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Looking for 100-51-6 / Benzyl Alcohol API API manufacturers, exporters & distributors?

Benzyl Alcohol API manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Benzyl Alcohol API 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 Benzyl Alcohol API manufacturer or Benzyl Alcohol API supplier for your needs.

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

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

API | Excipient name

Benzyl Alcohol API

Synonyms

Phenylmethanol, Benzenemethanol, 100-51-6, Phenylcarbinol, Benzylalcohol, Benzoyl alcohol

Cas Number

100-51-6

Unique Ingredient Identifier (UNII)

LKG8494WBH

About Benzyl Alcohol API

A colorless liquid with a sharp burning taste and slight odor. It is used as a local anesthetic and to reduce pain associated with LIDOCAINE injection. Also, it is used in the manufacture of other benzyl compounds, as a pharmaceutic aid, and in perfumery and flavoring.

Tox21_300044 Manufacturers

A Tox21_300044 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300044, including repackagers and relabelers. The FDA regulates Tox21_300044 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300044 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Tox21_300044 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tox21_300044 Suppliers

A Tox21_300044 supplier is an individual or a company that provides Tox21_300044 active pharmaceutical ingredient (API) or Tox21_300044 finished formulations upon request. The Tox21_300044 suppliers may include Tox21_300044 API manufacturers, exporters, distributors and traders.

click here to find a list of Tox21_300044 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tox21_300044 USDMF

A Tox21_300044 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_300044 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_300044 DMFs exist exist since differing nations have different regulations, such as Tox21_300044 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Tox21_300044 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_300044 USDMF includes data on Tox21_300044's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_300044 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Tox21_300044 suppliers with USDMF on PharmaCompass.

Tox21_300044 CEP

A Tox21_300044 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300044 Certificate of Suitability (COS). The purpose of a Tox21_300044 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300044 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300044 to their clients by showing that a Tox21_300044 CEP has been issued for it. The manufacturer submits a Tox21_300044 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300044 CEP holder for the record. Additionally, the data presented in the Tox21_300044 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300044 DMF.

A Tox21_300044 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300044 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Tox21_300044 suppliers with CEP (COS) on PharmaCompass.

Tox21_300044 GMP

Tox21_300044 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_300044 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_300044 GMP manufacturer or Tox21_300044 GMP API supplier for your needs.

Tox21_300044 CoA

A Tox21_300044 CoA (Certificate of Analysis) is a formal document that attests to Tox21_300044's compliance with Tox21_300044 specifications and serves as a tool for batch-level quality control.

Tox21_300044 CoA mostly includes findings from lab analyses of a specific batch. For each Tox21_300044 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_300044 may be tested according to a variety of international standards, such as European Pharmacopoeia (Tox21_300044 EP), Tox21_300044 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tox21_300044 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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