1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride | EDC HCL Manufacturer | India

1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride (EDC HCl) is one of the most widely used coupling reagents in organic and peptide synthesis. Known for its efficiency, water solubility, and reliability, EDC HCl plays a crucial role in forming amide and ester bonds, making it a key component in bioconjugation, pharmaceutical research, and industrial chemistry.

At LifeChemPharma, we are a leading EDC HCl manufacturer in India, supplying high-purity products to pharmaceutical, biotechnology, and research industries across the globe, including Italy, Europe, and Asia.

What is EDC HCl?

Chemical Name: 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride
Molecular Formula: C8H17N3·HCl
Molecular Weight: 191.70 g/mol
CAS Number: 25952-53-8

EDC HCl is a water-soluble carbodiimide used to activate carboxyl groups for coupling reactions with amines, forming stable amide linkages. Unlike other coupling reagents, EDC HCl does not introduce additional unwanted byproducts and is compatible with both aqueous and organic systems.

Key Applications of EDC HCl

Peptide Synthesis
1. Facilitates peptide bond formation between amino acids with high yields.
2. Preferred in pharmaceutical peptide manufacturing and research.
Bioconjugation and Crosslinking
1. Used to link proteins, antibodies, and enzymes to various substrates in biotechnology and diagnostics.
Pharmaceutical and Fine Chemicals
1. Acts as an efficient coupling agent in drug development and intermediate synthesis.
Material Science and Nanotechnology
1. Plays a role in surface modification, creating functionalized nanomaterials.

LifeChemPharma – Reliable EDC HCl Manufacturer in India

As a trusted name in the global chemical industry, LifeChemPharma focuses on manufacturing, scaling, and supplying high-quality EDC HCl.

Our Strengths

High Purity & Consistency: Every batch undergoes stringent quality testing.
Custom Manufacturing: Tailored solutions based on customer requirements.
Regulatory Compliance: Produced under ISO and GMP-aligned standards.
Global Supply Capability: Efficient exports to Italy, Europe, and other international markets.

Our manufacturing infrastructure in India is equipped with modern analytical facilities, ensuring top-notch quality and performance consistency for EDC HCl used in sensitive applications.

Why Choose LifeChemPharma as Your EDC HCl Supplier?

✅ Experience in Carbodiimide Chemistry: Decades of expertise in synthesizing coupling agents.
✅ Global Reach: Supplying EDC HCl to pharmaceutical and chemical industries in India, Italy, Germany, and beyond.
✅ On-Time Delivery: Strong logistics and export support ensure fast and reliable shipments.
✅ Customer-Centric Approach: Technical support and documentation provided for smooth regulatory submission.

Specifications of 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride

ParameterSpecificationAppearanceWhite to off-white crystalline powderAssay (Purity)≥99%SolubilityWater, alcoholsStorageStore in a cool, dry place away from moisturePackaging25 kg HDPE drum / as per client requirement

Global Presence – India & Italy

LifeChemPharma has expanded its footprint beyond India, establishing strong export relationships across Europe, particularly in Italy, where demand for high-quality intermediates and coupling reagents is growing rapidly.

Our focus on quality assurance, technical documentation, and customer service has made LifeChemPharma a trusted partner for global pharmaceutical manufacturers and research organizations.

Commitment to Quality

Every batch of EDC HCl produced by LifeChemPharma undergoes rigorous quality control measures, including:

HPLC and GC analysis
Moisture and impurity testing
Stability and compatibility studies

We ensure compliance with international standards, supporting our clients in regulatory submissions and product development.

Conclusion

LifeChemPharma stands among the leading 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride (EDC HCl) manufacturers in India, with a growing global presence, including exports to Italy and other European countries.

With our focus on purity, quality, and customer satisfaction, we are committed to empowering pharmaceutical innovation and chemical manufacturing through reliable supply and technical excellence.

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4-tert-Butylthiophenol: A Valuable Aromatic Thiol for Organic and Material Chemistry

4-tert-Butylthiophenol is a specialized aromatic thiol widely used in organic synthesis, materials science, and surface modification. This compound is known for its unique sulfur functionality combined with a sterically hindered tert-butyl group, making it a versatile reagent and intermediate in chemical industries.

2-bromophenol

[url=https://www.lifechempharma.com/product/2-bromophenol-manufacturer/]2-bromophenol-manufacturer[/url] is an aromatic halogenated phenol compound commonly used as a building block in organic synthesis. It is an ortho-substituted bromophenol, where a bromine atom is attached to the benzene ring at the second position relative to the hydroxyl group (-OH). The presence of both hydroxyl and halogen groups makes it a versatile reagent in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Chemical Structure and Properties Property Description Chemical Name 2-Bromophenol Molecular Formula C₆H₅BrO Molecular Weight 173.01 g/mol CAS Number 95-56-7 Appearance White to pale yellow crystalline solid Boiling Point 210°C Melting Point 7°C Density 1.77 g/cm³ Solubility Slightly soluble in water, soluble in organic solvents like ethanol, ether, and chloroform Chemical Structure The structure of 2-bromophenol consists of a benzene ring with two functional groups: Hydroxyl group (-OH) at the first position. Bromine atom (Br) at the second position (ortho position). This combination gives the molecule unique chemical and physical properties, including polarity, reactivity, and solubility. Synthesis of 2-Bromophenol 2-Bromophenol can be synthesized by: Bromination of Phenol: Phenol undergoes electrophilic aromatic substitution with bromine in the presence of a catalyst (like FeBr₃), resulting in bromophenol. By controlling the reaction conditions, the ortho isomer (2-bromophenol) can be selectively produced. Reaction: C 6 H 5 OH + Br 2 → C 6 H 4 BrOH + HBr C 6 H 5 OH+Br 2 →C 6 H 4 BrOH+HBr Direct Bromination with NBS (N-Bromosuccinimide): NBS is used as a brominating agent in the presence of a radical initiator (like light or peroxide) to selectively brominate phenol derivatives at the ortho position. Applications of 2-Bromophenol Intermediate in Pharmaceutical Synthesis: 2-Bromophenol is a key starting material in the production of antifungal agents, analgesics, and anti-inflammatory drugs. It is used to prepare brominated benzodiazepines and other heterocyclic compounds. Building Block in Organic Synthesis: It is used as a precursor for the synthesis of aryl ethers, aryl amines, and aryl halides. The hydroxyl and bromine groups facilitate substitution and coupling reactions, such as: Suzuki coupling Buchwald-Hartwig amination Ullmann reaction Agrochemical Synthesis: Used in the preparation of fungicides, herbicides, and pesticides. Polymer Chemistry: It is employed in the modification of polymers and resins, improving their chemical and thermal properties. Dye and Pigment Manufacturing: The compound is used in the synthesis of azo dyes and organic pigments. Biochemical Studies: It serves as a model compound in studying the interaction of phenolic compounds with biological systems, particularly their role in enzyme inhibition and antioxidant activity. Reactivity of 2-Bromophenol 2-Bromophenol exhibits both nucleophilic and electrophilic reactivity due to the presence of the hydroxyl and bromine groups: Nucleophilic Substitution (SNAr): The bromine atom can be displaced by a nucleophile (e.g., amine, thiol, or alkoxide) to form various derivatives. Electrophilic Substitution: The hydroxyl group activates the benzene ring, making it more susceptible to further electrophilic substitutions, such as nitration, sulfonation, or alkylation. Oxidation: The hydroxyl group can be oxidized to form quinones or other oxidized phenol derivatives. Safety and Handling 2-Bromophenol is classified as a hazardous substance and should be handled with care. Hazards: Causes skin and eye irritation. Harmful if inhaled or ingested. Can cause environmental damage if released into water bodies. Precautions: Wear PPE: Gloves, goggles, and a lab coat should be worn while handling. Work in a fume hood: Avoid inhaling vapors. Proper storage: Keep in a cool, dry place, away from heat, moisture, and incompatible substances (e.g., strong oxidizers). First Aid Measures: Skin contact: Wash thoroughly with soap and water. Eye contact: Rinse with water for at least 15 minutes and seek medical attention. Inhalation: Move to fresh air immediately and seek medical help if symptoms persist. Environmental Impact 2-Bromophenol can be toxic to aquatic life and should not be released into the environment. Proper waste disposal methods must be followed in compliance with local regulations. Conclusion 2-Bromophenol is a valuable reagent in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its unique structure and reactivity make it an important intermediate in various chemical transformations. While it is a useful compound, appropriate safety precautions should be taken to handle it safely due to its hazardous properties.

1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride | EDC HCL Manufacturer | India | Italy

What is EDC HCl?

Key Applications of EDC HCl

LifeChemPharma – Reliable EDC HCl Manufacturer in India

Our Strengths

Why Choose LifeChemPharma as Your EDC HCl Supplier?

Specifications of 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride

Global Presence – India & Italy

Commitment to Quality

Conclusion

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4-tert-Butylthiophenol: A Valuable Aromatic Thiol for Organic and Material Chemistry

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2-bromophenol

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1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride | EDC HCL Manufacturer | India | Italy

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