Page last updated: 2024-12-07

1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide methiodide

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## 1-Ethyl-3-(3-(dimethylamino)propyl)carbodiimide methiodide (EDC·HCl)

**What it is:**

1-Ethyl-3-(3-(dimethylamino)propyl)carbodiimide methiodide (EDC·HCl) is a chemical compound commonly used in research as a **carbodiimide coupling reagent**. It's a water-soluble, white crystalline solid that is generally used as a **catalyst** for the formation of **amide bonds**.

**Why it's important for research:**

EDC·HCl plays a crucial role in a wide range of research areas, particularly in:

* **Biochemistry:** EDC·HCl is used to **couple proteins, peptides, and other biomolecules**, which is essential for studying their interactions and creating new bioconjugates. This helps in the development of antibodies, vaccines, and other therapeutic agents.
* **Materials Science:** EDC·HCl is used to **modify surfaces and create functional materials**. This allows for the development of new biocompatible materials, sensors, and drug delivery systems.
* **Chemical Synthesis:** EDC·HCl is used to **synthesize various organic compounds**, including peptides, amides, and esters. Its ability to catalyze amide bond formation is valuable in developing new drugs and polymers.
* **Molecular Biology:** EDC·HCl is used to **crosslink DNA and proteins**, allowing researchers to study their interactions and understand biological processes.

**Mechanism of action:**

EDC·HCl acts as a **dehydrating agent**, removing water molecules from the reaction mixture and promoting the formation of amide bonds between carboxyl and amine groups. This reaction is highly efficient and specific, making EDC·HCl a valuable tool for bioconjugation and chemical synthesis.

**Advantages of EDC·HCl:**

* **High efficiency and selectivity:** EDC·HCl promotes the formation of amide bonds with high efficiency and specificity, minimizing side reactions.
* **Water-solubility:** EDC·HCl is water-soluble, making it compatible with various biological and aqueous reaction systems.
* **Mild reaction conditions:** EDC·HCl can be used under relatively mild conditions, making it suitable for sensitive biomolecules.

**Limitations of EDC·HCl:**

* **Toxicity:** EDC·HCl can be toxic and requires careful handling and disposal.
* **Hydrolysis:** EDC·HCl can be hydrolyzed in water, decreasing its effectiveness.
* **Side reactions:** While EDC·HCl is generally highly specific, it can still undergo side reactions with other functional groups.

**Overall:**

EDC·HCl is a versatile and powerful tool in various research areas, enabling scientists to study and modify biomolecules, synthesize new compounds, and develop advanced materials. Its importance lies in its ability to promote the formation of amide bonds with high efficiency and specificity, making it an essential reagent for a range of applications.

Cross-References

ID SourceID
PubMed CID122242
SCHEMBL ID1092039
MeSH IDM0123852

Synonyms (45)

Synonym
nsc-282762
22572-40-3
nsc282762
1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide methiodide
edc methiodide
AKOS009156884
3-(ethyliminomethylideneamino)propyl-trimethyl-azanium iodide
3-(ethyliminomethylideneamino)propyl-trimethylammonium iodide
A816570
(3-((ethylimidocarbonyl)amino)propyl)trimethylammonium iodide
1-propanaminium, 3-(ethylcarbonimidoylamino)-n,n,n-trimethyl-, iodide
1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide methiodide
nsc 282762
73u5123rnt ,
einecs 245-095-1
unii-73u5123rnt
FT-0607745
1-propanaminium, 3-((ethylcarbonimidoyl)amino)-n,n,n-trimethyl-, iodide (1:1)
n-(3-(dimethylamino)propyl)-n'-ethylcarbodiimide methiodide
1-ethyl-3-(3-(trimethylammonio)propyl)carbodiimide iodide
1-(3-(dimethylamino)propyl)-3-ethylcarbodiimide methiodide
1-propanaminium, 3-((ethylcarbonimidoyl)amino)-n,n,n-trimethyl-, iodide
edc methiodide [mi]
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide methiodide
ammonium, (3-((ethylimidocarbonyl)amino)propyl)trimethyl-, iodide
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide methiodide
1-[3-(dimethyamino)propyl]-3-ethyl carbodiimide methiodide
3-{[(ethylimino)methylidene]amino}-n,n,n-trimethyl-1-propanaminium iodide
AGSKWMRPXWHSPF-UHFFFAOYSA-M
SCHEMBL1092039
J-503138
J-670020
mfcd00011833
J-801019
F0001-0796
3-(((ethylimino)methylene)amino)-n,n,n-trimethylpropan-1-aminium iodide
CS-0204286
3-{[(ethylimino)methylidene]amino}-n,n,n-trimethylpropan-1-aminium iodide
DTXSID20945227
D5334
EN300-36735
(3-{[(ethylimino)methylidene]amino}propyl)trimethylazanium iodide
3-((ethylimino)methyleneamino)-n,n,n-trimethylpropan-1-aminium iodide
D90385
Q27266208
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (49)

TimeframeStudies, This Drug (%)All Drugs %
pre-199013 (26.53)18.7374
1990's16 (32.65)18.2507
2000's18 (36.73)29.6817
2010's2 (4.08)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.35

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index10.35 (24.57)
Research Supply Index3.97 (2.92)
Research Growth Index4.32 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.35)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other52 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]