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Looking for 107-06-2 / Ethylene Dichloride API manufacturers, exporters & distributors?

Ethylene Dichloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Ethylene Dichloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ethylene Dichloride manufacturer or Ethylene Dichloride supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethylene Dichloride manufacturer or Ethylene Dichloride supplier.

PharmaCompass also assists you with knowing the Ethylene Dichloride API Price utilized in the formulation of products. Ethylene Dichloride API Price is not always fixed or binding as the Ethylene Dichloride Price is obtained through a variety of data sources. The Ethylene Dichloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Ethylene Dichloride

Synonyms

107-06-2, Ethylene chloride, Ethane, 1,2-dichloro-, Glycol dichloride, Dichloroethylene, Dutch liquid

Cas Number

107-06-2

Unique Ingredient Identifier (UNII)

55163IJI47

About Ethylene Dichloride

Ethylene Dichloride is a clear, colorless, oily, synthetic, flammable liquid chlorinated hydrocarbon with a pleasant chloroform-like smell that emits toxic fumes of hydrochloric acid when heated to decomposition. Ethylene dichloride is primarily used to produce vinyl chloride. Inhalation exposure to this substance induces respiratory distress, nausea and vomiting and affects the central nervous system, liver and kidneys. It is mutagenic in animals and is reasonably anticipated to be a human carcinogen. (NCI05)

03530_FLUKA Manufacturers

A 03530_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 03530_FLUKA, including repackagers and relabelers. The FDA regulates 03530_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 03530_FLUKA API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

03530_FLUKA Suppliers

A 03530_FLUKA supplier is an individual or a company that provides 03530_FLUKA active pharmaceutical ingredient (API) or 03530_FLUKA finished formulations upon request. The 03530_FLUKA suppliers may include 03530_FLUKA API manufacturers, exporters, distributors and traders.

click here to find a list of 03530_FLUKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

03530_FLUKA USDMF

A 03530_FLUKA DMF (Drug Master File) is a document detailing the whole manufacturing process of 03530_FLUKA active pharmaceutical ingredient (API) in detail. Different forms of 03530_FLUKA DMFs exist exist since differing nations have different regulations, such as 03530_FLUKA USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 03530_FLUKA DMF submitted to regulatory agencies in the US is known as a USDMF. 03530_FLUKA USDMF includes data on 03530_FLUKA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 03530_FLUKA USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 03530_FLUKA suppliers with USDMF on PharmaCompass.

03530_FLUKA GMP

03530_FLUKA Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of 03530_FLUKA GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right 03530_FLUKA GMP manufacturer or 03530_FLUKA GMP API supplier for your needs.

03530_FLUKA CoA

A 03530_FLUKA CoA (Certificate of Analysis) is a formal document that attests to 03530_FLUKA's compliance with 03530_FLUKA specifications and serves as a tool for batch-level quality control.

03530_FLUKA CoA mostly includes findings from lab analyses of a specific batch. For each 03530_FLUKA CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

03530_FLUKA may be tested according to a variety of international standards, such as European Pharmacopoeia (03530_FLUKA EP), 03530_FLUKA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (03530_FLUKA USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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