Low price for Pseudouridine - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex
Low price for Pseudouridine - 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.
Product detail pictures:
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Our company since its inception, always regards product quality as enterprise life, continuously improve production technology, improve product quality and continuously strengthen enterprise total quality management, in strict accordance with the national standard ISO 9001:2000 for Low price for Pseudouridine - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex , The product will supply to all over the world, such as: Montreal, Mexico, Costa rica, By integrating manufacturing with foreign trade sectors, we can provide total customer solutions by guaranteeing the delivery of right products to the right place at the right time, which is supported by our abundant experiences, powerful production capability, consistent quality, diversified products and the control of the industry trend as well as our maturity before and after sales services. We'd like to share our ideas with you and welcome your comments and questions.
By Tina from Italy - 2017.12.09 14:01
This company conforms to the market requirement and joins in the market competition by its high quality product, this is an enterprise that have Chinese spirit.
By Joanne from Monaco - 2018.02.21 12:14
