<Suppliers Price>

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride

Names

[ CAS No. ]:
25952-53-8

[ Name ]:
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride

[Synonym ]:
N-(3-(Dimethylamino)propyl)-N'-ethylcarbodiimide hydrochloride
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
Carbodiimide, (3-dimethylaminopropyl)ethyl-, monohydrochloride
EDC HCL
EDAC,Hydrochloride
N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride
N-(3-dimethylaminopropyl)-N′-ethyl-carbodiimide hydrochloride
Carbodiimide, [3-(dimethylamino)propyl]ethyl-, hydrochloride
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
N-Ethyl-N'-(3-dimethylaminopropyl)carbodiimide hydrochloride
1-Ethyl-3-[3-(dimethylamino)propyl]carbodiimide monohydrochloride
1-Ethyl-3-(3-dimethyllaminopropyl)carbodiimide hydrochloride
1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride
N'-(Ethylcarbonimidoyl)-N,N-dimethyl-1,3-propanediamine hydrochloride
N-[3-(Dimethylamino)propyl]-N'-ethylcarbodiimide hydrochloride
1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide monohydrochloride
N-Ethyl-N'-[3-(dimethylamino)propyl]carbodiimide hydrochloride
1,3-Propanediamine, N-(ethylcarbonimidoyl)-N,N-dimethyl-, hydrochloride (1:1)
1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride
EDCI
1-ethyl-3(3-dimethylaminopropyl) carbodiimide hydrochloride
EINECS 217-579-2
Carbodiimide, [3-(dimethylamino)propyl]ethyl-, monohydrochloride
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, hydrochloride
1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride [Coupling Agent
EDAP
N-[3-(Dimethylamino)propyl]-N'-ethylcarbodiimide hydrochloride (1:1)
Carbodiimide, (3-(dimethylamino)propyl)ethyl-, monohydrochloride
Carbodiimide, (3-dimethylaminopropyl)ethyl-, hydrochloride
3-(3-Dimethylaminopropyl)-1-Ethylcarbodiimide Hydrochloride
MFCD00044916
1-(3-(dimethylamino)-propyl)-3-ethylcarbodiimide hydrochloride
N1-((Ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride
EDC.HCl
EDC hydrochloride
edac hcl
wsc hcl
1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride
EDC·HCl
1-(3-DIMETHYLAMINOPROPYL)-3-ETHYLCARBODIIMIDE,EDC.HCl

Biological Activity

[Description]:

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride is a carbodiimide reagent that can form nucleic acid and compounds with amide bonds. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride accelerates the formation reaction of esters, amides, and peptides, as a condensing and dehydrating agent, which are often used for polynucleotide synthesis, anhydroxydation, lactonization and esterification[1][2].

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

[In Vitro]

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC.HCl) is a very useful agent to form amide bonds (peptide bonds) in an aqueous medium[1]. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC•HCl), is widely used for polyaniline-carbon nanotube preparation for a cholesterol biosensor, precolumn derivatization of aliphatic amines for HPLC, molecular beacons formation for DNA reseach, sensor preparation for calcium detection, the fluorescent determination of carboxylic acids, and solidphase microsequencing of peptides[2]. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC•HCl) is an aminoaldehyde dehydrogenase (AMADH) inhibitor, while its inhibition on glutamate decarboxylase (GAD) is insignificant[3].

[References]

[1]. Kunihiko Seno, et al. Spectrophotometric determination of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride by flow injection analysis. Anal Sci. 2008 Apr;24(4):505-8.

[2]. Kunihiko Seno, et al. Determination of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride by flow-injection analysis based on a specific condensation reaction between malonic acid and ethylenediamine. Anal Sci. 2009 Mar;25(3):389-93.

[3]. Runqiang Yang, et al. AMADH inhibitor optimization and its effects on GABA accumulation in soybean sprouts under NaCl-CaCl 2 treatment. 3 Biotech. 2019 May;9(5):184.

Chemical & Physical Properties

[ Density]:
0.877 g/mL at 20 °C(lit.)

[ Boiling Point ]:
269.1ºC at 760 mmHg

[ Melting Point ]:
110-115 °C(lit.)

[ Molecular Formula ]:
C8H18ClN3

[ Molecular Weight ]:
191.70

[ Flash Point ]:
107.9ºC

[ Exact Mass ]:
191.118927

[ PSA ]:
27.96000

[ LogP ]:
1.93390

[ Vapour Pressure ]:
0.171mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.461

[ Storage condition ]:
−20°C

[ Stability ]:
Stable, but sensitive to moisture. Incompatible with strong acids, strong oxidizing agents, moisture.

[ Water Solubility ]:
Soluble

MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H315-H318-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36/37/39-S45-S37/39

[ RIDADR ]:
UN 2735 8/PG 3

[ WGK Germany ]:
3

[ RTECS ]:
FF2200000

[ HS Code ]:
29252000

Precursor & DownStream

Customs

[ HS Code ]: 2925290090

[ Summary ]:
2925290090 other imines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Minimizing the non-specific binding of nanoparticles to the brain enables active targeting of Fn14-positive glioblastoma cells.

Biomaterials 42 , 42-51, (2014)

A major limitation in the treatment of glioblastoma (GBM), the most common and deadly primary brain cancer, is delivery of therapeutics to invading tumor cells outside of the area that is safe for sur...

Altering in vivo macrophage responses with modified polymer properties.

Biomaterials 56 , 187-97, (2015)

Macrophage reprogramming has long been the focus of research in disease therapeutics and biomaterial implantation. With different chemical and physical properties of materials playing a role in macrop...

Species-dependent binding of new synthesized bicalutamide analogues to albumin by optical biosensor analysis.

J. Pharm. Biomed. Anal. 111 , 324-32, (2015)

The binding of some novel bicalutamide analogues to human serum albumin (HSA) and rat serum albumin (RSA) was investigated by surface plasmon resonance (SPR) based optical biosensor technique. The ser...


More Articles


Related Compounds