Lonwin Industry group limited as a professional manufactor & exporter of chemical materials ,we totally haver more than 270 stuffs, we have been on this line for more than 9 years. Our chemical materials are exported to lot of countries and reg
Cas:102-69-2
Min.Order:100 Kilogram
Negotiable
Type:Other
inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
Cas:102-69-2
Min.Order:1 Metric Ton
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Type:Manufacturers
inquiryProduct description: Product name Tripropylamine CAS number 102-69-2 Assay ≥99% Appearance Colorless transparent liquid Capacity 1000mt/year Application Pharmaceutical, pesti
Cas:102-69-2
Min.Order:100 Gram
FOB Price: $12.0
Type:Lab/Research institutions
inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
high quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
Tri-n-butylamine Structural formula: Molecular weight: 143.27 Density(g/ml, 20°C): 0.76 Boiling point (°C): 156 Refractive index (nD20): 1.4155-1.4175 Flash point (°C): 32.5 Sales Index: Item Name Index
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis
Cas:102-69-2
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
Our company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung, LG, Merck, Thermo Fisher Scientific and so o
Cas:102-69-2
Min.Order:1 Metric Ton
Negotiable
Type:Lab/Research institutions
inquiryCAS No.: 102-69-2 EINECS RN: 203-047-7 Molecular Formula: C9H21N Molecular Weight: 143.27 Use: Use:d for pharmacy, pesticide, rubber etc.
Cas:102-69-2
Min.Order:5 Metric Ton
FOB Price: $1.0 / 2.0
Type:Other
inquiryMinimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,MoneyGram Package 10g,20g,50g,100g,500g,1KGS,
Cas:102-69-2
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Cas:102-69-2
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
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
Superior quality Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used as a solvent. Transportation:as per your reques
Cas:102-69-2
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiry1)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 etc. 3) oem/odm available; 4) rea
Cas:102-69-2
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryProduct Name:Tri-n-propylamine CAS: 102-69-2 MF: C9H21N MW: 143.27 EINECS: 203-047-7 mp 93.5 °C(lit.) bp 155-158 °C(lit.) density 0.753 g/mL at 25 °C(lit.) vapor …
Best service,high quality and cheap price. Storage:Keep away from heat,sparks and flames. Package:25kg/50kg/200kg drum or Customer demand Application:Used as pharmaceutical intermediates Transportation:BY sea/air or by courier
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
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:102-69-2
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep 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
Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
bulk?production Application:Pharmaceutical intermediates
Cas:102-69-2
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiry1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:102-69-2
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryN,N-Dipropyl-1-propanamine Basic information Product Name: N,N-Dipropyl-1-propanamine Synonyms: (n-C3H7)3N;1-Propanamine,N,N-dipropyl-;n,n-dipro
Cas:102-69-2
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryService we provide: 1. before shipment, free sample for test 2. packing as your request, with oem brand name 3. top quality with best price 4. fast shipment by reputed shipping line 5. best service after shipment with emails Appearance:Colorle
Competitive price with superior quality; Factory; Technical support Appearance:colorless transparent liquid Storage:Store in dry,cool and ventilated place Package:150kg/drum Application:Organic synthesis intermediate Transportation:by express,
Known for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers.1) Standard:BP/USP/EP/Enterprise standard2) All Purity≥99%3) We are manufacturer and can provide high quality products with factory pric
Cas:102-69-2
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
di(rhodium)tetracarbonyl dichloride In ethanol at 115℃; under 37503 Torr; for 1.5h; | 100% |
propylamine
ethene
carbon monoxide
A
tri-n-propylamine
B
di-n-propylamine
Conditions | Yield |
---|---|
di(rhodium)tetracarbonyl dichloride In ethanol at 119℃; under 44253.5 Torr; for 1h; | A 1% B 99% |
di(rhodium)tetracarbonyl dichloride In ethanol at 119℃; under 44253.5 Torr; for 1h; | A 2% B 98% |
propan-1-ol
octanol
propiononitrile
A
tri-n-propylamine
B
Dipropyloctylamin
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 95% |
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 90% |
propiononitrile
A
tri-n-propylamine
B
N-propylidenepropylamine
C
di-n-propylamine
Conditions | Yield |
---|---|
With hydrogen at 220℃; | A 8.5% B 2.5% C 89% |
With hydrogen at 240℃; Temperature; Flow reactor; | A 13% B 2.5% C 80% |
propan-1-ol
1-Decanol
propiononitrile
A
tri-n-propylamine
B
N,N-dipropyldecylamine
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 86% |
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 80% |
propan-1-ol
1-dodecyl alcohol
propiononitrile
A
tri-n-propylamine
B
N,N-Dipropyl-dodecyl amine
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 80% |
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 76% |
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% |
propan-1-ol
1-Hexadecanol
propiononitrile
A
tri-n-propylamine
B
N,N-dipropylhexadecylamine
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A n/a B 75% |
1-Nitropropane
A
propan-1-ol
B
tri-n-propylamine
C
propiononitrile
Conditions | Yield |
---|---|
With carbon monoxide; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 12160 Torr; for 48h; Product distribution; other N-O compounds, effect of catalysts: Rh6(CO)16-amine polymers, -(CH3)2N(CH2)3N(CH3)2, (CH3)3N, (C3H7)3N; | A 19% B 4% C 72% |
With carbon monoxide; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 12160 Torr; for 48h; | A 19% B 4% C 72% |
With carbon monoxide; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 12160 Torr; for 48h; | A 32% B 3% C 55% |
With carbon monoxide; (CH3)2NC3H6NH-substituted polystyrene; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 12160 Torr; for 48h; Title compound not separated from byproducts; | A 19 % Chromat. B 3 % Chromat. C 72 % Chromat. |
Conditions | Yield |
---|---|
With hydrogen; Cu/Co/Ni/gamma-Al2O3 catalyst at 220℃; under 63756.4 Torr; Product distribution / selectivity; | A 4% B 49% |
1-Nitropropane
A
propan-1-ol
B
tri-n-propylamine
C
n-hexan-3-one
D
propiononitrile
Conditions | Yield |
---|---|
With carbon monoxide; water; hexarhodium hexadecacarbonyl; trimethylamine In 2-ethoxy-ethanol at 40℃; under 12160 Torr; for 24h; | A 16% B 8% C 7% D 40% |
With carbon monoxide; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 12160 Torr; for 48h; | A 7% B 4% C 18% D 31% |
With N,N,N'N'-tetramethyl-1,3-propanediamine; carbon monoxide; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 12160 Torr; for 24h; Product distribution; Mechanism; aminosubstituded polystyrenes or other amines instead of TMPDA, other solvents, recycling of polystyrene-bound Rh-cluster complex; | A 15 % Chromat. B 4 % Chromat. C 0 % Chromat. D 71 % Chromat. |
With carbon monoxide; amino-substituted polystyrene; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 12160 Torr; for 48h; Title compound not separated from byproducts; | A 7 % Chromat. B 4 % Chromat. C 18 % Chromat. D 31 % Chromat. |
Conditions | Yield |
---|---|
With phosphoric acid; ammonia at 250 - 500℃; |
Conditions | Yield |
---|---|
With ammonia; platinum under 2280 Torr; Hydrogenation; | |
With water; palladium under 2280 Torr; Hydrogenation; |
tetrapropylammonium
A
tri-n-propylamine
B
propene
Conditions | Yield |
---|---|
With water durch Destillation; |
tripropylamine oxide
tri-n-propylamine
Conditions | Yield |
---|---|
With sulfur dioxide; water | |
With N,N,N'N'-tetramethyl-1,3-propanediamine; carbon monoxide; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 6080 Torr; for 24h; | 91 % Chromat. |
With N,N,N'N'-tetramethyl-1,3-propanediamine; carbon monoxide; water; hexarhodium hexadecacarbonyl In 2-ethoxy-ethanol at 40℃; under 6080 Torr; for 24h; Product distribution; Mechanism; (CH3)2NC3H6NH-substituted polystyrene instead of TMPDA; analogous reaction of another amine oxide; | 91 % Chromat. |
tripropylamine oxide
A
tri-n-propylamine
B
propene
C
N,N-di-n-propylhydroxylamine
Conditions | Yield |
---|---|
beim Erhitzen unter gewoenlichem Druck; |
Conditions | Yield |
---|---|
With nickel at 162 - 195℃; under 36775.4 - 73550.8 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With ammonia; platinum under 2280 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With platinum under 2280 Torr; Hydrogenation; | |
With 5%-palladium/activated carbon; ammonium formate In hexane at 20℃; | |
With hydrogen at 70℃; under 750.075 Torr; for 6h; chemoselective reaction; |
tributyl-amine
tri(n-propyl)amine-H+
A
tri-n-propylamine
B
tributylammonium
Conditions | Yield |
---|---|
at 176.9℃; Rate constant; Thermodynamic data; Kinetics; var. temp.; ΔH0, ΔS0; |
propionaldehyde
A
propylamine
B
tri-n-propylamine
C
di-n-propylamine
Conditions | Yield |
---|---|
With ammonia; hydrogen; 20% Ni/Al2O3; nickel at 180℃; Product distribution; influence of nature of the catalyst and temperature; | A 49.7 mol B 2.8 mol C 44.3 mol |
1-phenylethyltripropylammonium bromide
A
styrene
B
tri-n-propylamine
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol at 60℃; Rate constant; Mechanism; |
1-phenylethyltripropylammonium-2,2,2-d3 bromide
A
tri-n-propylamine
B
styrene-d2
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol at 60℃; Rate constant; Mechanism; hydrogen-deuterium isotop effect; |
propylamine
A
tri-n-propylamine
B
isocapronitrile
C
N-propylidenepropylamine
D
di-n-propylamine
E
propiononitrile
Conditions | Yield |
---|---|
Cu-MFI/VIE In gas at 299.85℃; for 2h; Product distribution; other catalysts; var. reaction times; |
Conditions | Yield |
---|---|
at 25℃; unter 3 Atm. Wasserstoff-Ueberdruck.Hydrogenation; |
Conditions | Yield |
---|---|
at 25℃; under 2280 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
In acetonitrile for 24h; Reflux; | 100% |
In 1,2-dichloro-ethane at 30℃; for 6h; | 98% |
tri-n-propylamine
phosphoric acid
Conditions | Yield |
---|---|
In water High Pressure; hydrothermal synthesis; V2O5/H3PO4/amine/H2O=1:7:>10:1400, heating for 10 d at 200°C; washing (H2O), drying in air; | 99% |
tri-n-propylamine
1,3,5-trichloro-2,4,6-triazine
2,4,6-tris-(N,N-dipropylamino)-1,3,5-triazine
Conditions | Yield |
---|---|
In dichloromethane at 0℃; | 98% |
Conditions | Yield |
---|---|
With hydrogenchloride; [Cp*IrCl(C5H4CH2C5H3OH)][Cl] In methanol at 120℃; for 12h; Schlenk technique; | 96% |
tri-n-propylamine
2-chlorobenzo[d][1,3]thiazole
N,N-dipropylbenzo[d]thiazol-2-amine
Conditions | Yield |
---|---|
at 100℃; under 6000480 Torr; for 96h; | 95% |
Conditions | Yield |
---|---|
In acetonitrile at 25℃; for 24h; | 95% |
tri-n-propylamine
2-chloro-4,6-dimethoxy-1 ,3,5-triazine
2,4-dimethoxy-6-(di-n-propylamino)-1,3,5-triazine
Conditions | Yield |
---|---|
In toluene Reflux; | 95% |
Conditions | Yield |
---|---|
In ethanol Reflux; Inert atmosphere; | 95% |
In acetone for 24h; Reflux; |
Conditions | Yield |
---|---|
In ethanol Reflux; Inert atmosphere; | 95% |
2,3-dimethyl-6,7-dihydro-5H-2a-thia-(2a-SIV)-2,3,4a,7a-tetraazacyclopentindene-1,4(2H,3H)-dithione
tri-n-propylamine
3-Methyl-1,1-dipropyl-thiourea
Conditions | Yield |
---|---|
In benzene for 24h; Irradiation; | 94% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon In toluene at 175℃; for 1.5h; Inert atmosphere; Microwave irradiation; | 94% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon In toluene at 175℃; for 1.5h; Inert atmosphere; | 94% |
tri-n-propylamine
4-toluenesulfonyl azide
(E)-N'-((4-methylphenyl)sulfonyl)-N,N-dipropylformimidamide
Conditions | Yield |
---|---|
With tert-butylammonium hexafluorophosphate(V) In acetonitrile at 25℃; for 3h; Electrolysis; | 94% |
With 10-phenyl-9-(2,4,6-trimethylphenyl)acridinium tetrafluoroborate In 1,2-dichloro-ethane at 20℃; for 10h; Irradiation; | 85% |
With tert.-butylhydroperoxide In water; 1,2-dichloro-ethane at 80℃; for 8h; | 80% |
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; acetic acid In acetonitrile at 20℃; for 24h; Irradiation; Sealed tube; | 94% |
tri-n-propylamine
C5H5FeC5H3CH3CH2N(CH3)3(1+)*I(1-)=[C5H5FeC5H3CH3CH2N(CH3)3]I
C5H5FeC5H3CH3CH2N((CH2)2CH3)3(1+)*I(1-)=C5H5FeC5H3CH3CH2N((CH2)2CH3)3I
Conditions | Yield |
---|---|
In acetonitrile ferrocenyl deriv. refluxed with 3 equiv. of a tertiary amine for 17-18 hunder Ar; cooled., evapd., residue dissolved in acetone, diluted with a large amt.of Et2O and left to stand at -2-4°C; crystalline ppt. collected; | 93.6% |
tri-n-propylamine
iodobenzene
carbon monoxide
N,N-dipropylbenzamide
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; oxygen In acetonitrile at 100℃; under 4560.31 Torr; for 8h; Autoclave; Green chemistry; | 93% |
With palladium dichloride In water at 80℃; under 760.051 Torr; for 8h; Green chemistry; | 85% |
With iodophenylbis(triphenylphosphine)palladium at 120℃; for 67h; | 23.9% |
tri-n-propylamine
Conditions | Yield |
---|---|
With tetrafluoroboric acid In water at 0℃; for 0.5h; | 93% |
With tetrafluoroboric acid In water at 40 - 60℃; for 24h; | 87.2% |
With tetrafluoroboric acid In water at -0.16℃; | 36.5% |
Conditions | Yield |
---|---|
In water for 0.5h; Cooling with ice; | 93% |
In water for 0.5h; Cooling with ice; | 93% |
tri-n-propylamine
Conditions | Yield |
---|---|
With hydrogenchloride | 92% |
Conditions | Yield |
---|---|
With chlorotribromomethane; Eosin Y In dichloromethane; water at 20℃; for 3h; Irradiation; | 92% |
With antimony(III) chloride In 1,4-dioxane at 80℃; for 5h; | 74% |
With Eosin Y; water; oxygen In toluene at 20℃; for 20h; Schlenk technique; Irradiation; | 60% |
tri-n-propylamine
5,6-dihydro-6-ethyl-5-oxo-2-piperazinopyrido[4,3-d]pyrimidine
2-chloro-6,7-dimethoxy-quinazoline
Conditions | Yield |
---|---|
In i-Amyl alcohol | 92% |
Conditions | Yield |
---|---|
In water concd. HCl and N(C3H7)3 were added to a soln. of salt in water with stirring; the mixt. was extd. with CH2Cl2, dried over MgSO4, filtered, the solventwas removed under reduced pressure; | 92% |
Conditions | Yield |
---|---|
With [(phenylbenzothiazole)2Ir(nBu)3]OTf In 5,5-dimethyl-1,3-cyclohexadiene at 155℃; for 10h; Inert atmosphere; Schlenk technique; | 92% |
With μ-diiodo-di((η5-pentamethylcyclopentadienyl)(iodo)iridium) In 5,5-dimethyl-1,3-cyclohexadiene at 155℃; for 10h; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon In toluene at 175℃; for 1.5h; Inert atmosphere; Microwave irradiation; | 92% |
Conditions | Yield |
---|---|
With oxygen; acetic acid; copper(ll) bromide In 1,4-dioxane at 120℃; under 760.051 Torr; for 16h; | 92% |
Conditions | Yield |
---|---|
In ethanol Reflux; Inert atmosphere; | 92% |
tri-n-propylamine
Conditions | Yield |
---|---|
With hexafluorophosphoric acid In water for 0.25h; Cooling with ice; | 92% |
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