Leading Manufacturer for Furfuryl Acetate - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex
Leading Manufacturer for Furfuryl Acetate - 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:
Related Product Guide:
"Control the quality by the details, show the strength by quality". Our company has strived to establish a highly efficient and stable staff team and explored an effective quality control process for Leading Manufacturer for Furfuryl Acetate - 1-(4-METHOXYPHENYL)METHANAMINE – Gentolex , The product will supply to all over the world, such as: Bangalore, Jamaica, Afghanistan, Our Company policy is "quality first, to be better and stronger, sustainable development" . Our pursuit goals is "for society, customers, employees, partners and enterprises to seek reasonable benefit". We aspirate to do cooperate with all different the auto parts manufacturers, repair shop, auto peer , then create a beautiful future! Thank you for taking time to browse our website and we would welcome any suggestions you may have that can help us to improve our site.
By trameka milhouse from Canberra - 2017.12.19 11:10
The goods we received and the sample sales staff display to us have the same quality, it is really a creditable manufacturer.
By Maxine from Porto - 2018.05.15 10:52
