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Looking for 822-06-0, 11142-52-2 / Hexamethylene Diisocyanate API manufacturers, exporters & distributors?

Hexamethylene Diisocyanate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Hexamethylene Diisocyanate 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 Hexamethylene Diisocyanate manufacturer or Hexamethylene Diisocyanate supplier for your needs.

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

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

API | Excipient name

Hexamethylene Diisocyanate

Synonyms

1,6-diisocyanatohexane, 822-06-0, 1,6-hexamethylene diisocyanate, Hmdi, Hexane, 1,6-diisocyanato-, Hexane 1,6-diisocyanate

Cas Number

822-06-0, 11142-52-2

Unique Ingredient Identifier (UNII)

0I70A3I1UF

About Hexamethylene Diisocyanate

Hexamethylene diisocyanate is used as a polymerizing agent in polyurethane paints and coatings. Acute (short-term) exposure to high concentrations of hexamethylene diisocyanate in humans can cause pulmonary edema, coughing, and shortness of breath. Hexamethylene diisocyanate is also extremely irritating to the eyes, nose, and throat. Human studies have suggested that chronic (long-term) exposure to hexamethylene diisocyanate may cause chronic lung problems. Animal studies have reported respiratory effects from chronic inhalation exposure and skin irritation and sensitization from dermal exposure to hexamethylene diisocyanate. No information is available on the reproductive, developmental, or carcinogenic effects of hexamethylene diisocyanate in humans. EPA has not classified hexamethylene diisocyanate for carcinogenicity.

Tox21_300161 Manufacturers

A Tox21_300161 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300161, including repackagers and relabelers. The FDA regulates Tox21_300161 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300161 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Tox21_300161 Suppliers

A Tox21_300161 supplier is an individual or a company that provides Tox21_300161 active pharmaceutical ingredient (API) or Tox21_300161 finished formulations upon request. The Tox21_300161 suppliers may include Tox21_300161 API manufacturers, exporters, distributors and traders.

Tox21_300161 GMP

Tox21_300161 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 Tox21_300161 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 Tox21_300161 GMP manufacturer or Tox21_300161 GMP API supplier for your needs.

Tox21_300161 CoA

A Tox21_300161 CoA (Certificate of Analysis) is a formal document that attests to Tox21_300161's compliance with Tox21_300161 specifications and serves as a tool for batch-level quality control.

Tox21_300161 CoA mostly includes findings from lab analyses of a specific batch. For each Tox21_300161 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.

Tox21_300161 may be tested according to a variety of international standards, such as European Pharmacopoeia (Tox21_300161 EP), Tox21_300161 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tox21_300161 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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