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Newly Arrival Mometasone Furoate - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex

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With a positive and progressive attitude to customer's interest, our company continuously improves our product quality to meet the needs of customers and further focuses on safety, reliability, environmental requirements, and innovation of Cetylpyridinium Chloride, Vinyl Acetate, Duloxetine Hcl, Our team members are aim to provides products with high performance cost ratio to our customers, and the goal for all of us is to satisfy our consumers from all over the world.
Newly Arrival Mometasone Furoate - 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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Newly Arrival Mometasone Furoate - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex detail pictures


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  • We are long-term partners, there is no disappointment every time, we hope to maintain this friendship later!
    5 Stars By Ellen from Ireland - 2018.03.03 13:09
    The factory has advanced equipment, experienced staffs and good management level, so product quality had assurance, this cooperation is very relaxed and happy!
    5 Stars By Denise from Orlando - 2018.02.12 14:52
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