Triadimefon TC, EC, WP
Specification of Triadimefon TC, EC, WP in FAO SPECIFICATION 352 (October 2011*)
TRIADIMEFON TECHNICAL MATERIAL
FAO SPECIFICATION 352/TC (October 2011*)
This specification, which is PART ONE of this publication, is based on an evaluation of
data submitted by the manufacturer whose names are listed in the evaluation report
(352/2011). It should be applicable to TC produced by this manufacturer but it is not an
endorsement of those products, nor a guarantee that they comply with the specifications.
The specification may not be appropriate for TC produced by other manufacturers.
The evaluation report 352/2011, as PART TWO, forms an integral part of this publication.
1 Description
The material shall consist of triadimefon together with related manufacturing impurities
and shall be a white to greyish or yellowish grained powder free from visible extraneous
matter and added modifying agents.
2 Active ingredient
2.1 Identity tests (352/TC/M/2, CIPAC Handbook 1C, p. 2236, 1985)
The active ingredient shall comply with an identity test and, where the identity remains
in doubt, shall comply with at least one additional test.
2.2 Triadimefon content (352/TC/M/3, CIPAC Handbook 1C, p. 2237, 1985)
The triadimefon content shall be declared (not less than 960 g/kg) and, when determined,
the average measured content shall not be lower than the declared minimum
content.
TRIADIMEFON EMULSIFIABLE CONCENTRATE
FAO specification 352/EC (October 2011*)
This specification, which is PART ONE of this publication, is based on an evaluation of
data submitted by the manufacturer whose name is listed in the evaluation report
(352/2011). It should be applicable to relevant products of this manufacturer but it is
not an endorsement of those products, nor a guarantee that they comply with the specifications.
The specification may not be appropriate for the products of other manufacturers.
The evaluation report (352/2011) as PART TWO forms an integral part of this
publication.
.
1 Description
The material shall consist of technical triadimefon, complying with the requirements
of FAO specification 352/TC (October 2011), dissolved in suitable solvents, together
with any other necessary formulants. It shall be in the form of a stable homogeneous
clear liquid with light chestnut to brown color, free from visible suspended matter and
sediment, to be applied as an emulsion after dilution in water.
2 Active ingredient
2.1 Identity tests (352/EC/(M)/-, Note 1)
The active ingredient shall comply with an identity test and, where the identity
remains in doubt, shall comply with at least one additional test.
2.2 Triadimefon content (352/EC/(M)/-, Note 1)
The triadimefon content shall be declared (g/kg or g/L at 20 2 ºC, Note 2)
and, when determined, the average content measured shall not differ from declared
by more than the following tolerances.
Declared content in g/kg or g/L at 20 ±2°C Tolerance
above 25 up to 100 ±10% of the declared content
above 100 up to 250 ± 6% of the declared content
above 250 up to 500 ± 5% of the declared content
Note: In each range the upper limit is included
3 Physical properties
3.1 Emulsion stability and re-emulsification (CIPAC MT 36.3, Handbook K,
p.137, 2003)
The formulation, when diluted at 30 ± 2 °C with CIPAC Standard Waters A
and D, shall comply with the following:
Time after dilution Limits of stability, MT 36.3
0 h Initial emulsification complete
0.5 h "Cream", maximum: 1 mL
2.0 h "Cream", maximum: 1 mL
"Free oil", maximum: 0.1 mL
24 h Re-emulsification complete
24.5 h "Cream", maximum: 1 mL
"Free oil", maximum: 0.1 mL
Note: in applying MT 36.3, tests after 24 h are required only where results at 2 h are in doubt
3.2 Persistent foam (CIPAC MT 47.2, Handbook F, p.152, 1995) (Note 3)
Maximum: 50 mL after 1 min.
4 Storage stability
4.1 Stability at 0 °C (CIPAC MT 39.3, Handbook J, p. 126, 2000)
After storage at 0 ± 2 °C for 7 days, the volume of solid and/or liquid which
separates shall not be more than 0.3 mL.
4.2 Stability at elevated temperature (MT 46.3, Handbook J, p.128, 2000)
After storage at 54 ± 2 °C for 14 days, the determined average active ingredient
content must not be lower than 95 % relative to the determined average
content found before storage (Note 4) and the formulation shall continue to
comply with the clauses for:
- emulsion stability and re-emulsification (3.1).
TRIADIMEFON WETTABLE POWDER
FAO specification 352/WP (October 2011*)
This specification, which is PART ONE of this publication, is based on an evaluation of
data submitted by the manufacturer whose name is listed in the evaluation report
(352/2011). It should be applicable to relevant products of this manufacturer but it is
not an endorsement of those products, nor a guarantee that they comply with the specifications.
The specification may not be appropriate for the products of other manufacturers.
The evaluation report (352/2011) as PART TWO forms an integral part of this
publication.
1 Description
The material shall consist of a homogeneous mixture of technical triadimefon, complying
with the requirements of FAO specification 352/TC (October 2011), together
with filler(s) and any other necessary formulants. It shall be in the form of a white to
beige fine powder free from visible extraneous matter and hard lumps.
2 Active ingredient
2.1 Identity tests (352/WP/M/2, CIPAC Handbook 1C, p. 2236, 1985)
The active ingredient(s) shall comply with an identity test and, where the identity
remains in doubt, shall comply with at least one additional test.
2.2 Triadimefon content (352/WP/M/3, CIPAC Handbook 1C, p. 2239, 1985)
The triadimefon content shall be declared (g/kg) and, when determined, the
average content measured shall not differ from declared by more than the following
tolerances.
Declared content in g/kg Tolerance
above 25 up to 100 ±10% of the declared content
above 100 up to 250 ± 6% of the declared content
above 250 up to 500 ± 5% of the declared content
Note: In each range the upper limit is included
3 Physical properties
3.1 Wet sieve test (MT 185, CIPAC Handbook K, p.149, 2003)
Maximum: 2 % retained on a 75 μm test sieve.
3.2 Suspensibility (MT 184, CIPAC Handbook K, p.142, 2003)
A minimum of 60 % of the triadimefon content found under 2.2 shall be in
suspension after 30 min in CIPAC Standard Water D at 30 ± 2 °C.
3.3 Persistent foam (MT 47.2, CIPAC Handbook F, p.152, 1995)
Maximum: 10 mL after 1 min.
3.4 Wettability (MT 53.3, Handbook F, p.164, 1995)
The formulation shall be completely wetted in 120 sec. without swirling.
4 Storage stability
4.1 Stability at elevated temperature (MT 46.3, CIPAC Handbook J, p.128, 2000)
After storage at 54 ± 2 °C for 14 days, the determined average active ingredient
content must not be lower than 95 % relative to the determined average
content found before storage (Note 4) and the formulation shall continue to
comply with the clauses for:
- Wet sieve test (3.1),
- Suspensibility (3.2),
- Wettability (3.4),
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