Hangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting 1,3-Diaminopropane 99% CAS:109-76-2 , Please contact us by email freely. We are leading exporter in China. If you really need this
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inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:109-76-2
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inquiryDayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:109-76-2
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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
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inquiryhe company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality se T rvice Appearance:White or
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
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Cas:109-76-2
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inquiryOur 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
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inquiry1,3-Propanediamine CAS No.: 109-76-2 Molecular:C3H10N2 Molecular weight:74.13 Purity: 99.0% min. Properties : Colourless liquid. Melting point -12°C, boiling point 140°C, flash point @ 48°C, relative density @ 0.888, Refractiv
Hangzhou 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
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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
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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inquiryMassive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
Cas:109-76-2
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inquiryZibo 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
Cas:109-76-2
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inquiryOffer 1,3-Diaminopropane CAS:109-76-2 C3H10N2Appearance:white crystalline powder Storage:2-8, cold storage, to avoid light storage. Package:according to customers' requirements Application:109-76-2 1>Pharmaceutical raw materials and 2>pharmaceutic
Cas:109-76-2
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inquirySuperior quality, moderate price & quick delivery. 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:Is used in med
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 etc. 3) oem/odm available; 4) rea
Cas:109-76-2
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inquiry★.Best quality according to requirement ★.Competitive price in China market ★.Mature Technical support ★.Professional logistic support ★.Shortest delivery time . Appearance:Colorless liquid. Storage:Store in dry, cool and ventilated place Packag
Cas:109-76-2
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inquiryhigh 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
R & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
Cas:109-76-2
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inquirystable supply&competitive price Storage:Available Package:25KG Or as client requirement Application:Important pharm intermediate 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
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:109-76-2
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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
Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an
Cas:109-76-2
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inquiryOffer 1,3-Diaminopropane CAS:109-76-2 C3H10N2Appearance:white crystalline powder Storage:2-8, cold storage, to avoid light storage. Package:1g;5g;10g;25g;50g;100g;500g;1KG;5KG,25kg,50kg or as customers request Application:109-76-2 1>Pharmaceutical r
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inquiryConditions | Yield |
---|---|
95% | |
With ammonia; chlorocarbonylhydrido[4,5-bis(dicyclohexylphosphinomethyl)acridine]ruthenium(II) In toluene at 135℃; under 26402.6 Torr; for 12h; Autoclave; Inert atmosphere; | |
With chlorocarbonylhydrido[4,5-bis(dicyclohexylphosphinomethyl)acridine]ruthenium(II); ammonia In toluene at 135℃; under 26402.6 Torr; for 12h; Autoclave; Inert atmosphere; |
Trimethylenediamine
Conditions | Yield |
---|---|
With hydrogen; acetic acid In methanol | 89% |
2,2-dimethyl-1,1-bis(2-cyanoethyl)hydrazine
A
N1-(cyanoethyl)-1,3-propanediamine
B
1,1-dimethyl-2-(3-aminopropyl)hydrazine
C
Trimethylenediamine
D
2,2-dimethyl-1,1-bis(3-aminopropyl)hydrazine
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol Catalytic hydrogenation; Further byproducts given; | A n/a B n/a C n/a D 66.2% |
A
1,2-di-(3-pyridyl)-ethane
B
3-Methylpyridine
C
chromium(III) hexahydrate cation
D
Trimethylenediamine
Conditions | Yield |
---|---|
In perchloric acid Kinetics; (N2); decompn. of Cr complex in 1 M HClO4 depending on temp. under anaerobic conditions; not isolated, monitored by UV; | A 20% B 65% C n/a D n/a |
In perchloric acid Kinetics; decompn. of Cr complex in 1 M HClO4 depending on temp. under aerobic conditions; not isolated, monitored by UV; | A 38% B 11% C n/a D n/a |
Conditions | Yield |
---|---|
With chloroform; tris-(2-chloro-ethyl)-amine; sulfuric acid at 45℃; |
Conditions | Yield |
---|---|
With sodium-potassium alloy; butan-1-ol | |
With ammonia; hydrogen; nickel at 90℃; under 88260.9 Torr; |
3-azidopropylamine
Trimethylenediamine
Conditions | Yield |
---|---|
With hydrogenchloride im CO2-Strom; | |
With hydrogenchloride; tin(ll) chloride |
Conditions | Yield |
---|---|
With potassium hypobromite at 0 - 60℃; |
butanediol bis-(propionitrile)ether
Trimethylenediamine
Conditions | Yield |
---|---|
With ammonia; water; nickel at 100℃; Hydrogenation.unter Druck; |
pentanedioyl azide
Trimethylenediamine
Conditions | Yield |
---|---|
With hydrogenchloride; ethanol at 100 - 110℃; |
Conditions | Yield |
---|---|
With ethanol; ammonia; water |
Conditions | Yield |
---|---|
With ethanol; ammonia anschl. mit wss. NaOH, dann mit HCl, anschl. mit KOH; | |
With ethanol; ammonia at 100℃; im Autoklaven; |
Conditions | Yield |
---|---|
With sodium hydroxide; water; nitric acid at 150℃; under 51485.6 - 73550.8 Torr; Hydrogenation.an Raney-Nickel, anschl. Erwaermen mit NaOH; |
Conditions | Yield |
---|---|
With ammonia; nickel Hydrogenation.unter Druck; | |
With methanol; ammonia; water; hydrogen; nickel at 125℃; under 41188.4 - 61782.7 Torr; | |
With methanol; ammonia; water; hydrogen; nickel at 125℃; under 41188.4 - 61782.7 Torr; |
Conditions | Yield |
---|---|
With ammonia at 120℃; Rate constant; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.);; | |
With ammonium hydroxide; perchloric acid at 25℃; Rate constant; Thermodynamic data; E(a), ΔS(excit.); |
3-chloropropan-1-amine
Trimethylenediamine
Conditions | Yield |
---|---|
With ammonium hydroxide at 50℃; Rate constant; Thermodynamic data; E(a); |
Conditions | Yield |
---|---|
With pyrroloquinoline quinone In water at 37℃; examination of PQQ oxidation effect; phosphate buffer (pH=7.2); |
Conditions | Yield |
---|---|
With sodium hypochlorite; dimethylborane; ammonia 1.) 0 deg C, 1 h, 2.) O deg C; Yield given. Multistep reaction; |
(3-aminopropyl)carbamic acid benzyl ester hydrochloride
Trimethylenediamine
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol for 4h; Yield given; |
N-[1-(4-Hexadecyloxy-phenyl)-meth-(E)-ylidene]-N'-[1-(4-hexadecyloxy-phenyl)-meth-(Z)-ylidene]-propane-1,3-diamine
A
p-n-hexadecyloxybenzaldehyde
B
Trimethylenediamine
Conditions | Yield |
---|---|
With hydrogenchloride; water; cetyltrimethylammonim bromide In chloroform at 25℃; Rate constant; |
N-(3-aminopropyl)-1,4-diaminobutane
A
propionaldehyde
B
Trimethylenediamine
C
1,4-diaminobutane
Conditions | Yield |
---|---|
With NaPi buffer; oxygen at 37℃; for 0.166667h; catalase and polyamine oxidase presence, pH 6.5, other polyamines and acetylpolyamines, kinetic constants Km (μM) and Vmax (μmol H2O2 formed μg protein-1 min-1); |
Spermine
A
N-(3-aminopropyl)-1,4-diaminobutane
B
propionaldehyde
C
Trimethylenediamine
Conditions | Yield |
---|---|
With NaPi buffer; oxygen at 37℃; for 0.166667h; catalase and polyamine oxidase presence, pH 6.5, other polyamines and acetylpolyamines, kinetic constants Km (μM) and Vmax (μmol H2O2 formed μg protein-1 min-1); |
Conditions | Yield |
---|---|
With NaPi buffer; oxygen at 37℃; for 0.166667h; catalase and polyamine oxidase presence, pH 6.5, other polyamines and acetylpolyamines, kinetic constants Km (μM) and Vmax (μmol H2O2 formed μg protein-1 min-1); |
N1-Acetyl-Spermidine
Trimethylenediamine
Conditions | Yield |
---|---|
With NaPi buffer; oxygen at 37℃; for 0.166667h; catalase and polyamine oxidase presence, pH 6.5, other polyamines and acetylpolyamines, kinetic constants Km (μM) and Vmax (μmol H2O2 formed μg protein-1 min-1); |
Conditions | Yield |
---|---|
With KPi buffer; oxygen at 37℃; for 0.166667h; catalase and polyamine oxidase presence, both bound or not bound to hydroxyapatite, other reagent: NaPi buffer, pH 6 or 6.5, other polyamines and acetylpolyamines, kinetic constants Km (μM) and Vmax (μmol H2O2 formed μg protein-1 min-1); |
Conditions | Yield |
---|---|
With ammonia; hydrogen; Co-Fe catalyst at 195℃; under 37503 - 112509 Torr; Product distribution; | |
With ammonia; hydrogen; cobalt; iron at 195℃; under 101258 Torr; amination; | |
With ammonia; hydrogen; Co-La at 190℃; under 101258 Torr; amination; |
trimethyleneglycol
A
bis(3-aminopropyl)amine
B
propan-1-ol
C
Trimethylenediamine
D
propan-1-ol-3-amine
Conditions | Yield |
---|---|
With ammonia; hydrogen; carbon monoxide at 210℃; under 101258 Torr; Product distribution; Further Variations:; Catalysts; Temperatures; Pressures; amination; |
A
3-(2,5-dihydro-pyrrol-1-yl)-propylamine
B
Trimethylenediamine
Conditions | Yield |
---|---|
With sodium hydroxide; air; copper |
Trimethylenediamine
p-toluenesulfonyl chloride
N,N'-ditoluenesulfonyl-1,3-diaminopropane
Conditions | Yield |
---|---|
With potassium carbonate In tetrahydrofuran; water at 0.2℃; for 3h; Inert atmosphere; | 100% |
at 80℃; for 0.5h; | 95% |
With potassium carbonate In tetrahydrofuran; water at 23℃; for 10h; | 95% |
5-(dimethylamino)naphth-1-ylsulfonyl chloride
Trimethylenediamine
N-(3-aminopropyl)-5-(dimethylamino)naphthalene-1-sulfonamide
Conditions | Yield |
---|---|
In dichloromethane at 0℃; for 4h; | 100% |
In dichloromethane at 20℃; for 18h; Inert atmosphere; | 99% |
In dichloromethane at 0 - 20℃; for 1h; | 88% |
Trimethylenediamine
acrylonitrile
N1,N3-bis(2-cyanoethyl)propane-1,3-diamine
Conditions | Yield |
---|---|
In methanol at 20℃; for 16h; Addition; cyanoethylation; | 100% |
at 0℃; for 24h; Darkness; | 95% |
In ethanol at 20℃; for 16h; Addition; cyanoethylation; | 88% |
Trimethylenediamine
1-phenylbutan-1,3-dione
(Z)-3-{3-[(Z)-1-methyl-3-oxo-3-phenyl-1-propenylamino]propylamino}-1-phenyl-2-buten-1-one
Conditions | Yield |
---|---|
With silica-supported ferric hydrogensulfate/[Fe(HSO4)3*SiO2] In neat (no solvent) at 20℃; for 0.266667h; regioselective reaction; | 100% |
In ethanol Heating; |
Conditions | Yield |
---|---|
In ethanol at 20℃; for 4h; Reflux; | 100% |
In ethanol for 1h; Heating; | 69% |
In benzene for 24h; Ambient temperature; |
3,4,5-trimethoxy-benzaldehyde
Trimethylenediamine
N,N'-bis-(3,4,5-trimethoxybenzylidene)-1,3-diaminopropane
Conditions | Yield |
---|---|
In methanol for 1h; Ambient temperature; | 100% |
In ethanol for 1h; Heating; | 59% |
In methanol at 20℃; |
4-methoxy-benzaldehyde
Trimethylenediamine
N,N′-bis[(4-methoxyphenyl)methlylidene]propane-1,3-diamine
Conditions | Yield |
---|---|
In ethanol at 20℃; for 4h; Reflux; | 100% |
In ethanol at 20℃; for 4h; | 96.2% |
In methanol for 2h; Reflux; | 90% |
salicylaldehyde
Trimethylenediamine
N,N'-propane-1,3-diylbis(salicylideneimine)
Conditions | Yield |
---|---|
In ethanol at 20℃; for 4h; Reflux; | 100% |
In methanol at 20℃; for 0.5h; | 97% |
In ethanol | 97% |
di-tert-butyl dicarbonate
Trimethylenediamine
N-Boc-1,3-diaminopropane
Conditions | Yield |
---|---|
In chloroform 1.) 3 h, ice bath, 2.) room temperature, 16 h; | 100% |
In dichloromethane at 0 - 20℃; for 3h; Inert atmosphere; | 100% |
In 1,4-dioxane for 20h; Ambient temperature; | 98% |
2-Hydroxy-5-methylisophthalaldehyde
Trimethylenediamine
N,N'-propylenebis(3-formyl-5-methylsalicylaldimine)
Conditions | Yield |
---|---|
100% | |
In isopropyl alcohol at 20℃; for 1h; | 47% |
In ethanol Heating; |
Trimethylenediamine
8-bromo-2',3'-O-isopropylene adenosine
{(3aR,4R,6R,6aR)-6-[6-Amino-8-(3-amino-propylamino)-purin-9-yl]-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl}-methanol
Conditions | Yield |
---|---|
In water at 120℃; | 100% |
Conditions | Yield |
---|---|
With sodium hypochlorite In water at -5 - 20℃; for 13h; | 100% |
With sodium hydroxide; sodium hypochlorite In water at 20℃; for 6h; | 80% |
With sodium hypochlorite In water at 0 - 5℃; | |
With tert-butylhypochlorite In methanol at -5 - 5℃; for 24h; |
Trimethylenediamine
ethyl 2-cyanoacetate
2-cyano-N-[3-(2-cyanoacetylamino)propyl]acetamide
Conditions | Yield |
---|---|
100% | |
for 24h; Ambient temperature; | 90% |
at 20℃; for 1h; | 88% |
Trimethylenediamine
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 70℃; | 100% |
11-chloro-10H-indolo-[3,2-b]quinoline
Trimethylenediamine
N1-(10H-indolo[3,2-b]quinolin-11-yl)propane-1,3-diamine
Conditions | Yield |
---|---|
With hydrogenchloride In 2-ethoxy-ethanol for 15h; Heating; | 100% |
Stage #1: 11-chloro-10H-indolo-[3,2-b]quinoline; Trimethylenediamine With hydrogenchloride In 2-ethoxy-ethanol; water for 17h; Reflux; Stage #2: With potassium hydroxide In 2-ethoxy-ethanol; water Cooling with ice; | 75.7% |
(-)-dimethy-2,3-O-isopropylidene-L-tartrate
Trimethylenediamine
(4R,5R)-2,2-Dimethyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[(3-amino-propyl)-amide]
Conditions | Yield |
---|---|
In methanol for 216h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
In ethanol epoxide:amine=2:1; | 100% |
Trimethylenediamine
(2S,4R)-4-(methanesulfonyloxy)-2-[(methanesulfonyloxy)methyl]pyrrolidine-1-carboxylic acid tert-butyl ester
(1S,4S)-5-(3-aminopropyl)-2-(tert-butoxycarbonyl)-2,5-diazabicyclo[2.2.1]heptane
Conditions | Yield |
---|---|
4 h, 60 deg C, 8 h; | 100% |
(+)-dimethyl-2,3-O-isopropylidene-D-tartrate
Trimethylenediamine
Conditions | Yield |
---|---|
at 20℃; for 5.5h; Acylation; | 100% |
at 20℃; for 5.5h; |
4,7-dichloroquinoline
Trimethylenediamine
N-(7-chloroquinolin-4-yl)propane-1,3-diamine
Conditions | Yield |
---|---|
In neat (no solvent) at 110℃; | 100% |
Inert atmosphere; | 100% |
In isopropyl alcohol at 100℃; for 20h; | 98% |
5-hexynoic acid ethyl ester
Trimethylenediamine
N-(3-aminopropyl)hex-5-ynamide
Conditions | Yield |
---|---|
at 60℃; for 48h; | 100% |
(3aS,4S,6R,6aS)-2,2-dimethyl-6-vinyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol
Trimethylenediamine
Conditions | Yield |
---|---|
100% |
Trimethylenediamine
Conditions | Yield |
---|---|
Stage #1: 3β-(4'-chlorophenyl)tropane-2β-carboxylic acid With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine In dichloromethane at 0℃; for 0.166667h; Stage #2: Trimethylenediamine In dichloromethane at 20℃; | 100% |
Trimethylenediamine
Conditions | Yield |
---|---|
In ethanol; water at 70℃; for 24h; | 100% |
Conditions | Yield |
---|---|
With silica-supported ferric hydrogensulfate/[Fe(HSO4)3*SiO2] In neat (no solvent) at 20℃; for 0.2h; regioselective reaction; | 100% |
zirconium(IV) chloride at 20℃; for 0.25h; | 95% |
With sulfated zirconia at 20℃; for 0.416667h; | 92% |
(3α,5β)-3,24-bis(3-bromophenoxy)cholane
Trimethylenediamine
N1-[3-((R)-4-{(3S,5R,8R,9S,10S,13R,14S,17R)-3-[3-(3-Amino-propylamino)-phenoxy]-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl}-pentyloxy)-phenyl]-propane-1,3-diamine
Conditions | Yield |
---|---|
With 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane Heating; | 100% |
With 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; [Pd(dibenzylideneacetone)2] In 1,4-dioxane for 5h; Heating; | 60 % Spectr. |
Conditions | Yield |
---|---|
With acetic acid In ethanol Heating; | 100% |
In methanol; N,N-dimethyl-formamide for 4h; Heating; | 94% |
With acetic acid In methanol for 12h; Reflux; | 85.32% |
Conditions | Yield |
---|---|
In methanol at 20℃; for 120h; | 100% |
Conditions | Yield |
---|---|
In methanol at 20℃; for 72h; | 100% |
titanium
phosphoric acid
water
Trimethylenediamine
Conditions | Yield |
---|---|
In neat (no solvent) Ti:1,3-diaminopropane:H3PO4:H2O ratio = 2:2.21:13.65:500, autoclave, pH=2, 170°C (1 d, autogenous pressure); washing (water, alcohol and acetone); elem. anal.; | 100% |
With boric acid; HF In neat (no solvent) Ti:boric acid:H3PO4:1,3-diaminopropane:HF:H2O ratio = 1:6.54:13.65:2.21:3.36:600; |
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