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Looking for 21245-02-3 / 2-Ethylhexyl 4-(Dimethylamino)Benzoate API manufacturers, exporters & distributors?

2-Ethylhexyl 4-(Dimethylamino)Benzoate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of 2-Ethylhexyl 4-(Dimethylamino)Benzoate 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 2-Ethylhexyl 4-(Dimethylamino)Benzoate manufacturer or 2-Ethylhexyl 4-(Dimethylamino)Benzoate supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 2-Ethylhexyl 4-(Dimethylamino)Benzoate manufacturer or 2-Ethylhexyl 4-(Dimethylamino)Benzoate supplier.

PharmaCompass also assists you with knowing the 2-Ethylhexyl 4-(Dimethylamino)Benzoate API Price utilized in the formulation of products. 2-Ethylhexyl 4-(Dimethylamino)Benzoate API Price is not always fixed or binding as the 2-Ethylhexyl 4-(Dimethylamino)Benzoate Price is obtained through a variety of data sources. The 2-Ethylhexyl 4-(Dimethylamino)Benzoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

2-Ethylhexyl 4-(Dimethylamino)Benzoate

Synonyms

21245-02-3, Padimate o, 2-ethylhexyl 4-dimethylaminobenzoate, Padimate-o, Escalol 507, Octyl dimethyl paba

Cas Number

21245-02-3

Unique Ingredient Identifier (UNII)

Z11006CMUZ

About 2-Ethylhexyl 4-(Dimethylamino)Benzoate

Padimate O is an active sunscreen agent in cosmetics and over-the-counter sunscreen drug products in concentrations up to 8%, as regulated by the FDA. It is a structurally-related compound to [DB02362] that absorbs UV-B rays to prevent photodamage. It penetrates human skin, and is shown to induce non-ligatable strand breaks on DNA in vitro and mutagenic effects on yeast in vivo.

PreSun 23 (Salt/Mix) Manufacturers

A PreSun 23 (Salt/Mix) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PreSun 23 (Salt/Mix), including repackagers and relabelers. The FDA regulates PreSun 23 (Salt/Mix) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PreSun 23 (Salt/Mix) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

PreSun 23 (Salt/Mix) Suppliers

A PreSun 23 (Salt/Mix) supplier is an individual or a company that provides PreSun 23 (Salt/Mix) active pharmaceutical ingredient (API) or PreSun 23 (Salt/Mix) finished formulations upon request. The PreSun 23 (Salt/Mix) suppliers may include PreSun 23 (Salt/Mix) API manufacturers, exporters, distributors and traders.

PreSun 23 (Salt/Mix) GMP

PreSun 23 (Salt/Mix) 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 PreSun 23 (Salt/Mix) 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 PreSun 23 (Salt/Mix) GMP manufacturer or PreSun 23 (Salt/Mix) GMP API supplier for your needs.

PreSun 23 (Salt/Mix) CoA

A PreSun 23 (Salt/Mix) CoA (Certificate of Analysis) is a formal document that attests to PreSun 23 (Salt/Mix)'s compliance with PreSun 23 (Salt/Mix) specifications and serves as a tool for batch-level quality control.

PreSun 23 (Salt/Mix) CoA mostly includes findings from lab analyses of a specific batch. For each PreSun 23 (Salt/Mix) 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.

PreSun 23 (Salt/Mix) may be tested according to a variety of international standards, such as European Pharmacopoeia (PreSun 23 (Salt/Mix) EP), PreSun 23 (Salt/Mix) JP (Japanese Pharmacopeia) and the US Pharmacopoeia (PreSun 23 (Salt/Mix) 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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