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inquiryTributylamine CAS 102-82-9 N,N-Dibutyl-1-butanamine CAS no 102-82-9 1-Butanamine,N,N-dibutyl- Tributylamine N,N-Dibutyl-1-butanamine 1-Butanamine,N,N-dibutyl- Tributylamine CAS 102-82-9 IN Stock N,N-Dibutyl-1-butanamineCAS 102-82-9 Tribu
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inquiryCAS code: 102-82-9 Chemical name: Tri-n-butylamine Molecular formula: C12H27N Molecular weight: 185.35
WITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturing
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inquiry1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ
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inquiryTributylamine CAS: 102-82-9 Specification Item Standard Identification A.H-NMR:Comply with the structure B.LC-MS:Comply with the structure C.The IR spectrum of sa
Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquirySuperior quality Appearance:pale yellow liquid with an amine odour Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bottle,25kg/drum or as per your request Application:Used as an inhibitor in hydraulic fluids.
Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Product Name: Tributylamine Synonyms: TBA;N,N-DIBUTYL-1-BUTANAMINE;TRIBUTYLAMINE;TNBA;TRI-N-BUTYLAMINE;(n-C4H9)3N;1-Butanamine, N,N-dibutyl-;1-Butanamine,N,N-dibutyl- CAS: 102-82-9 MF: C12H27N MW: 185.35 EINECS: 203-058-7 Product Categories:
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inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
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inquiryMy Company Changchun Artel Import and Export trade companyImport and Export Trade Co., Ltd.is located in Changchun, a national historical and cultural city, Jilin Province, China. It covers an area of 22,000 square meters, construction area
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Product Name:Tri-n-butylamine CAS: 102-82-9 MF: C12H27N MW: 185.35 EINECS: 203-058-7 mp 70 °C(lit.) bp 216 °C(lit.) density 0.778 g/mL at 25 °C(lit.) vapor density 6.38…
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou
1,we produce and sell good chemicals around the world.2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%.3,our staff consists of highly qualified in
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiryQuick Details CAS No.: 102-82-9 Other Names: N,N-Dibutyl-1-butanamine MF: C12H27N EINECS No.: 203-058-7 Place of Origin: China (Mainland) Type: Syntheses Mat
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inquiryexcellent quality and reliable supplierAppearance:COA mentioned Storage:COA mentioned Package:Standard or custom package Application:pharmaceutical raw materails Transportation:sea/air /courier Port:China main port
We product this chemical more than 130 years . We are very experience to export it to many countries, Our superior & stable quality , competitive price gain warm reception from our customers.Appearance:off white powder Application:intermediate
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
Seeking Development with Quality and Promoting with ReputationOccupy the market with services and compete for benefits with efficiencyTaizhou Longyu Chemical Co., Ltd. is a modern private enterprise that integrates research and development, productio
Conditions | Yield |
---|---|
With polymethylhydrosiloxane; bis(1,5-cyclooctadiene)diiridium(I) dichloride In tetrahydrofuran at 50℃; for 5h; | 99% |
With NiO doped titania In butan-1-ol Reagent/catalyst; Irradiation; | 93% |
With hydrogen; nickel at 120 - 140℃; |
Conditions | Yield |
---|---|
With C42H44ClN4P2Ru(1+)*Cl(1-); potassium tert-butylate; ammonium formate at 100℃; for 72h; | 95% |
With 1-hydroxytetraphenylcyclopentadienyl(tetraphenyl-2,4-cyclopentadien-1-one)-μ-hydrotetracarbonyldiruthenium(II); ammonium chloride; potassium hydroxide at 140℃; for 39h; Sealed tube; Inert atmosphere; | 99 %Chromat. |
Conditions | Yield |
---|---|
With BER-CuSO4 In methanol for 3h; Ambient temperature; | 93% |
With Dimethylphenylsilane In tetrahydrofuran at 20℃; for 24h; Inert atmosphere; | 88% |
With bis(tri-n-butyltin) In tetrahydrofuran at 50℃; for 1h; | 84% |
With BER-CuSO4 In methanol for 3h; Ambient temperature; other tertiary amine N-oxides and aromatic N-oxides, var. temp. and time; |
propyl cyanide
octanol
butan-1-ol
A
tributyl-amine
B
octyldibutylamine
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 92% |
Conditions | Yield |
---|---|
With 5-methyl-1,3,4-thiadiazol-2-amine; potassium hydroxide In ethanol; water at 25℃; for 1h; | 85% |
With sodium hydroxide; urea at 120℃; under 3102.97 Torr; for 40h; | 76.5% |
With ammonia |
Conditions | Yield |
---|---|
palladium at 160℃; for 5h; | A 8% B 85% |
propyl cyanide
butan-1-ol
nonyl alcohol
A
tributyl-amine
B
1-Dibutylamino-nonan
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 85% |
Conditions | Yield |
---|---|
With hydrogen at 200℃; | A 13% B 2% C 85% |
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 84% |
Conditions | Yield |
---|---|
With chlorohydridocarbonylbis(tricyclohexylphosphine)ruthenium(II) In toluene at 120℃; for 24h; Catalytic behavior; Reagent/catalyst; Schlenk technique; Inert atmosphere; | 82% |
With aluminium trichloride | |
With palladium/alumina at 199.84℃; under 760.051 Torr; Kinetics; |
Conditions | Yield |
---|---|
With ruthenium trichloride; triphenylphosphine In tetrahydrofuran at 185℃; for 8h; | 81% |
N-butylamine
A
tributyl-amine
B
N-butylidenebutylamine
C
dibutylamine
Conditions | Yield |
---|---|
With sodium nitroprusside at 20℃; N-alkylation; | A 3% B 8% C 81% |
Rh on carbon In water for 1h; microwave irradiation; | A 9 % Chromat. B 57 % Chromat. C 34 % Chromat. |
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 80% |
Conditions | Yield |
---|---|
With tetrabutylammonium tetrafluoroborate In acetone at 320℃; Product distribution; in a gas chromatograph; other temperature; various concentration of reagent; | A 77% B n/a |
propyl cyanide
1-dodecyl alcohol
butan-1-ol
A
tributyl-amine
B
di-n-butyl-dodecylamine
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 76% |
n-propylmagnesium bromide
tris(benzotriazol-1-ylmethyl)amine
tributyl-amine
Conditions | Yield |
---|---|
In tetrahydrofuran 1.) room temperature, 1 h, 2.) reflux, 5 h; | 75% |
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 75% |
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 75% |
propyl cyanide
1-Hexadecanol
butan-1-ol
A
tributyl-amine
B
Di-n-butyl-hexadecylamin
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 75% |
propyl cyanide
1-Tetradecanol
butan-1-ol
A
tributyl-amine
B
dibutyl-tetradecyl-amine
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 70% |
1,4-dibromobicyclo<2.2.1>heptane
A
tributyl-amine
B
norbornene
C
1-bromonorbornane
D
bis(1-norbornyl)mercury
Conditions | Yield |
---|---|
With tetra-n-butylammonium perchlorate In N,N-dimethyl-formamide Electrolysis; at 25°C, at mercury cathode, at -1.9 V; | A 24% B 68% C 4% D 3% |
With tetra-n-butylammonium perchlorate In N,N-dimethyl-formamide Electrolysis; at 25°C, at mercury cathode, at -1.8 V; | A 25% B 52% C 5% D 16% |
With tetra-n-butylammonium perchlorate In N,N-dimethyl-formamide Electrolysis; at 25°C, at mercury cathode, at -1.7 V; | A 20% B 45% C 4% D 17% |
With tetra-n-butylammonium perchlorate In N,N-dimethyl-formamide Electrolysis; at 25°C, at mercury cathode, at -1.6 V; | A 10% B 33% C 2% D 27% |
cis-dichlorobis(triethylphosphine)platinum(II)
tetrabutylammonium perchlorate
A
1-butylene
trans-chlorohydridobis(triethylphosphine)platinum(II)
C
tributyl-amine
Conditions | Yield |
---|---|
In acetonitrile; benzene Electrolysis; preelectrolyzing solvents/TBAP (activated alumina in soln.), adding cis-(PtCl2(PEt3)2), electrolyzing at -2.1 V to near zero current (Ar, 3h); filtering, evapg., reduction to dryness, adding charcoal, extg. (benzene), filtering, concg., chromy. (alumina, benzene/hexane), evapg.; gas chromy., elem. anal.; | A n/a B 63.3% C n/a |
In acetonitrile; benzene Electrolysis; preelectrolyzing solvents/TBAP, adding cis-(PtCl2(PEt3)2), electrolyzing at -2.1 V to near zero current (Ar, 3h); same products when benzonitrile (5 - 10 equiv.) was added; filtering, evapg., reduction to dryness, adding charcoal, extg. (benzene), filtering, concg., chromy. (alumina, benzene/hexane), evapg.; gas chromy., elem. anal.; |
propyl cyanide
A
tributyl-amine
B
butyl-1-idenedi-n-butylamine
C
dibutylamine
Conditions | Yield |
---|---|
With hydrogen at 260℃; Flow reactor; | A 13% B 23% C 61.5% |
ethylamine
N-butylamine
A
tributyl-amine
B
N-ethylbutylamine
C
N,N-diethylbutylamine
D
di-n-butylethylamine
E
dibutylamine
F
diethylamine
G
triethylamine
Conditions | Yield |
---|---|
With hydrogen at 200℃; under 6000.6 Torr; Reagent/catalyst; Temperature; | A n/a B 60.7% C n/a D n/a E n/a F n/a G n/a |
1,4-diiodobicyclo<2.2.1>heptane
A
tributyl-amine
B
norbornene
C
1,1'-binorbornane
D
bis(1-norbornyl)mercury
Conditions | Yield |
---|---|
With tetra-n-butylammonium perchlorate In N,N-dimethyl-formamide Electrolysis; at 25°C, at mercury cathode, at -1.9 V; | A 31% B 60% C 1% D 12% |
With tetra-n-butylammonium perchlorate In N,N-dimethyl-formamide Electrolysis; at 25°C, at mercury cathode, at -1.8 V; | A 23% B 46% C 1% D 27% |
Conditions | Yield |
---|---|
With {[(PCy3)(CO)RuH]4(μ-O)(μ-OH)2}; 4-tert-Butylcatechol In chlorobenzene at 130℃; for 16h; Glovebox; Schlenk technique; Sealed tube; chemoselective reaction; | A n/a B 46% |
With bis(triphenylphosphine)platinum(II) dichloride; tin(ll) chloride In benzene at 180℃; for 5h; stainless steel reactor, var. reag.: PtCl2(PhCN)2; | A 8 % Chromat. B 74 % Chromat. |
With tris(triphenylphosphine)ruthenium(II) chloride In methanol at 180℃; for 7h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
n-Octylamine
N-butylamine
A
tributyl-amine
B
N-n-butyl-N-n-octylamine
C
n-dioctylamine
Conditions | Yield |
---|---|
With platinum-nickel nanoclusters on activated carbon; hydrogen at 190℃; under 760.051 Torr; Flow reactor; chemoselective reaction; | A 14.5% B 28% C 40.3% |
trans-chlorohydridobis(triethylphosphine)platinum(II)
tetrabutylammonium perchlorate
A
1-butylene
trans-{PtH(CH2CN)(PEt3)2}
C
tributyl-amine
D
platinum
Conditions | Yield |
---|---|
In acetonitrile; benzene byproducts: H2; Electrolysis; electrochemically reducing trans-(PtH(Cl)(PEt3)2) at -2.1 V vs Ag/AgCl in CH3CN/C6H6 (5/2, v/v), terminating electrolysis at constancy of current; 36% of hydrido complex recovered; 31P NMR; | A n/a B 38% C n/a D n/a |
Conditions | Yield |
---|---|
at 120℃; for 6h; | 100% |
In toluene at 70℃; for 24h; | 92% |
at 70 - 80℃; | 78% |
tributyl-amine
tetramethyl (dichloromethylene)bisphosphonate
Conditions | Yield |
---|---|
In acetonitrile at 50℃; for 4h; | 100% |
tributyl-amine
tetramethyl (dibromomethylene)bisphosphonate
Conditions | Yield |
---|---|
In acetonitrile at 50℃; for 6h; | 100% |
tributyl-amine
P,P-Bis(1-methylethyl) P',P'-dimethyl (dichloromethylene)bisphosphonate
Conditions | Yield |
---|---|
In acetonitrile at 60℃; for 4h; | 100% |
Conditions | Yield |
---|---|
In acetonitrile for 72h; Reflux; | 100% |
In 1,2-dichloro-ethane at 40℃; for 6h; | 98% |
With meta-dinitrobenzene In acetonitrile at 75℃; for 7h; | 90% |
Conditions | Yield |
---|---|
With hydrogenchloride In diethyl ether at 0℃; for 0.5h; | 100% |
With hydrogenchloride In water at 135℃; | |
With hydrogenchloride In water at 20℃; for 0.333333h; | |
With chloro-trimethyl-silane In tetrahydrofuran; methanol for 0.5h; Inert atmosphere; Schlenk technique; |
3(5)-amino-1,2,4-triazole
diethyl (2,4,6-trifluoro-phenyl)-malonate
tributyl-amine
Conditions | Yield |
---|---|
Stage #1: 3(5)-amino-1,2,4-triazole; diethyl (2,4,6-trifluoro-phenyl)-malonate; tributyl-amine at 150℃; for 2h; Stage #2: With sodium hydroxide In water; toluene at 20 - 30℃; for 1.25h; | 100% |
2-deoxy-2-fluoro-6-L-glycero-β-1-phosphoryl-D-heptoglucopyranose
tributyl-amine
Conditions | Yield |
---|---|
In ethanol Product distribution / selectivity; | 100% |
Conditions | Yield |
---|---|
In acetonitrile for 48h; Inert atmosphere; Reflux; | 100% |
tributyl-amine
Conditions | Yield |
---|---|
With palladium on carbon; hydrogen In methanol; ethyl acetate at 20℃; under 1125.11 Torr; for 24h; | 100% |
2-deoxy-1-O-dibenzylphosphoryl-2-fluoro-3,4,6,7-tetra-O-pivaloyl-L-glycero-β-D-gluco-heptopyranose
tributyl-amine
Conditions | Yield |
---|---|
Stage #1: 2-deoxy-1-O-dibenzylphosphoryl-2-fluoro-3,4,6,7-tetra-O-pivaloyl-L-glycero-β-D-gluco-heptopyranose With palladium 10% on activated carbon; hydrogen; triethylamine In ethanol; ethyl acetate under 750.075 Torr; for 12h; Stage #2: With tetra(n-butyl)ammonium hydroxide In water at 20℃; for 26h; Inert atmosphere; Stage #3: tributyl-amine Further stages; | 100% |
tributyl-amine
2-(trimethylsilyl)phenyl trifluoromethanesulfonate
Conditions | Yield |
---|---|
With cesium fluoride In acetonitrile at 20℃; for 16h; | 100% |
Conditions | Yield |
---|---|
In methanol at 20℃; for 12h; | 100% |
Conditions | Yield |
---|---|
In ethanol at 82℃; for 24h; | 100% |
Conditions | Yield |
---|---|
NiO nanoparticles at 100℃; for 10h; | 99% |
at 25℃; under 7500600 Torr; for 18h; | |
at 20.05℃; Kinetics; |
Conditions | Yield |
---|---|
In acetonitrile for 48h; Inert atmosphere; Reflux; | 99% |
Conditions | Yield |
---|---|
In acetonitrile at 40℃; for 68h; | 99% |
In dichloromethane at 20℃; for 48h; | 85% |
In acetonitrile at 50℃; for 48h; | 82% |
In acetonitrile at 40℃; for 24h; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
In acetonitrile at 82℃; for 33h; Solvent; Temperature; Menshutkin Reaction; | 98.9% |
In acetonitrile for 24h; Heating; | 80% |
With ethanol |
Conditions | Yield |
---|---|
With manganese(III) oxide; oxygen In tetrahydrofuran at 140℃; under 3000.3 Torr; for 24h; Reagent/catalyst; Pressure; Solvent; Temperature; Autoclave; Green chemistry; | 98% |
With pyridine; copper(l) chloride In acetonitrile at 100℃; under 7500.75 - 22502.3 Torr; for 24h; Catalytic behavior; Pressure; Reagent/catalyst; Temperature; Autoclave; | 70% |
With Eosin Y In ethanol for 10h; Irradiation; | 36% |
With manganese(IV) oxide In benzene | |
With copper(I) oxide; oxygen In ethanol; N,N-dimethyl-formamide at 120℃; under 4500.45 Torr; for 8h; Autoclave; | 93 %Spectr. |
tributyl-amine
[Bis-(diisopropoxy-phosphoryl)-methyl]-phosphonic acid diethyl ester
Conditions | Yield |
---|---|
Stage #1: [Bis-(diisopropoxy-phosphoryl)-methyl]-phosphonic acid diethyl ester With trimethylsilyl bromide In dichloromethane silylation; Heating; Stage #2: tributyl-amine deesterification; | 98% |
tributyl-amine
Conditions | Yield |
---|---|
With cross-linked polyvinylpyrrolidone*N2O4; dinitrogen tetraoxide In dichloromethane for 3h; Heating; | 98% |
Conditions | Yield |
---|---|
With dichloro bis(acetonitrile) palladium(II); tetrabutylammomium bromide; 18O-labeled water; zinc(II) oxide In dimethyl sulfoxide at 100℃; for 16h; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran; acetonitrile for 48h; Reflux; | 98% |
In chloroform; acetonitrile for 96h; Reflux; Inert atmosphere; Schlenk technique; | 95% |
tributyl-amine
trifluorormethanesulfonic acid
tributylammonium triflate salt
Conditions | Yield |
---|---|
In dichloromethane at 0℃; for 0.0833333h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran; acetonitrile for 48h; Reflux; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran; acetonitrile for 48h; Reflux; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran; acetonitrile for 48h; Reflux; | 98% |
tributyl-amine
5,10,15,20-tetrakis[3-(4-bromobutoxy)phenyl]porphyrin magnesium(II)
Conditions | Yield |
---|---|
In chloroform; acetonitrile at 70℃; for 90h; Inert atmosphere; Darkness; | 97% |
Conditions | Yield |
---|---|
In chloroform; acetonitrile Reflux; Inert atmosphere; Schlenk technique; | 97% |
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