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Hydroxyethyl cellulose
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Producer
Produced in:
Established in: 1886
MOQ: 5 kg
Employees: 275+
Raw materials, CMO and OTC products
Two GMP certified locations
Customisable (small-sized) packages
+ 0
All certificates
Distributor
Produced in:
Established in: 2019
MOQ: -
Employees: 50+
ISO 9001, SGS, Certificated supplier.
Audit available either on site or remote.
Professional One Stop Service for delivery to customers.
+ 0
All certificates
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Looking for Hydroxyethyl cellulose API 9004-62-0?
- Description:
- Here you will find a list of producers, manufacturers and distributors of Hydroxyethyl cellulose. You can filter on certificates such as GMP, FDA, CEP, Written Confirmation and more. Send inquiries for free and get in direct contact with the supplier of your choice.
- API | Excipient name:
- Hydroxyethyl cellulose
- Synonyms:
- Cellulose hydroxyethyl ether , Cellulose hydroxyethylate , hydroxyethylcellulose
- Cas Number:
- 9004-62-0
- DrugBank number:
- DB11602
- Unique Ingredient Identifier:
- X70SE62ZAR
About Hydroxyethyl cellulose
It's time for some technical information for the ones who understand chemistry: Hydroxyethyl cellulose is a polysaccharide derivative with gel thickening, emulsifying, bubble-forming, water-retaining and stabilizing properties. It is used as a key ingredient in many household cleaning products, lubricants and cosmetics due to its non-ionic and water-soluble nature. It is often used as an ingredient in ophthalmic pharmaceutical preparations such as artificial tear solutions and adjunct agent in topical drug formulations to facilitate the delivery of drugs with hydrophobic character.
You can ask the supplier for more technical information about the product.
Hydroxyethyl cellulose is a type of Hypromellose
Hypromellose, also known as hydroxypropyl methylcellulose (HPMC), is a widely used pharmaceutical active pharmaceutical ingredient (API) belonging to the subcategory of pharmaceutical excipients. It is a non-ionic cellulose ether derived from natural polymer cellulose, making it a safe and biocompatible compound for pharmaceutical applications.
Hypromellose is primarily utilized in the pharmaceutical industry as a thickening agent, binder, film former, and sustained-release matrix material. It is commonly employed in the formulation of oral solid dosage forms such as tablets and capsules. Due to its hydrophilic nature, hypromellose aids in enhancing the dissolution rate and bioavailability of poorly soluble drugs.
One of the key advantages of hypromellose is its ability to modify the drug release profile. By adjusting the viscosity and concentration of hypromellose in the formulation, pharmaceutical manufacturers can achieve controlled and extended drug release, ensuring optimal therapeutic efficacy and patient compliance. This makes hypromellose a preferred choice for the development of sustained-release and controlled-release dosage forms.
In addition, hypromellose offers excellent film-forming properties, making it suitable for coating tablets to improve their appearance, protect the active ingredient from degradation, and facilitate ease of swallowing. It also acts as a binder, imparting cohesive properties to powdered drug formulations, allowing for the production of compressed tablets with adequate hardness and mechanical strength.
Overall, hypromellose is a versatile and valuable API subcategory in the pharmaceutical industry, providing numerous benefits such as enhanced drug solubility, controlled release, and improved formulation characteristics for various oral dosage forms.
Hydroxyethyl cellulose (Hypromellose), classified under Additives
Additives in the pharmaceutical API category refer to a group of chemical substances that are incorporated into pharmaceutical products to enhance their stability, functionality, or performance. These additives play a crucial role in ensuring the quality, safety, and efficacy of medications.
One common type of additive used in pharmaceuticals is preservatives. Preservatives are added to prevent microbial growth and maintain the integrity of the product throughout its shelf life. They help to safeguard against contamination and maintain the potency of the active pharmaceutical ingredient (API). Some commonly used preservatives include benzyl alcohol, phenol, and parabens.
Another important group of additives is antioxidants. Antioxidants are added to pharmaceutical formulations to prevent or delay the oxidation of APIs, which can lead to degradation and loss of potency. Examples of antioxidants commonly used in pharmaceuticals include ascorbic acid (vitamin C) and tocopherols (vitamin E).
In addition to preservatives and antioxidants, other additives like flavorings, colorants, and sweeteners may be incorporated into pharmaceutical products to improve their palatability and patient acceptability.
It is crucial to note that the use of additives in pharmaceuticals is strictly regulated by health authorities to ensure their safety and efficacy. Manufacturers must comply with stringent quality control standards and guidelines to guarantee the proper use and appropriate levels of additives in pharmaceutical products.
Overall, additives play a vital role in the pharmaceutical industry by enhancing the stability, functionality, and patient acceptability of medications. Their careful selection and incorporation contribute to the overall quality and effectiveness of pharmaceutical products.
Hydroxyethyl cellulose manufacturers | traders | suppliers
We have 2 companies offering Hydroxyethyl cellulose produced in 2 different countries.
Get in contact with the supplier of your choice:
- Caesar & Loretz GmbH (CAELO) from Germany, product country of origin Netherlands
- Aurora Industry Co., Ltd from China, product country of origin China
Let the supplier know whether you are looking for a product with a specific monograph such as EP (Ph. Eur.), USP, JP, BP or another quality. Or, whether you are looking for hydrochloride (HCl), anhydricum, base, micronisatum or a specific purity.
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