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Looking for 2694-54-4 / Triallyl Trimellitate API manufacturers, exporters & distributors?

Triallyl Trimellitate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Triallyl Trimellitate 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 Triallyl Trimellitate manufacturer or Triallyl Trimellitate supplier for your needs.

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

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

API | Excipient name

Triallyl Trimellitate

Synonyms

2694-54-4, Triallyl benzene-1,2,4-tricarboxylate, 1,2,4-benzenetricarboxylic acid, tri-2-propenyl ester, Trimellitic acid triallyl ester, 1,2,4-triallyl trimellitate, Triallyl 1,2,4-benzenetricarboxylate

Cas Number

2694-54-4

Unique Ingredient Identifier (UNII)

4MJD3RL023

Triallyl Trimellitate Manufacturers

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

Triallyl Trimellitate Suppliers

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

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

Triallyl Trimellitate USDMF

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

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

click here to find a list of Triallyl Trimellitate suppliers with USDMF on PharmaCompass.

Triallyl Trimellitate GMP

Triallyl Trimellitate 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 Triallyl Trimellitate 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 Triallyl Trimellitate GMP manufacturer or Triallyl Trimellitate GMP API supplier for your needs.

Triallyl Trimellitate CoA

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

Triallyl Trimellitate CoA mostly includes findings from lab analyses of a specific batch. For each Triallyl Trimellitate 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.

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