In-source chemical modification of non polar analytes using atmospheric pressure chemical ionisation source

Patent metadata

Field	Value
Publication number	US-10049866-B2
Application number	US-201715487537-A
Country	US
Kind code	B2
Filing date	Apr 14, 2017
Priority date	Apr 15, 2016
Publication date	Aug 14, 2018
Grant date	Aug 14, 2018

Abstract

A method for analyzing an aliphatic compound by mass spectrometry which comprises: (i) ionizing an aliphatic compound in the presence of a heterocyclic modifier; and (ii) mass analyzing the resulting ions to obtain mass spectrometric data.

First claim

The invention claimed is:

1. A method of mass spectral analysis of an aliphatic compound, comprising: ionizing the aliphatic compound in the presence of a heterocyclic compound.

2. The method of claim 1 , wherein the ionisation process is atmospheric pressure chemical ionisation (APCI), atmospheric pressure photoionisation (APPI), or APCI/APPI mixed mode ionisation.

3. The method of claim 1 , wherein the mass spectral analysis utilises GC-MS, LC-MS or SFC-MS.

4. A method of atmospheric pressure chemical ionisation mass spectrometry for gas chromatography (APCI-GC) of an aliphatic compound, comprising: performing the APCI-GC of the aliphatic compound in the presence of a heterocyclic compound.

5. A method for analysing an aliphatic compound by mass spectrometry which comprises:
(i) ionising an aliphatic compound in the presence of a heterocyclic modifier; and
(ii) mass analysing the resulting ions to obtain mass spectrometric data.

6. A method according to claim 5 , wherein the ionisation is atmospheric pressure chemical ionisation, atmospheric pressure photoionisation or atmospheric pressure chemical ionisation/atmospheric pressure photoionisation mixed mode ionisation.

7. A method according to claim 5 , further comprising subjecting the ions resulting from step (i) to ion mobility separation prior to mass analysing them.

8. A method according to claim 5 , wherein the mass spectrometric data is compared with mass spectrometric data obtained without use of the heterocyclic modifier and/or with mass spectrometric data obtained using a different heterocyclic modifier.

9. A method according to claim 5 , wherein the mass spectrometry is tandem mass spectrometry.

10. A method according to claim 5 , wherein prior to ionisation the aliphatic compound is in effluent from a gas-chromatograph.

11. A method according to claim 5 wherein prior to ionisation the aliphatic compound is in effluent from a liquid-chromatograph.

12. A method according to claim 5 wherein prior to ionisation the aliphatic compound is in effluent from a supercritical fluid chromatograph.

13. A method according to claim 5 wherein the mass spectrometry is atmospheric pressure chemical ionisation mass spectrometry for gas chromatography.

14. A method according to claim 5 wherein the aliphatic compound is a linear or branched chain hydrocarbon.

15. A method according to claim 5 wherein the aliphatic compound is an alkane, alkene or alkyne, or a mixture thereof.

16. A method according to claim 5 wherein the aliphatic compound is a hydrocarbon containing 5 or more carbon atoms.

17. A method according to claim 5 wherein the aliphatic compound is a C 5 to C 120 hydrocarbon.

18. A method according to claim 5 wherein the aliphatic compound is comprised in crude oil or a fraction thereof.

19. A method according claim 5 wherein the heterocyclic modifier is a mono-, bi- or tricyclic heterocyclic compound containing carbon atoms and 1-4 heteroatoms.

20. A method according to claim 19 , wherein the heteroatoms are selected from oxygen, sulphur and/or nitrogen.

21. A method according to claim 5 wherein the heterocyclic modifier is monocyclic.

22. A method according to claim 5 wherein the heterocyclic modifier is aromatic.

23. A method according to claim 5 wherein the heterocyclic modifier is selected from oxetane, azetidine, thietane, pyrrole, furan, tetrahydrofuran, thiophene, tetrahydrothiophene (thiolane, thiophane), indole, benzothiophene, benzofuran (coumarone), dioxane, piperazine, thiane, dithiane, pyrrolidine, pyridine, pyrimidine, pyrazine, pyran, thiopyran, piperadine, tetrahydropyran, imidazoline, imidazole, pyrazole, oxazole, thiazole, isoxazole, triazole, tetrazole, quinoline, isoquinoline, purine, dibenzofuran and dibenzothiophene, and alkylated derivatives thereof.

24. A method according to claim 5 wherein the heterocyclic modifier is pyrrole.

Assignees

• Micromass Ltd

Inventors

• Douce David
• Jones Gareth R

Classifications

• H01J49/0045

  characterised by the fragmentation or other specific reaction · CPC title

• H01J49/0031

  Step by step routines describing the use of the apparatus (H01J49/0081 takes precedence) · CPC title

• G01N30/7206

  interfaced to gas chromatograph (interfaces in general for introducing or extracting samples to be analysed with specially adapted mass spectrometer, see H01J49/04) · CPC title

• G01N30/72

  Mass spectrometers {(mass spectrometers per se H01J49/00)} · CPC title

• H01J49/145 Primary

  using chemical ionisation · CPC title