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Orlistat 99% Purity API for Lose-Weight Function Pharmaceutical Grade 96829-58-2
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- Product NameOrlistat 99% Purity API for Lose-Weight Function Pharmaceutical Grade 96829-58-2
- CAS No.96829-58-2
- Purity99%
- Min Quantity5000Kilograms
- Price1~1
- View Contact Detail
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Molecular Structure
Detailed Description
Orlistat 99% Purity API for Lose-Weight Function Pharmaceutical Grade 96829-58-2
Product Description
Orlistat 99% Purity API for Lose-Weight Function Pharmaceutical Grade for 10 Years Experience! ! 1Function
Orlistat is used with a low-calorie diet to help you lose weight and to maintain your weight after weight loss.
Orlistat is in a class of drugs called lipase inhibitors. It works in your intestines, where it blocks some of the fat you eat from being absorbed and digested. This undigested fat is then removed in your bowel movements
This is how a order arranged here :
1.Parcel would be arranged within 12 hours upon receipt of your payment .
Photos would be offered to tell apart the products . (send together steroids with real and original products )
Tracking number
2.Send by EMS, the tracking number is availabe within 12 hours . The info would be trackable that day or 1 day later.
3.If send by HKEMS or other express,the tracking number would be provided next day. And this does not mean the info is trackable that day. It would be released on internet 2 or 3 days later . The reason why is that parcel should be shipped to Hongkong from forwarder then wait for the flight .
4.You sign for the parcel , deliveried.
5.If you have any doubt about the products or parcel, please contact us immediately. Problem would be solved for the first time .
If there is anything you wanna know , pls feel free to contact :
1. Email : mxy01@ycphar.com
2. Skype ID : live:mxy01_1
3. Website : www.hqsteroid.com
I'm Sukie from China , serve you wholeheartedly.
Test Items Specifications
Appearance White or almost white crystalline powder
Specific Rotation -48° ~ -51.0°(on the anhydrous, solvent-free basis)
Identification A.HPLC: The retention time of the major peak of the sample solution corresponds to that of the standard solution.
B.IR: The IR spectrum of sample is consistent to the reference
Related Substances
Total impurity Not more than 1.0%
Related Compound A Not more than 0.2%
Related Compound B Not more than 0.05%
Related Compound C Not more than 0.05%
Related Compound D Not more than 0.2%
Related Compound E Not more than 0.2%
Formyl leucine Not more than 0.2%
Orlistat open ring epimer Not more than 0.2%
D-Leucine orlistat Not more than 0.2%
Orlistat open ring amide Not more than 0.1%
Individual unidentified impurity Not more than 0.1%
Residual Solvents
n-Hexane Not more than 5000ppm
Isopropyl ether Not more than 5000ppm
Residual on ignition Not more than 0.1%
Heavy Metal Not more than 20ppm
Water Not more than 0.2%
Assay 98.0%~101.5% (on the anhydrous, solvent-free basis)
Conclusion Conform with USP35 or EP
Certificate Of Analysis (COA)
Items Specification Items
Appearance white or almost white crystalline powder,smell less
Melting Point 42.0~46.0°C
Specific Rotation -31°~-39°(CHCl3,C=1)
Identification The result of HPLC is consisitent to the reference one. The result of IR is consisitent to the reference one.
Related Substances ≤ 0.5%
Total impurity ≤ 1.0%
Single impurity ≤ 0.1%
n-Hexane ≤ 290ppm
Isopropyl ether ≤ 5000ppm
Residual on Ignition ≤0.1%
Sulphate ≤ 0.05%
Heavy Metal ≤ 20ppm
Purity ≤ 99.0% ~ 99.9%
- Orlistat 99% Purity API for Lose-Weight Function Pharmaceutical Grade 96829-58-2