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Manufactur standard Coenzyme Q10 - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex

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Having a sound small business credit score, outstanding after-sales services and modern manufacturing facilities, we've got earned an fantastic reputation among our buyers across the globe for 3-Bromopropylamine Hydrobromide, 4-Methoxyphenylacetone, Sodium Chloride, Our products are new and old customers consistent recognition and trust. We welcome new and old customers to contact us for future business relations, common development. Let's speeding in the dark!
Manufactur standard Coenzyme Q10 - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex Detail:

Product Detail

CasNo 2393-23-9 DeliveryTime within 10 days
Molecular C8H11NO Production Capacity 1 Metric Ton/Day
Appearance Clear,colorless to slightly yellow liquid Purity 99%min
Application Pharmaceutical intermediates Storage Room temperature, dark, sealed
LimitNum 1 Kilogram Transportation Air, Sea, Express.
Density 1.05g/mLat25°C(lit.) Boiling Point 236-237°C(lit.)
Melting Ponit -10°C Refractive index n20/D1.546(lit.)
Flash Point: >230°F Solubility Highly soluble in water
Name p-anisylamine or (4-methoxyphenyl)methanamine    

Synonyms

 LABOTEST-BB LTBB000703; AKOS BBS-00003589; 4-AMINOMETHYL-ANISOLE; 4-METHOXYBENZYLAMINE; P-Methoxybenzylamine Hydrochloride173.64; 4-Methoxybenzylamine, 98+%; for Sparfloxacine; P-METHOXYBENZYLAMINE HYDROCHLORIDE

Application

It can be used for the synthesis of pharmaceutical intermediates. It is slightly harmful to water. Do not let undiluted or large quantities of products come into contact with groundwater, waterways or sewage systems. Without government permission, do not discharge materials into the surrounding environment to avoid oxides, acids. , air, carbon dioxide contact, keep the container sealed, put it in a tight extractor, and store in a cool, dry place.

QC Lab

An individual QC laboratory stands in the site where chemical, physical test, microbial test, stability study, instrument test such as IR, UV, HPLC, GC are performed for raw materials and finished products. The whole area is access controlled and well maintained with sufficient analytical instruments for intended testing purpose. All instruments are well labelled and appropriately calibrated.

QA

QA is responsible to evaluate and categorize the deviation into Major level, General level and Minor level. For all levels of deviations, the investigation to identify the root cause or potential cause is necessary. Investigation needs to be completed within 7 working days. The product impact assessment along with CAPA plan are also required after the investigation complete and root cause identified. The deviation is closed when the CAPA is implemented. All Level deviation should be approved by QA Manager. After implemented, effectiveness of CAPA is confirmed based on plan.


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We depend on sturdy technical force and continually create sophisticated technologies to meet the demand of Manufactur standard Coenzyme Q10 - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex , The product will supply to all over the world, such as: Belgium, kazan, San Diego, Upon today, we have customers from all over the world, including USA, Russia, Spain, Italy, Singapore, Malaysia, Thailand, Poland, Iran and Iraq. The mission of our company is to provide the highest quality products with best price. We are looking forward to doing business with you!
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