucleated polychromatic erythrocytes in bone marrow of Harlan Sprague-Dawley ICR mice (20/sex/group) administered single oral gavage doses at 55, 110, or 220 mg/kg bodyweight. Mortality occurred among high-dose males (3/20) and females (1/20), and lethargy was observed in both males and females of all treatment groups. While treated mice exhibited slight reductions in polychromatic erythrocytes to erythrocyte ratios (up to 19%) relative to vehicle control (corn oil) animals, there was no significant increase in micronucleated polychromatic erythrocytes at 24, 48 or 72-hour post-treatment examination in either male or female treated mice when compared to controls.
Natural Pollution SourcesThere is some indication that dibutylamine may occur naturally in some soils(1) and food items(2). Amines are produced by microbial processes in decaying organic matter and dibutylamine's emission from sewage treatment plants(3) suggests that it may also be a product of microbial metabolism(SRC).
F10
Wassergefährdungsklasse (WGK)1
TSCA-Inventar-StatusTSCA listed
UN-TransportnummerUN 2248
Zollcode2921 19 99
RTECS-Nr.HR7780000
R-Sätze (R)10-20/21/22-35-23-21/22
ToxizitätLD50 orally in rats: 550 mg/kg (Smyth)
GefahrensymboleXn,T
Sicherheitshinweise (S)45-36/37/39-28A-26-23
Gefahrenklasse8Acute Tox. 2 InhalationAcute Tox. 3 DermalAcute Tox. 4 OralEye Dam. 1Flam. Liq. 3Skin Corr. 1A
VerpackungsgruppeII
Lagerklasse3 - Flammable liquids
Gefahrstoffdaten111-92-2(Hazardous Substances Data)
Selbstentzündungstemperatur594 °F

Anwendungen & Verwendung

Verwenden

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.