Residual Solvents Testing Services | PhytoVista Laboratories

We are not currently accepting residual solvent samples until further notice.

While manufacturers strive to remove all dangerous processing solvents, it is inevitable that small quantities will be left behind. At PhytoVista Laboratories, we use modern gas chromatography (GC) and flame ionization detection (HS-GC-FID) to measure headspace in residual solvents. We will analyse samples in our testing laboratory and provide you with a report stating whether the sample passed and if the concentrations of residential solvents are within EU regulations.

Residual Solvent Certificate of Analysis

Apply for your residual solvent lab testing certificate here.

Residual Solvents Analysis

Methanol

N-pentane

Ethanol

Diethyl ether

Acetone

Isopropanol

O-xylene

Dichloromethane

Chloroform

Cyclohexane

Hexane

Ethyl acetate

Benzene

1,2-dichloroethane

Heptane

Trichloroethane

Toluene

M-xylene

P-xylene

Analytical Request Form

Submit your product for testing using the analytical request form below

1 Customer Info

2 Test Info

3 Authorisation

Name
First Last
Company name to appear on certificate*
VAT No. (only applicable to EU companies)
Address*
Street Address Address Line 2 City County Post code Country
Customer email*
Customer phone*

Submit products for testing
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Special instructions
Authorisation*
Date*
Date Format: DD slash MM slash YYYY
By submitting products for Testing with PhytoVista, the customers agree that their samples fit the below criteria:
the preparation or other product is not designed for administration of the controlled drug to a human being or animal;*
- the preparation or other product is not designed for administration of the controlled drug to a human being or animal;
the controlled drug in any component part is packaged in such a form, or in combination with other active or inert substances in such a manner, that it cannot be recovered by readily applicable means or in a yield which constitutes a risk to health;*
- the controlled drug in any component part is packaged in such a form, or in combination with other active or inert substances in such a manner, that it cannot be recovered by readily applicable means or in a yield which constitutes a risk to health;
no one component part of the product or preparation contains more than one milligram of the controlled drug or one microgram in the case of lysergide or any other N-alkyl derivative of lysergamide*
- no one component part of the product or preparation contains more than one milligram of the controlled drug or one microgram in the case of lysergide or any other N-alkyl derivative of lysergamide
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