HPLC

Troubleshooting
Guide

CALL PHENOMENEX FOR:

n HPLC

Columns (capillary to preparative)

SEC Columns: Aqueous (GFC) and non-Aqueous (GPC)
n Amino Acid Analysis
n HPLC Specialty Columns for Analysis of:
n Basic, acidic and amphoteric drugs

n High/Low pH separations (pH 1-12)

n Proteins/Peptides by reversed phase

n Biopolymers - Proteins and Nucleic Acids by GFC/SEC

n Synthetic polymers

n Foods and Beverages

n Environmental Samples

n Drugs in biological fluids

n HPLC Bulk Media
n HPLC Accessories such as:
n Sample and Solvent Filters

n SecurityGuard Column Protection

n Syringe Filters

n Syringes and Vials

n Column Heater / Column Chiller-Heater

n HPLC Injection Valves

n Tubings and Fittings

n Solvent Degassers

n Column Selectors

n Fluid Processors

n GC Columns
n SPE Tubes and 96-Well plates
n

n Application

Development and Validation Support

Technical Service

n Outstanding

TABLE OF CONTENTS

I.

Introduction....................................................................................... 1

II.

Abnormal Pressure........................................................................... 2

III.

Leaks................................................................................................ 4

IV.

Problems with the Chromatogram.................................................... 6

V.

Problems with the Injector.............................................................. 14

VI.

Problems Detected by Smell, Sight, or Sound............................... 15

VII.

Key Problem Areas and Preventive Maintenance........................... 17

SecurityGuard Universal HPLC Guard Cartridge System.............. 19

Phenex Syringe Filters.................................................................... 20

2008 Phenomenex, Inc. All rights reserved.

No part of this booklet may be copied without prior written permission from Phenomenex, Inc. USA.
While every attempt has been made to ensure the accuracy of the information contained in this
guide, Phenomenex assumes no responsibility for its use. We welcome any additions or corrections
for incorporation into future editions.

I. Introduction
LOCATING AND CORRECTING THE PROBLEM
A systematic approach to identifying the problem is the best approach to troubleshooting your HPLC system. This guide is organized by five major categories
of symptoms to help you quickly identify the source of the problem(s) you are
encountering:

pressure abnormalities

leaks

problems with the chromatogram

injector problems

other problems detected by the senses of smell, sight, and sound
When you have corrected the problem, record the incident in the system recordbook to help with future problems.
PREVENTION
Many LC problems can be prevented with routine preventive maintenance. For
example, replacing pump seals at regular intervals should eliminate pump-seal
failure and its associated problems. Section VII lists the most common problem
areas for each LC module, and preventive maintenance practices that will reduce their frequency. These suggestions should be modified to fit your particular
model of LC, and then made a regular part of your laboratory routine.
WHERE TO GET ADDITIONAL HELP
The operators and service manuals for the instrument should be consulted.
These contain exploded diagrams, troubleshooting procedures for specific
models, and part numbers to help you order replacement parts.
Other people in the lab may have had experience solving a problem which is
giving you trouble; they can be a helpful resource.
The manufacturer of your instrument can help you. Most LC manufacturers
offer free technical support to their customers.
Phenomenex has experienced technical consultants who can assist you with
almost any problem. We welcome your phone calls, faxes or emails.
Phenomenex offers seminars, as well as a complete line of reference books
on HPLC.
There are a number of reference sources that can give you guidance
in problem solving:
J.W. Dolan and L.R. Snyder, Troubleshooting LC Systems, Humana Press, NJ
(1989). Phenomenex Order No.: AA0-1717
L.R. Snyder and J.J. Kirkland, Introduction to Modern Liquid Chromatography,
2nd ed., Wiley, NY (1979). Phenomenex Order No.: AA0-1700
D.J. Runser, Maintaining and Troubleshooting HPLC Systems - A Users
Guide, Wiley, NY (1981).
J.W. Dolan, Troubleshooting, LC/GC Magazine. This is a monthly column.

II. Abnormal Pressure

A change in the operating pressure is a sign that there may be a problem.
Choose the category below that best fits the symptoms that you observe, and
follow the suggestions to correct the problem.

A. No pressure reading, no flow

POSSIBLE CAUSE

SOLUTION

1. Power off

1. Turn on power

2. Fuse blown

2. Replace fuse

3. Controller setting or failure

3. a. Verify proper settings
b. Repair or replace controller
4. Broken piston

4. Replace piston

5. Air trapped in pump head

5. Degas solvents; bleed air
from pump, prime pump
6. Insufficient mobile phase
6. a. Replenish reservoir
b. Replace inlet frit if blocked
7. Faulty check valve(s)

7. Replace check valve(s)

8. Major leak

8. Tighten or replace fittings

B. No pressure reading, flow is normal

POSSIBLE CAUSE

SOLUTION

1. Faulty meter

1. Replace meter

2. Faulty pressure transducer

2. Replace transducer

C. Steady, high pressure

POSSIBLE CAUSE

SOLUTION

1. Flow rate set too high

1. Adjust setting

2. Blocked column frit

2. a. Backflush column (if permitted)
b. Replace frit*

c. Replace column
3. Improper mobile phase;
3. a. Use correct mobile phase
precipitated buffer b. Wash column
4. Improper column

4. Use proper column

5. Injector blockage

5. Clear blockage or replace injector

6. Column temperature too low

6. Raise temperature

7. Controller malfunction

7. Repair or replace controller

8. Blocked guard column

8. Remove/replace guard column

9. Blocked in-line filter

9. Remove/replace in-line filter

* Check manufacturers column warranty first. Removal of end-fittings may void column warranty.

II. Abnormal Pressure (continued)

D. Steady, low pressure
POSSIBLE CAUSE

SOLUTION

1. Flow set too low

1. Adjust flow rate

2. Leak in system

2. Locate and correct

3. Improper column

3. Use proper column

4. Column temperature too high

4. Lower temperature

5. Controller malfunction

5. Repair or replace controller

E. Pressure climbing
POSSIBLE CAUSE

SOLUTION

1. See section C

1. See section C

F. Pressure dropping to zero

POSSIBLE CAUSE

SOLUTION

1. See sections A and B

1. See sections A and B

G. Pressure dropping, but not to zero

POSSIBLE CAUSE

SOLUTION

1. See section D

1. See section D

H. Pressure cycling
POSSIBLE CAUSE

SOLUTION

1. Air in pump
1. a. Degas solvent
b. Bleed air from pump
2. Faulty check valve(s)

2. Replace check valve(s)

3. Pump seal failure

3. Replace pump seal

4. Insufficient degassing
4 a. Degas solvent
b. Change degassing methods
(use Degassex on-line degasser)
5. Leak in system

5. Locate and correct

6. Using gradient elution

6. Pressure cycling is normal due to
viscosity changes

III. Leaks
Leaks are usually stopped by tightening or replacing a fitting. Be aware, however, that overtightened metal compression fittings can leak and plastic fingertights
can wear out. If a fitting leak does not stop when the fitting is tightened a little,
take the fitting apart and inspect for damage (e.g. distorted ferrule, or particles
on the sealing surface); damaged fittings should be discarded.

A. Leaky fittings
possible cause solution

1. Loose fitting

1. Tighten

2. Stripped fitting

2. Replace

3. Overtightened* fitting
3. a. Loosen and retighten
b. Replace
4. Dirty fitting
4. a. Disassemble and clean
b. Replace
5. Mismatched parts

5. Use all parts from same brand

B. Leaks at pump
possible cause solution

1. Loose check valves

1. a. Tighten check valve
(do not overtighten)
b. Replace check valve
2. Loose fittings

2. Tighten fittings (do not overtighten)

3. Mixer seal failure

3. a. Replace mixer seal
b. Replace mixer
4. Pump seal failure

4. Repair or replace

5. Pressure transducer failure

5. Repair or replace

6. Pulse damper failure

6. Replace pulse damper

7. Proportioning valve failure

7. a. Check diaphragms,
replace if leaky
b. Check for fitting damage,
replace
8. Purge valve
8. a. Tighten valve
b. Replace purge valve

* Use fingertight end-fittings to avoid sealing problems and the need for wrenches

III. Leaks (continued)

C. Injector leaks
possible cause solution

1. Rotor seal failure

1. Rebuild or replace injector

2. Blocked loop

2. Replace loop

3. Loose injection-port seal

3. Adjust

4. Improper syringe-needle diameter 4. Use correct syringe

5. Waste-line siphoning
5. Keep waste line
above surface waste
6. Waste-line blockage

6. Replace waste line

D. Column leaks
possible cause solution

1. Loose endfitting

1. Tighten endfitting

2. Column packing in ferrule

2. Disassemble, rinse ferrule,
reassemble
3. Improper frit thickness

3. Use proper frit (see chart below)

E. Detector leaks
possible cause solution

1. Cell gasket failure

1. a. Prevent excessive backpressure
b. Replace gasket
2. Cracked cell window(s)

2. Replace window(s)

3. Leaky fittings

3. Tighten or replace

4. Blocked waste line

4. Replace waste line

5. Blocked flow cell

5. Rebuild or replace

frit Pore Size selection guide

Frit Pore Size should be:

When Particle Size of

material is:

0.5 m

3 - 4 m

2 m

5 - 20 m

IV. Problems with the Chromatogram

Many problems in the LC system show up as changes in the chromatogram.
Some of these can be solved by changes in the equipment; however, others
require modification of the assay procedure. Selecting the proper column type
and mobile phase are keys to good chromatography.

A. Peak tailing
possible cause solution

1. Blocked frit
1. a. Reverse fIush column (if allowed)
b. Replace inlet frit*
c. Replace column
2. Column void

2. Fill void

3. Interfering peak
3. a. Use longer column
b. Change mobile phase
and/or column/selectivity
4. Wrong mobile phase pH.
4. Adjust pH. For basic compounds,
lower pH usually provides more
symmetric peaks
5. Sample reacting with active sites. 5. a. Add ion pair reagent or volatile
basic modifier
b. Change column
Normal
Problem

PEAK TAILING

B. Peak fronting
possible cause solution

1. Low temperature

1. Increase column temperature

2. Wrong sample solvent

2. Use mobile phase for
injection solvent
3. Sample overload

3. Decrease sample concentration

4. Bad column

4. See A.1. and A.2.

C. Split peaks
possible cause solution

1. Contamination on guard or
1. Remove guard column and
analytical column inlet. attempt analysis. Replace guard
continued on next page
* Check manufacturers column warranty first. Removal of end-fittings may void column warranty.

IV. Problems with the Chromatogram (continued)

C. Split peaks (continued)
possible cause solution

if necessary. If analytical column

is obstructed, reverse and flush. If

problem persists, column may
Normal
Problem

be fouled with strongly retained

contaminants. Use appropriate

restoration procedure. If problem

persists, inlet is probably plugged.

Change frit or replace column
SPLIT PEAKS

2. Sample solvent incompatible with 2. Change solvent. Whenever possible,
mobile phase. inject samples in mobile phase

D. Distortion of larger peaks

POSSIBLE CAUSE solution

1. Sample overload

1. Reduce sample size

E. Distortion of early peaks

POSSIBLE CAUSE solution

1. Wrong injection solvent

1. a. Reduce injection volume
b. Use weaker injection solvent

F. Tailing, early peaks more than later ones

POSSIBLE CAUSE solution

1. Extra-column effects
1. a. Replumb system
(shorter, narrower tubing)
b. Use smaller volume detector cell

G. Increased tailing as k increases

POSSIBLE CAUSE solution

1. Secondaryretention effects,
1.
reversed-phase mode

a. Add triethylamine (basic samples)

b. Add acetate (acidic samples).
c. Add salt or buffer (ionic samples)
d. Try a different column.
e. See page 19

2. Secondaryretention effects,
2. a. Add triethylamine
normal-phase mode (basic compounds)
b. Add acetic acid
(acidic compounds)

IV. Problems with the Chromatogram (continued)

G. Increased tailing as k increases (continued)
POSSIBLE CAUSE solution

2. Secondaryretention effects,
2. c. Add water
normal-phase mode (poly-functional compounds).
Only for normal-phase methods
which use water-miscible solvents.
d. Try a different LC method
3. Secondaryretention effects, ion-pair 3. Add triethylamine (basic samples)

H. Acidic or basic peaks tail

POSSIBLE CAUSE solution

1. Inadequate buffering
1. a. Use 50-100 mM buffer
concentration
b. Use buffer with pKa equal
to pH of mobile phase
c. See page 19

I. Extra peaks
POSSIBLE CAUSE solution

1. Other components in sample

1. Normal

2. Late-eluting peak from

2. a. Increase run time
previous injection or gradient slope
b. Increase flow rate
3. Vacancy or ghost peaks
3. a. Check purity of mobile phase
b. Use mobile phase as
injection solvent
c. Reduce injection volume
4. Contamination

4. Filter sample

J. Retention time drifts

POSSIBLE CAUSE solution

1. Poor temperature control

1. Thermostat column

2. Mobile phase changing

2. Prevent change
(evaporation, reaction, etc.)
3. Poor column equilibration
3. Allow more time for column
equilibration between runs

K. Abrupt retention time changes

POSSIBLE CAUSE solution

1. Flow rate change

1. Reset flowrate

2. Air bubble in pump

2. Bleed air from pump

3. Improper mobile phase

3. a. Replace with proper
mobile phase
b. Set proper mobile phase
mixture on controller

IV. Problems with the Chromatogram (continued)

L. Baseline drift
POSSIBLE CAUSE solution

1.

Column temperature fluctuation.

1. Control column and mobile phase
(Even small changes cause cyclic temperature, use heat exchanger
baseline rise and fall. Most often before detector
affects refractive index and
conductivity detectors, or UV
Normal
Problem
detectors at high sensitivity or in
BASELINE DRIFT
direct photometric mode.)

2.

Nonhomogenous mobile phase.

2.
(Drift usually to higher absorbance,
rather than cyclic pattern from

temperature fluctuation.)

Use HPLC grade solvents, high

purity salts, and additives. Degas
mobile phase before use, sparge
with helium during use.

3. Contaminant or air buildup in

3.
detector cell

Flush cell with methanol or other

strong solvent. If necessary,
clean cell with 1N HNO3 (never
with HCI.)

4. Plugged outlet line after detector. 4. Unplug or replace line. Refer

(High pressure cracks cell window, to detector manual to replace
producing noisy baseline.) window.
5. Mobile phase mixing problem or 5. Correct composition / flow rate.
change in flow rate To avoid, routinely monitor
composition and flow rate
6. Slow column equililbration,
6.
especially when changing
mobile phase

Flush with intermediate strength

solvent, run 10-20 column
volumes of new mobile phase
before analysis

7. Mobile phase contaminated,

7. Check make-up of mobile phase.
deteriorated, or prepared from Use highest grade chemicals and
low quality materials HPLC solvents
8.

Strongly retained materials in

8.
sample (high k) can elute as
very broad peaks and appear
to be a rising baseline. (Gradient
analyses canaggravate problem.)

Use guard column. If necessary,

flush column with strong solvent
between injections or periodically
during analysis.

9. Mobile phase recycled but

9. Reset baseline. Use new mobile
detector not adjusted phase when dynamic range of
detector is exceeded.
10. Detector (UV) not set at
10. Change wavelength to
absorbance maximum but at UV absorbance maximum
slope of curve

IV. Problems with the Chromatogram (continued)

M. Baseline noise (regular)
POSSIBLE CAUSE solution

1. Air in mobile phase, detector cell, 1. Degas mobile phase. Flush

or pump system to remove air from
detector cell or pump
2. Leak
2.
Normal


Problem

BASELINE NOISE

3. Incomplete mobile phase mixing
less viscous solvent

See section Ill. Check system for

loose fittings. Check pump for
leaks, salt build-up, unusual
noises. Change pump seals if
necessary

3. Mix mobile phase by hand or use

4. Temperature effect (column at high 4. Reduce differential or add heat

temperature, detector unheated) exchanger
5. Other electronic equipment on
5. Isolate LC, detector or recorder to
same line determine if source of problem is
external. Correct as neccessary
6. Pump pulsations
6. Incorporate pulse dampener into
system

N. Baseline noise (irregular)

POSSIBLE CAUSE solution

1. Leak
1.
Normal


Problem


BASELINE NOISE

See section III. Check for loose

fittings. Check pump for leaks,
salt build-up, unusual noises.
Change seals if neccessary.
Check for detector cell leak

2. Mobile phase contaminated,

2. Check make-up of mobile phase.
deteriorated, or prepared from low
quality materials
3. Mobile phase solvents immiscible 3. Select and use only miscible
solvents
4. Detector/recorder electronics
4. Isolate detector and recorder
electronically. Refer to instruction
manual to correct problem
5. Air trapped in system

5. Flush system with strong solvent

6. Air bubbles in detector

6. Purge detector. Install back-
pressure device after detector

continued on next page

10

IV. Problems with the Chromatogram (continued)

N. Baseline noise (irregular) continued
POSSIBLE CAUSE solution

7. Detector cell contaminated (even 7. Clean cell by flushing with

small amounts of contaminants 1N HNO3 (never with HCI)
can cause noise)
8. Weak detector lamp

8. Replace lamp

9. Column leaking silica

or packing material

9. Replace column

10. Mobil phase mixer inadequate

10. Repair or replace the mixer
or malfunctioning or mix off-line if isocratic

O. Broad peaks
POSSIBLE CAUSE solution

1. Mobile phase composition changed 1. Prepare new mobile phase

2. Mobile phase flow rate too low

2. Adjust flow rate

3. Leaks (especially between column 3.

and detector)


4. Detector settings incorrect

See section III. Check for loose

fittings. Check pump for leaks,
salt build-up, and unusual noises.
Change seals if necessary

4. Adjust settings

5. Extra-column effects:
5. a. Inject smaller volume (e.g.,
a. Column overloaded 10 L vs. 100 L) or 1:10 and
1:100 dilutions of sample
b. Detector response time or cell b. Reduce response time or use
volume too large smaller cell
c. Tubing between column and c. Use as short a piece of 0.007-
detector too long or ID too large 0.010 in. ID tubing as practical
d. Recorder response time too high d. Reduce response time

Normal

Problem

BROAD PEAKS

11

IV. Problems with the Chromatogram (continued)

O. Broad peaks (continued)
POSSIBLE CAUSE solution

6. Buffer concentration too low

6. Increase concentration

7. Guard column

contaminated/worn out

7. Replace guard column

8. Column contaminated / worn out. 8. Replace column with new one

Low plate number of same type
9. Void at column inlet
9. Open inlet end and fill void
or replace column
10. Peak represents two or more poorly 10. Change column type to improve
resolved compounds separation
11. Column temperature too low
11. Increase temperature. Do
not exceed 60 C unless higher
temperatures are acceptable
to column manufacturer
12. Detector time constant too large

12. Use smaller time constant

P. Loss of resolution
POSSIBLE CAUSE solution

1. Mobile phase contaminated /

1. Prepare new mobile phase
deteriorated (causing retention
time to change)
2. Obstructed guard or
2.
analytical column








Normal

Problem
LOSS OF RESOLUTION

12

Remove guard column and

attempt analysis. Replace guard
if necessary. If analytical column
is obstructed, reverse and flush.
If problem persists, column may
be fouled with strongly retained
contaminants. Use appropriate
restoration procedure. If problem
persists, inlet is probably plugged.
Change frit or replace column.

IV. Problems with the Chromatogram (continued)

Q. All peaks too small
POSSIBLE CAUSE solution

1. Detector attenuation too high

1. Reduce attenuation

2. Detector time constant too large

2. Use smaller time constant

3. Injection size too small

3. a. Increase sample concentration
b. Increase injection volume, if
column size allows
4. Improper recorder connection

4. Use correct connection

R. All peaks too large

POSSIBLE CAUSE solution

1. Detector attenuation too low

1. Use larger attenuation

2. Injection size too large

2. a. Reduce sample concentration
b. Decrease injection volume, use
a smaller sample loop or use
partial loop filling
3. Improper recorder connection

3. Use correct connection

13

V. Problems with the injector

These problems are usually detected while you are using the injection valve.
Leaky injection valves are discussed in Section III (Leaks).

A. Manual injector, hard to turn

POSSIBLE CAUSE solution

1. Damaged rotor seal

1. Rebuild or replace valve

2. Rotor too tight

2. Adjust rotor tension

B. Manual injector, hard to load

POSSIBLE CAUSE solution

1. Valve misaligned

1. Adjust alignment.

2. Blocked loop

2. Replace loop

3. Dirty syringe

3. Clean or replace syringe

4. Blocked lines

4. Clear or replace lines

C. Autoinjector, wont turn

POSSIBLE CAUSE solution

1. No air pressure (or power)

1. Supply proper pressure (power)

2. Rotor too tight

2. Adjust

3. Valve misaligned

3. Adjust alignment

D. Autoinjector, other problems

POSSIBLE CAUSE solution

1. Blockage

1. Clear or replace blocked portion

2. Jammed mechanism

2. See service manual

3. Faulty controller

3. Repair or replace controller

14

VI. Problems Detected by SMELL, SIGHT OR SOUND

You need to use all your senses to identify LC problems. You should get in the
habit of taking a few minutes each day to expose all of your senses (except
taste!) to the LC so that you can get a feel for how the LC performs normally.
This will help you to quickly locate problems. For example, often you can smell
a leak before you see it. The majority of problems are identified by sight; most
of these are included in the preceeding section.

A. Solvent smell
POSSIBLE CAUSE solution

1. Leak

1. See section III

2. Spill
2. a. Check for overflowing waste
container
b. Locate spill and clean up

B. Hot smell
POSSIBLE CAUSE solution

1. Overheating module
1. a. Check for proper ventilation,
adjust
b. Check temperature setting,
adjust
c. Shut module off, see service
manual

C. Abnormal meter readings

POSSIBLE CAUSE solution

1. Pressure abnormality

1. See section II

2. Column oven problem

2. a. Check settings, adjust
b. See service manual
3. Detector lamp failing

3. Replace lamp

D. Warning lamps
POSSIBLE CAUSE solution

1. Pressure limit exceeded

1. a. Check for blockage
b. Check limit setting, adjust
2. Other warning lamps

2. See service manual

15

VI. Problems Detected by SMELL, SIGHT OR SOUND

(continued)
E. Warning buzzers
POSSIBLE CAUSE solution

1. Solvent leak / spill

1. Locate and correct

2. Other warning buzzers

2. See service manual

F. Squeaks and squeals

POSSIBLE CAUSE solution

1. Bearing failure

1. See service manual

2. Poor lubrication

2. Lubricate as necessary

3. Mechanical wear

3. See service manual

16

VII. key problem areas and preventive

maintenance
The chart below lists the most common problems that occur with each LC module.
In the right-hand column are listed preventive maintenance practices that can
reduce the failure rate. The numbers in parentheses are suggested intervals
between maintenance. The operators and service manuals for your LC may
have additional suggestions for preventive maintenance of your model of LC.

Reservoir
Problem preventive maintenance

1. Blocked inlet frit

1. a. Replace (3-6 mo.)
b. Filter mobile phase, 0.5 filter
2. Gas bubbles

2. Degas mobile phase

Pump
Problem preventive maintenance

1. Air bubbles

1. Degas mobile phase

2. Pump seal failure

2. Replace (3 mo.)

3. Check valve failure

3. Filter mobile phase, use inlet-line
frit. Keep spare

Injector
Problem preventive maintenance

1. Rotor seal wear

1. a. Dont overtighten
b. Filter samples

Column
Problem preventive maintenance

1. Blocked frit
1. a. Filter mobile phase
b. Filter samples
c. Use in-line filter and/or
guard column
2. Void at head of column
2. a. Avoid mobile phase pH > 8.
(Most silica-based columns)
b. Use guard column
c. Use precolumn
(saturator column)

17

VII. key problem areas and preventive

maintenance (continued)
Detector
Problem preventive maintenance

1. Lamp failure; decreased detector 1. Replace (6 mo.) or keep

response; increased detector noise spare lamp
2. Bubbles in cell
2. a. Keep cell clean
b. Use restrictor after cell
c. Degas mobile phase

General
Problem preventive maintenance

1. Corrosive/abrasive damage
1. Flush buffer from LC and clean
when not in use

18

warning: Contaminants can cause

High Backpressure
Split Peaks
Broad Peaks
Baseline Noise
Baseline Drift
Loss of Resolution
Irreversible Column Damage
System Damage

Protect your hplc column and results

Additional information can be found at
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valuable analytical columns and results from the damaging effect of contaminants.
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required

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Holder

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With the patented design, SecurityGuard
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If you are not completely satisfied with

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*Feature applies to analytical-sized guard system only, and
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19

SecurityGuard is a trademark of
Phenomenex, Inc.

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anfrage@
phenomenex.com

+31 (0)30-2418700
+31 (0)30-2383749
beinfo@
phenomenex.com

(800) 543-3681
(310) 328-7768
info@
phenomenex.com

4824 8048
4810 6265
dkinfo@
phenomenex.com

France
Parc des Grillons, Bat.3
60 route de Sartrouville
78232 Le Pecq Cedex
France

Germany
Zeppelinstr. 5
63741 Aschaffenburg
Germany

Ireland
Queens Avenue,
Hurdsfield Ind. Est.,
Macclesfield, Cheshire
SK10 2BN, UK

Italy
Via M. Serenari, 15/D
40013 Castel Maggiore (BO)
Italy

Luxembourg
Maarssenbroeksedijk 13D
3542 DL Utrecht
Netherlands

01 30 09 21 10
01 30 09 21 11
franceinfo@
phenomenex.com

06021-58830-0
06021-58830-11
anfrage@
phenomenex.com

01 247 5405
+44 1625-501796
eireinfo@
phenomenex.com

051 6327511
051 6327555
italiainfo@
phenomenex.com

+31 (0)30-2418700
+31 (0)30-2383749
nlinfo@
phenomenex.com

Netherlands
Maarssenbroeksedijk 13D
3542 DL Utrecht
Netherlands

New Zealand
P O Box 31-601
Milford 0741
North Shore City
New Zealand

Puerto Rico
273 Sierra Morena,
Suite #104
San Juan,
Puerto Rico 00926

United Kingdom
Queens Avenue,
Hurdsfield Ind. Est.,
Macclesfield, Cheshire
SK10 2BN, UK

USA
411 Madrid Ave.
Torrance, CA
90501-1430
USA

030-2418700
030-2383749
nlinfo@
phenomenex.com

09-4780951
09-4780952
nzinfo@
phenomenex.com

(800) 541-HPLC
(310) 328-7768
info@
phenomenex.com

01625-501367
01625-501796
ukinfo@
phenomenex.com

(310) 212-0555
(310) 328-7768
info@
phenomenex.com

6116_L

www.phenomenex.com
Phenomenex products are available worldwide. For the distributor in your country,
contact Phenomenex USA, International Department by telephone, fax or email: [email protected].