27314-13-2 Usage
Description
NORFLURAZON is a colorless, odorless crystalline solid or powder with non-corrosive properties. It is primarily used as an herbicide in the agricultural industry.
Uses
Used in Agricultural Industry:
NORFLURAZON is used as a selective preemergent herbicide for controlling germinating annual grasses, sedges, rushes, and broadleaf weeds in various crops such as fruits (cranberries, citrus, cherries, nectarines, apricots), grapevines, vegetables, nuts, cotton, peanuts, and soybeans. It is also utilized in non-agricultural and industrial areas for weed control. However, it has been forbidden for use in the European Union since July 25, 2003. NORFLURAZON is registered for use in the United States and is manufactured by Clariant Corporation, North Carolina.
Used in Pesticide Industry:
NORFLURAZON is used as a pesticide to help control and manage the growth of unwanted plants and weeds in agricultural settings, ensuring the protection and growth of desired crops.
Used in Food Additive Industry:
NORFLURAZON is also utilized as an additive in the food industry, where it serves various purposes such as enhancing the quality, taste, or appearance of the final product, as well as extending its shelf life.
Reactivity Profile
A trifluoromethyl pyridazinone derivative.
Trade name
EVITAL?; H 9789?; SAN 9789 H?;
SAN 97895?; SOLICAM?; TELOK?[C];
TRIETHANOLAMINE DBS?; ZORIAL?
Safety Profile
When heated to
decomposition emits toxic fumes of NOx,
F-, and Cl-.
Potential Exposure
Norflurazon is a pyridazinone selective
pre-emergent herbicide used to control germinating
annual grasses, sedges, rushes and broadleaf weeds in fruits
(cranberries, citrus, cherries, nectarines, apricots), grape
vines, vegetables, nuts, cotton, peanuts, soybeans, and various
nonagricultural and industrial areas. Forbidden for use
in the EU after 7/25/2003. Manufactured in the United
States by Clariant Corporation, North Carolina.
Shipping
UN3077 Environmentally hazardous substances,
solid, n.o.s., Hazard Class: 9; Labels: 9-Miscellaneous hazardous
material, Technical Name Required.
Incompatibilities
rapidly degraded by strong light; UV.
Incompatible with oxidizers, chlorates nitrates, peroxides.
Waste Disposal
It is the responsibility of
chemical waste generators to determine the toxicity and
physical properties and of a discarded chemical and to
properly identify its classification and certification as a
hazardous waste and to determine the disposal method.
United States Environmental Protection Agency guidelines
for the classification determination are listed in 40 CFR
Parts 261.3. Additionally, waste generators must consult
and follow all regional, national, state and local hazardous
waste laws to ensure complete and accurate classification
and disposal methods. Follow recommendations for the
disposal of pesticides and pesticide containers. Containers
must be disposed of properly by following package label
directions or by contacting your local or federal environmental
control agency, or by contacting your regional
EPA office.
Check Digit Verification of cas no
The CAS Registry Mumber 27314-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,1 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27314-13:
(7*2)+(6*7)+(5*3)+(4*1)+(3*4)+(2*1)+(1*3)=92
92 % 10 = 2
So 27314-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9ClF3N3O/c1-17-9-6-18-19(11(20)10(9)13)8-4-2-3-7(5-8)12(14,15)16/h2-6,17H,1H3
27314-13-2Relevant articles and documents
Substituted pyridinesulfonamide compound or its salt, process for preparing the same, and herbicide containing the same
-
, (2008/06/13)
A substituted pyridinesulfonamide compound or its salt represented by the following general formula (I): STR1 wherein A is CH or N; when A is CH, R1 and R2 may be either each independently a member selected from the group consisting of unsubstituted or substituted alkyl groups, unsubstituted or substituted alkenyl groups, unsubstituted or substituted cycloalkyl groups, and unsubstituted or substituted phenyl groups; when A is N, R1 is an unsubstituted or substituted alkyl group, R2 is an unsubstituted or substituted alkyl group, or an unsubstituted or substituted alkoxy group; and X and Y are each independently a member selected from the group consisting of alkyl groups and alkoxy groups, is disclosed. This compound is useful as the effective ingredient of a herbicide showing a wide weed-control spectrum even if used in a small amount.
SYNTHESIS, SPECTRAL PROPERTIES, AND PESTICIDAL ACTIVITY OF 4-AMINO(ALKYLAMINO, DIALKYLAMINO)-5-CHLORO-2-SUBSTITUTED-3-OXO-2H-PYRIDAZINES AND 5-AMINO(ALKYLAMINO, DIALKYLAMINO)-4-CHLORO-2-SUBSTITUTED-3-OXO-2H-PYRIDAZINES
Konecny, Vaclav,Kovac, Stefan,Varkonda, Stefan
, p. 492 - 502 (2007/10/02)
4-Amino(alkylamino)-5-chloro-2-substituted-3-oxo-2H-pyridazines and 5-amino(alkylamino, dialkylamino)-4-chloro-2-substituted-3-oxo-2H-pyridazines have been prepared by nucleophilic substitution reactions of 4,5-dichloro-2-substituted-3-oxo-2H-pyridazines with amines in aprotic solvent.Structure of the compounds prepared has been proved by IR and UV spectra.Fungicidal and herbicidal activity of the compounds prepared have been tested.None of the compounds prepared exceeds the standard Vitavax in the fungicidal activity tests.Compounds VIII and XII show equal or better activity on the Hill reaction as compared with the standard pyrazone.
