Interim Revision Announcement

Official September 1, 2012

Benzalkonium

Table 1

Benzalkonium Chloride Solution

DEFINITION
Benzalkonium Chloride Solution contains NLT 95.0% and
NMT 105.0% of the labeled amount of benzalkonium
chloride in a solution having a concentration of 1.0% or
more; and NLT 93.0% and NMT 107.0% of the labeled
amount of benzalkonium chloride in a solution having a
concentration of less than 1.0%. It may contain a suitable coloring agent and may contain NMT 10% of
alcohol.
[CAUTIONMixing Benzalkonium Chloride Solution with
ordinary soaps and anionic detergents may decrease or destroy the bacteriostatic activity of the Solution.]
IDENTIFICATION
A.
Analysis: To 2 mL of a solution having an equivalent of
10 mg/mL of benzalkonium chloride add 1 mL of 2 N
nitric acid.
Acceptance criteria: A white precipitate is formed, and
is dissolved after adding 5 mL of alcohol.
B. IDENTIFICATION TESTSGENERAL, Chloride 191: A solution of it in a mixture of equal volumes of water and
alcohol meets the requirements.
C.
Analysis: Dissolve the residue obtained by evaporating
on a steam bath a volume of Solution equivalent to 200
mg of benzalkonium chloride in 1 mL of sulfuric acid.
Add 100 mg of sodium nitrate, and heat on a steam
bath for 5 min. Cool, dilute with water to 10 mL, add
500 mg of zinc dust, and warm for 5 min on a steam
bath. To 2 mL of the clear supernatant add 1 mL of
sodium nitrite solution (1 in 20), cool in ice water, then
add 3 mL of a solution of 500 mg of 2-naphthol in 10
mL of 6 N ammonium hydroxide.
Acceptance criteria: An orange-red color is produced.
D. The retention times of the major peaks for benzalkonium chloride of the Sample solution correspond to
those of the Standard solution, as obtained in the test for
Ratio of Alkyl Components.
ASSAY
RATIO OF ALKYL COMPONENTS
Solution A: Adjust a 0.1 M solution of sodium acetate
with glacial acetic acid to a pH of 5.0.
Mobile phase: Acetonitrile and Solution A (9:11). Acetonitrile and Solution A may be adjusted from (2:3) to
(3:2) to meet system suitability requirements.
Standard solution: 4 mg/mL of benzalkonium chloride,
prepared from USP Benzalkonium Chloride RS and water
Sample solution: Transfer a volume of Solution, equivalent to 400 mg of benzalkonium chloride, to a 100-mL
volumetric flask, and dilute with water to volume.
Chromatographic system
(See Chromatography 621, System Suitability.)
Mode: LC
Detector: UV 254 nm
Column: 3.9-mm 30-cm; packing L10, or 4.6-mm
25-cm; 10-m packing L10
Flow rate: 2 mL/min
Injection volume: 20 L
System suitability
Sample: Standard solution
[NOTESee Table 1. Relative retention times are provided for information only, and the Standard should
be used to ensure appropriate peak identification.]

Name
C10
C12
C14
C16

homolog
homolog
homolog
homolog

Relative
Retention
Time
0.9
1.0
1.3
1.7

Suitability requirements
Resolution: NLT 1.5 between the C12 and C14
homologs
Relative standard deviation: NMT 2.0% for the C12
homolog
Analysis
Samples: Standard solution and Sample solution
Identify the homolog peaks by comparison of the retention times of the Sample solution with those of the
Standard solution.
Calculate the percentage of each quaternary ammonium
homolog in the portion of Solution taken:

rU

= peak area of each homolog from the Sample

solution
Mr
= molecular weight of each homolog. The
molecular weights of the C10, C12, C14, and
C16 homologs are 312, 340, 368, and 396,
respectively.
Acceptance criteria: On the solid basis, the content of
the n-C12H25 homolog is NLT 40.0%, and the content of
the n-C14H29 homolog is NLT 20.0% of the total
alkylbenzyldimethylammonium chloride content. The
amount of the n-C12H25 and n-C14H29 homolog
components together is NLT 70.0% of the total
alkylbenzyldimethylammonium chloride content.
Change to read:

TOTAL ALKYLBENZYLDIMETHYLAMMONIUM CHLORIDES

Sample solution: Evaporate or dilute with water to 30
mL a volume of Solution equivalent to 500 mg of
benzalkonium chloride.
Analysis: Transfer the Sample solution, with the aid of a
minimum quantity of water, to a glass-stoppered, 250mL conical separator. Transfer 25 mL of methylene
chloride. Add 10 mL of 0.1 N sodium hydroxide, and
10.0 mL of freshly prepared potassium iodide solution
(1 in 20), insert the stopper in the separator, shake,
allow the layers to separate, and discard the methylene
chloride layer. Wash the aqueous layer with three 10-mL
portions of methylene chloride, and discard the
washings. Transfer the aqueous layer to a glassstoppered, 250-mL conical flask, and rinse the separator
with three 5-mL portions of water, adding the washings
to the flask. Add 40 mL of cold hydrochloric acid to the
flask, mix, and titrate with 0.05 M potassium iodate VS
until the solution becomes light brown in color. Add 5
mL of methylene chloride, insert the stopper into the
flask, and shake vigorously. Continue the titration,
dropwise, with shaking after each addition, until the
methylene chloride layer no longer changes color (IRA
1-Sep-2012) and the aqueous layer is clear yellow. Record
the titrant volume, Vt, in mL. Perform a blank
determination, using 20 mL of water as the sample, and
record the titrant volume, Vb, in mL. [NOTEVb > Vt.]
The difference between the two titrations represents the

2012 The United States Pharmacopeial Convention All Rights Reserved.

Interim Revision Announcement

Official September 1, 2012

Benzalkonium
amount of potassium iodate equivalent to the weight of
benzalkonium chloride in the sample. Each mL of 0.05
M potassium iodate is equivalent to x/10 mg of
benzalkonium chloride, where x represents the average
molecular weight of the sample, derived by summing,
for all homologs, the products:

rU

= peak area of each homolog from the Ratio of

Alkyl Components test
rT
= sum of all the peak areas of the homologs
from the Ratio of Alkyl Components test
Mr
= molecular weight of each homolog. The
molecular weights of the C10, C12, C14, and
C16 homologs are 312, 340, 368, and 396,
respectively.
Acceptance criteria
For labeled concentrations of NLT 1.0%:
95.0%105.0%
For labeled concentrations less than 1.0%:
93.0%107.0%
OTHER COMPONENTS
Change to read:

ALCOHOL CONTENT (if added)

Internal standard solution: 0.06 mL/mL of tertiary
butyl alcohol in water
Alcohol stock solution: 0.015 mL/mL of alcohol
(C2H5OH) in water, from USP Alcohol
DeterminationAlcohol RS (IRA 1-Sep-2012)
Standard solutions: Introduce 10, 20, and 40 mL, (IRA
1-Sep-2012) respectively, of Alcohol stock solution into three
separate identical 50-mL volumetric flasks. To each flask
add a 5-mL portion of the Internal standard solution.
Dilute with water to volume, and mix thoroughly. The
Standard solutions contain 0.003, 0.006, and 0.012
mL/mL of alcohol (C2H5OH), respectively.
Sample solution: Weigh an appropriate amount of
Solution into a 50-mL volumetric flask, and pipet 5 mL
of the Internal standard solution into the flask. Dilute
with water to volume, and mix thoroughly to obtain a
solution containing 0.0030.012 mL/mL of alcohol
(C2H5OH).
Chromatographic system
(See Chromatography 621, System Suitability.)
Mode: GC
Detector: Flame ionization
Column: 0.25-mm 30-m glass or quartz capillary;
1.4-m layer of phase G43
Temperatures
Detector: 250
Injection port: 250
Column: See Table 2.
Table 2
Initial
Temperature
()
40
40

Temperature
Ramp
(/min)

30

Final
Temperature
()
40
250

Hold Time
at Final
Temperature
(min)
7
15

Run time: 29 min

Carrier gas: Helium or nitrogen
Flow rate: See Table 3.
Table 3

Initial Flow
(mL/min)
1
1

Flow Ramp
(mL/min2)

10

Final Flow
(mL/min)
1
3

Hold Time
at
Final Flow
(min)
8
21

Injection volume: 1 L
Injection type: Split 75:1
System suitability
Sample: Standard solution containing 0.006 mL/mL of
alcohol (C2H5OH)
[NOTEThe relative retention times for alcohol and
tertiary butyl alcohol are 0.7 and 1.0, respectively.]
Suitability requirements
Resolution: NLT 2.0 between alcohol and tertiary
butyl alcohol
Relative standard deviation: NMT 10%
Analysis
Samples: Standard solutions and Sample solution
Plot the peak response ratios of the alcohol to tertiary
butyl alcohol in the Standard solutions versus the
content, in mL/mL, of alcohol, and draw the straight
line best fitting the plotted points. From the graph
obtained, determine the content, C, in mL/mL, of
alcohol (C2H5OH) in the Sample solution.
Calculate the percentage of alcohol (C2H5OH) in the
portion of Solution (v/v) taken:
Result = V (C D/W) 100
V
D

= volume of the Sample solution, 50 mL

= density of Benzalkonium Chloride Solution
(g/mL)
W
= weight of Benzalkonium Chloride Solution
taken to prepare the Sample solution (g)
Acceptance criteria: If present, 95.0%105.0% of the
labeled amount of alcohol (C2H5OH)
IMPURITIES
LIMIT OF AMINES AND AMINE SALTS
Sample: A quantity of Solution equivalent to 5.0 g of
benzalkonium chloride
Analysis: Dissolve the Sample by heating carefully (e.g.,
on top of a steam bath with water as the steam source)
in 20 mL of a mixture of methanol and 1 N
hydrochloric acid VS (97:3). [NOTEThe mixed solution,
however, must not reach the boiling point.] Add 100
mL of isopropyl alcohol, and pass a stream of nitrogen
slowly through the solution. Gradually add 12.0 mL of
0.1 N tetrabutylammonium hydroxide VS while
recording the potentiometric titration curve.
Acceptance criteria: If the curve shows two inflection
points, the volume of titrant added between the two
points is NMT 5.0 mL, corresponding to NMT 0.1
mmol/g of amines and amine salts. If the curve shows
no point of inflection, the substance being examined
does not comply with the test. If the curve shows one
point of inflection, repeat the test, but add 3.0 mL of a
25.0 mg/mL solution of dimethyldecylamine in
isopropyl alcohol before the titration. If after the
addition of 12.0 mL of the titrant, the titration curve
shows only one point of inflection, the substance being
examined does not comply with the test.
LIMIT OF BENZYL ALCOHOL, BENZALDEHYDE, AND
(CHLOROMETHYL)BENZENE

2012 The United States Pharmacopeial Convention All Rights Reserved.

Interim Revision Announcement

Official September 1, 2012

Benzalkonium

[NOTEPrepare the solutions immediately before use.]

Solution A: Dissolve 1.09 g of sodium 1hexanesulfonate and 6.9 g of monobasic sodium
phosphate in water in a 1000-mL volumetric flask,
adjust with phosphoric acid to a pH of 3.5, and dilute
with water to volume.
Solution B: Methanol
Mobile phase: See Table 4.
Table 4
Time
(min)
0
10
14
35
36
55
56
65

Solution A
(%)
80
80
50
50
20
20
80
80

Solution B
(%)
20
20
50
50
80
80
20
20

Standard solution A: 0.25 mg/mL of USP Benzyl

Alcohol RS in methanol
Standard solution B: 0.075 mg/mL of USP
Benzaldehyde RS in methanol
Standard solution C: 0.025 mg/mL of USP Benzyl
Alcohol RS in methanol, prepared from Standard solution
A and methanol
Sample solution: Determine the density of the Solution.
Dilute a quantity of the Solution equivalent to 2.5 g of
benzalkonium chloride with methanol to 50.0 mL. This
solution contains 50 mg/mL of benzalkonium chloride.
Chromatographic system
(See Chromatography 621, System Suitability.)
Mode: LC
Detector: UV 210 nm for benzyl alcohol and
(chloromethyl)benzene; UV 257 nm for benzaldehyde
Column: 4.6-mm 15-cm; 5-m packing L1
Column temperature: 30
Flow rate: 1.0 mL/min
Injection volume: 20 L
System suitability
Samples: Standard solution A, Standard solution B,
Standard solution C, and Sample solution
[NOTESee Table 5 for relative retention times.]
Table 5

Name
Benzyl alcohol
Benzaldehyde
(Chloromethyl)benzene

Relative
Retention
Time
1.0
1.3
2.4

Analysis
Samples: Standard solution A, Standard solution B,
Standard solution C, and Sample solution
Calculate the content of (chloromethyl)benzene by
multiplying the peak area of (chloromethyl)benzene by
1.3. [NOTEThe correction factor is used to adjust for
baseline shift.]
Acceptance criteria
Benzyl alcohol: The response of the benzyl alcohol
peak from the Sample solution is NMT that of the
benzyl alcohol peak from Standard solution A,
corresponding to NMT 0.5%.
Benzaldehyde: The response of the benzaldehyde
peak from the Sample solution is NMT that of the
benzaldehyde peak from Standard solution B,
corresponding to NMT 0.15%.
(Chloromethyl)benzene: The response of the
(chloromethyl)benzene peak from the Sample solution
is NMT 0.1 times that of the principal peak from
Standard solution A, corresponding to NMT 0.05%.
SPECIFIC TESTS
MICROBIAL ENUMERATION TESTS 61 and TESTS FOR
SPECIFIED MICROORGANISMS 62: A solution containing
less than 5.0% of benzalkonium chloride meets the
requirements of the test for absence of Pseudomonas
aeruginosa.
Change to read:

ACIDITY OR ALKALINITY
Sample solution: Evaporate or dilute with carbon
dioxide-free water to prepare a 50-mL solution of 10
mg/mL of benzalkonium chloride in water. (IRA 1-Sep-2012)
Analysis: To the Sample solution add 0.1 mL of
bromocresol purple TS.
Acceptance criteria: NMT 0.5 mL (IRA 1-Sep-2012) of 0.1
N hydrochloric acid or 0.1 N sodium hydroxide is
required to change the color of the indicator.
ADDITIONAL REQUIREMENTS
PACKAGING AND STORAGE: Preserve in tight containers,
and prevent contact with metals.
LABELING: Label it to indicate the concentration of
benzalkonium chloride, and to indicate the name and
quantity of the coloring agent added. The labeling also
indicates the concentration of alcohol added.
Change to read:

USP REFERENCE STANDARDS 11

USP Alcohol DeterminationAlcohol RS (IRA 1-Sep-2012)
USP Benzaldehyde RS
USP Benzalkonium Chloride RS
USP Benzyl Alcohol RS

Suitability requirements
Relative standard deviation: NMT 5.0% for benzyl
alcohol, Standard solution A
Signal-to-noise ratio: NLT 10 for the principal peak,
Standard solution C

2012 The United States Pharmacopeial Convention All Rights Reserved.