Hangzhou Verychem Science And Technology Co. Ltd. was set up in year 2004, it’s a young but fast growing company. In the twelve years history, it invested two pharmaceutical raw material production plants, one researching company, and several
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inquiryProduct Description Product Name 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride CAS No. 25952-53-8 Appearance White powder Assay ≥99% Capacity 200mt/year
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inquiryItems Standard Result Appearance White crystalline powder Complies Assay(AT) 98%-102%
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inquiryUnique advantages Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White crystalline powder Storage:cool dry place Package:25kg/drum Application:fine chemical Transportation:by cou
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inquiryHebei yanxi chemical co. LTD. has expanded a compositive entity from initially only as a small manufacturer. The company dedicated to the development, production and marketing of chemicals. After many years of efforts, we have established stable
1-(3-Dimethylaminopropyl)-3-Ethyl Carbodiimide Hydrochloride [CAS:25952-53-8] EDC.HCl for Argatroban Name 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride Synonyms N'-(ethylcarbonimidoyl)-N,N-dimethyl
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inquiryhigh 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
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inquiry1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience2. Free samples will be provided,ensure specifications and quality are right for customer3. Customers will receive the most professional technical s
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Name:1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride CAS NO: 25952-53-8 Grade:Medical scientific research and export Molecular formula:C7H18ClN3 Molecular weight:179.6909 Product Quality 12 years of chemical raw materials Mature
Cas:25952-53-8
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inquiryProduct Name: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride Synonyms: (3-dimethylaminopropyl)ethyl-carbodiimidmonohydrochloride;3-propanediamine,n’-(ethylcarbonimidoyl)-n,n-dimethyl-monohydrochloride;1-(3-Dimethylaminopropyl)-3
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inquiryTest Standard Results Appearance
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inquiryName: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride Synonyms: 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide Hydrochloride CAS: 25952-53-8 MF: C7H18ClN3 Appearance:White powder Storage:Store in cool and dry place, away from sun light
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inquiryAppearance:White crystalline powder Storage:R.T Package:25kg/drum Application:Polypeptide Condensing Agent Transportation:Express/Sea/Air Port:Any port in China
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inquiryN-(3-dimethylaminopropyl)-N-ethylcarbodiimide
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
With triethylamine hydrochloride In acetonitrile at 15℃; for 1h; Temperature; | 92% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride at 90℃; for 42h; | 66% |
pyridine hydrochloride
N-(3-dimethylaminopropyl)-N-ethylcarbodiimide
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
In dichloromethane at 30℃; Solvent; Temperature; | 71.2 g |
N-(3-Dimethylamino-propyl)-dithiocarbamidsaeure
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: chloroformic acid ethyl ester; triethylamine / dichloromethane / 3 h / 10 - 15 °C 2: dichloromethane / 1 h / 10 - 15 °C 3: sodium hypochlorite; ethylenediaminetetraacetic acid / 30 °C 4: dichloromethane / 30 °C View Scheme |
3-(dimethylamino)propyl isothiocyanate
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: dichloromethane / 1 h / 10 - 15 °C 2: sodium hypochlorite; ethylenediaminetetraacetic acid / 30 °C 3: dichloromethane / 30 °C View Scheme |
1-amino-3-(dimethylamino)propane
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: methanol / 2 h / 10 - 20 °C 2: chloroformic acid ethyl ester; triethylamine / dichloromethane / 3 h / 10 - 15 °C 3: dichloromethane / 1 h / 10 - 15 °C 4: sodium hypochlorite; ethylenediaminetetraacetic acid / 30 °C 5: dichloromethane / 30 °C View Scheme |
5-(4-Methoxyphenyl)-4-(6-methoxy-3-pyridinyl)-1,3-oxazole-2-carboxylic acid
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
With benzotriazol-1-ol In DMF (N,N-dimethyl-formamide) at 0℃; for 18h; | 100% |
pyridinium p-toluenesulfonate
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
EDCI*TsOH
Conditions | Yield |
---|---|
With potassium carbonate In dichloromethane | 100% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
With water at 20℃; | 100% |
glycine ethyl ester hydrochloride
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
methyl hippurate
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; benzotriazol-1-ol; benzoic acid | 98% |
3-(5-methyl-1H-imidazol-1-yl)propan-1-amine
(4-ethylphenyl)isothiocyanate
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
2-cyano(4-ethylphenyl)-3-(3-(5-methyl-1H-imidazol-1-yl)propyl)guanidine
Conditions | Yield |
---|---|
With sodium cyanamide In ethanol; N,N-dimethyl-formamide at 20℃; for 6h; Heating / reflux; | 96.7% |
(S)-2-{(S)-2-[(S)-2-((S)-2-Benzyloxycarbonylamino-2-methyl-pentanoylamino)-2-methyl-pentanoylamino]-2-methyl-pentanoylamino}-2-methyl-pentanoic acid
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 3h; | 95% |
2-[2-(2-methoxyethoxy)ethoxy]ethylamine
protoporphyrin IX
benzotriazol-1-ol
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
Stage #1: protoporphyrin IX; benzotriazol-1-ol In N,N-dimethyl-formamide at 0℃; for 0.666667h; Inert atmosphere; Stage #2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0℃; for 1h; Inert atmosphere; Stage #3: 2-[2-(2-methoxyethoxy)ethoxy]ethylamine In N,N-dimethyl-formamide at 0 - 20℃; for 28h; Inert atmosphere; | 95% |
2,2-difluorobenzo[d][1,3]dioxole-5,6-diamine
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 95% |
2-amino-3-methylphenol
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 95% |
4-(tert-butyl)-1,2-diaminobenzene
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 94% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
2-amino-4-tert-butylphenol
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 94% |
2-amino-4-bromobenzenethiol
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 94% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Benzoyl isothiocyanate
N-((4S,6S)-4-(2-chloro-3-fluorophenyl)-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-yl)benzamide
Conditions | Yield |
---|---|
With hydrogenchloride; triethylamine In tetrahydrofuran; 1,4-dioxane; methanol; ethyl acetate | 93% |
tetradecylamine
10,12-docosadiynedioic acid
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
B
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide
Conditions | Yield |
---|---|
With dmap In chloroform at 25℃; for 20h; | A 92.6% B n/a |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
With sodium hydrogensulfite; sodium hydroxide In water at 20℃; for 4h; pH=6.8; | 92% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
In water for 1h; Ambient temperature; pH=4.75; | 91.4% |
Sarcosine ethyl ester
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
With benzotriazol-1-ol In chloroform; water; ethyl acetate; N,N-dimethyl-formamide | 91% |
m-formylphenyl benzoic acid
(1S)-2-(3,5-dichloro-1-oxido-pyridin-1-ium-4-yl)-1-(3,4-dimethoxyphenyl)ethanol
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
With dmap | 91% |
N-ethylaminoxyacetamide
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
In dichloromethane | 90% |
4-chloro-aniline
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
Stage #1: (3S,4S)-4-(4-bromophenyl)-1-methyl-pyrrolidine-3-carboxylic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride With benzotriazol-1-ol In N,N-dimethyl-formamide at 20℃; for 4h; Stage #2: 4-chloro-aniline In N,N-dimethyl-formamide at 50℃; for 2h; | A 90% B n/a C n/a |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
1,2-diamino-benzene
N-ethyl-1H-benzo[d]imidazol-2-amine
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Solvent; Temperature; Wavelength; Microwave irradiation; | 90% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
2-amino-phenol
N-ethylbenzo[d]oxazol-2-amine
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 90% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
2-amino-6-methylphenol
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 90% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
2-amino-benzenethiol
2-ethylaminobenzothiazole
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 90% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
N-methyl-1,2-phenylenediamine
N-ethyl-1-methyl-1H-benzo[d]imidazol-2-amine
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 89% |
dmap
1-dodecyl alcohol
N-Cbz-L-Asp
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
C36H61NO6
Conditions | Yield |
---|---|
Stage #1: N-Cbz-L-Asp; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0℃; for 0.5h; Stage #2: dmap; 1-dodecyl alcohol at 20℃; for 24h; | 88% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
4-Bromo-benzene-1,2-diamine
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 88% |
2,3-Diaminonaphthalene
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 88% |
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride
3-Amino-2-naphthol
Conditions | Yield |
---|---|
In isopropyl alcohol at 80℃; for 0.25h; Microwave irradiation; | 88% |
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