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Manufactur standard N Acetyl Tyrosine Dosage - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex

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Manufactur standard N Acetyl Tyrosine Dosage - 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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Manufactur standard N Acetyl Tyrosine Dosage - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex detail pictures


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Often customer-oriented, and it's our ultimate target to become not only probably the most reputable, trustable and honest provider, but also the partner for our customers for Manufactur standard N Acetyl Tyrosine Dosage - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex , The product will supply to all over the world, such as: United States, Hungary, Costa rica, We've got constructed strong and long co-operation relationship with an enormous quantity of companies within this business in Kenya and overseas. Immediate and professional after-sale service supplied by our consultant group has happy our buyers. Thorough Info and parameters from the merchandise will probably be sent for you for any thorough acknowledge. Free samples may be delivered and company check out to our corporation. n Kenya for negotiation is constantly welcome. Hope to get inquiries type you and construct a long-term co-operation partnership.
  • 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 Bess from Zurich - 2018.12.11 14:13
    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 Lulu from South Korea - 2018.12.05 13:53
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