WO2012074922A1 - Defense spray using isothiocyanate as an ingredient - Google Patents
Defense spray using isothiocyanate as an ingredient Download PDFInfo
- Publication number
- WO2012074922A1 WO2012074922A1 PCT/US2011/062236 US2011062236W WO2012074922A1 WO 2012074922 A1 WO2012074922 A1 WO 2012074922A1 US 2011062236 W US2011062236 W US 2011062236W WO 2012074922 A1 WO2012074922 A1 WO 2012074922A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- spray
- spray composition
- isothiocyanate
- subject
- defense
- Prior art date
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Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F41—WEAPONS
- F41H—ARMOUR; ARMOURED TURRETS; ARMOURED OR ARMED VEHICLES; MEANS OF ATTACK OR DEFENCE, e.g. CAMOUFLAGE, IN GENERAL
- F41H9/00—Equipment for attack or defence by spreading flame, gas or smoke or leurres; Chemical warfare equipment
- F41H9/10—Hand-held or body-worn self-defence devices using repellant gases or chemicals
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
- C06D7/00—Compositions for gas-attacks
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C331/00—Derivatives of thiocyanic acid or of isothiocyanic acid
- C07C331/16—Isothiocyanates
- C07C331/18—Isothiocyanates having isothiocyanate groups bound to acyclic carbon atoms
- C07C331/20—Isothiocyanates having isothiocyanate groups bound to acyclic carbon atoms of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C331/00—Derivatives of thiocyanic acid or of isothiocyanic acid
- C07C331/16—Isothiocyanates
- C07C331/18—Isothiocyanates having isothiocyanate groups bound to acyclic carbon atoms
- C07C331/22—Isothiocyanates having isothiocyanate groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
Definitions
- the present invention relates to non-lethal defense sprays and crowd control used by law enforcement, corrections institutions, military and security personnel to control resistive and/or violent subjects.
- defense sprays used by law enforcement, corrections institutions, military and security personnel to control resistive and/or violent subjects.
- defense sprays include CS tear gas, CN tear gas and red pepper spray.
- the defense spray must have an appropriate concentration of an active ingredient having the necessary stopping power.
- red pepper spray must have an appropriate concentration of capsaicinoids to provide the necessary stopping power. Understandably, the higher the concentration level of the capsaicinoid, the greater the stopping power.
- Pepper spray has been used as a less lethal inflammatory agent in law enforcement, security and military operations for several decades. It has a definite role for use by officers in controlling subject behavior. However, quite often, officers are hesitant to use pepper spray and other defensive sprays because of their long-lasting effects. The length of time in which the effects are felt is a significant concern given the likely possibility of contamination of fellow officers. Due to the dynamics of the confrontation, other officers may be accidentally sprayed resulting in them having to fight through the discomfort and distraction of the inflammatory agent. Due to the oily compounds and long lasting effects of most capsaicin-based (chili peppers) aerosols, some officers may themselves become incapacitated for a considerable amount of time by misdirected spray.
- compositions for a defense spray having an incapacitating effect of shorter duration include compositions for a defense spray having an incapacitating effect of shorter duration.
- an embodiment of the defense spray composition includes isothiocyanate as an active ingredient.
- the source of isothiocyanate can include wasabi, horseradish oil, or mustard. Alternatively, the isothiocyanate may be produced synthetically.
- Isothiocyanate has a high degree of volatility and readily evaporates.
- isothiocyanate as an active ingredient in compositions of the inventive defense spray, it produces an incapacitating effect on a subject that is of shorter duration than that associated with traditional defensive sprays, such as pepper spray and CS tear gas.
- the inventive defense spray composition provides a strategically useful tool in the deployment of non-lethal force that enables law enforcement and other like personnel to achieve their control objectives in an effective and efficient manner.
- the shorter duration of the incapacitating effect minimizes collateral disruptive effects that can otherwise be caused by a longer-lasting defense spray weapon.
- inventive defense spray composition permits relatively rapid decontamination so that accidentally-sprayed colleagues may quickly be treated for relief from the debilitating aspects of the spray, and controlled subjects may be quickly treated for relief from incapacitation so that they are physically able to cooperate with the apprehending personnel.
- the defense spray composition comprises a carrier solvent and an isothiocyanate compound of the formula: 6
- R may be selected from the group consisting of alkyl, alkenyl, allyl, and alkylthioalkyl.
- the defense spray composition may include propellants generally known to those skilled in the art.
- a weak acid may be included in the composition to provide stability and to control the volatility of the isothiocyanate ingredient.
- emulsifiers may be added to the composition to enhance the solubility of the ingredients.
- the defense spray composition comprises
- the solvent system can be comprised of 5% to 10% Propylene Glycol, 1% to 5% Polysorbate 80, 15% to 25%
- the composition may also contain other incapacitants such as CS Tear Gas, CN Tear gas or Oleoresin Capsicum (red pepper) with the Horseradish oil.
- the composition can be delivered via an aerosol propellant such as nitrogen, carbon dioxide, compressed air, HFC 134a (1,1,1,2-Tetrafluoroethane) or any other commercially available propellants.
- a marking dye may also be added to the composition.
- Another aspect of the invention is to provide a defense spray composition whereby the duration of the incapacitating effects can be controlled to have a shorter duration than that provided with other defense sprays such as red pepper.
- the duration of the incapacitating effects can be controlled.
- the defense spray composition of the present invention provides a strategic tool for law enforcement and correctional personnel by enabling the deployment of a non-lethal spray that delivers an incapacitating effect of relatively short duration. This feature promotes the achievement of rapid control of a subject while limiting cross- contamination of fellow personnel. A further advantage of the short duration in the effect of the inventive defense spray composition is to permit rapid decontamination of the affected subject once control is achieved.
- the inventive defense spray composition includes an isothiocyanate compound as an active ingredient.
- the formulation includes a solvent and an isothiocyanate compound of the formula sho n below.
- the substituent R group may be alkyl, alkenyl, allyl, or alkylthioalkyl.
- the R group may be allyl.
- alkenyl alone or in combination, refers to a substituted or unsubstituted straight-chain or substituted or unsubstituted branched- chain alkenyl group containing from 2 to 10 carbon atoms. Examples of such substituents include, but are not limited to, ethenyl, E- and Z-pentenyl, decenyl and the like.
- alkyl describes substituents which are preferably lower alkyl containing from one to eight carbon atoms in the principal chain and up to about 20 carbon atoms.
- the principal chain may be straight, branched or cyclic.
- Representative examples of alkyl include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, hexyl and the like.
- alkylthio describes an alkyl group, as described herein, appended to the parent molecular moiety through a sulfur atom.
- alkylthio include, but are not limited to, methylthio, ethylthio, tert-butylthio, and hexylthio.
- thio refers to a— S— moiety.
- the isothiocyanate compounds may be produced synthetically or isolated from plant sources. Plants belonging to the Brassicaceae family have high concentrations of isothiocyanates. Horseradish, (Armoracia lapathifolia Gilib., (Family: Cruciferae) Armoracia rusticana, syn. Cochlearia armoracia), wasabi, (Wasabia japonica, Cochlearia wasabi, or Eutrema japonica), and mustard (Brassica rapa, Brassica nigra, Brassica alba, Brassica carinata, Brassica oleracea), all have the particularly strong, pungent flavor indicative of isothiocyanates.
- Allyl isothiocyanate is commercially produced via the dry distillation of mustard seeds.
- a preferred embodiment of the present invention utilizes horseradish oil as the source of isothiocyanate.
- horseradish oil obtained from Synthite Industries LTD is a preferred source of horseradish oil.
- the spray composition may contain an isothiocyanate compound present in an amount of about 0.1 % to about 20% by weight of the formulation.
- the formulation may contain additional incapacitating agents known to those skilled in the art.
- the spray's "stopping power" and recovery time may be adjusted by varying the concentration of the isothiocyanate and other incapacitating agents present.
- the concentration of the active ingredients should be large enough to consistently produce the desired effect, but not so large as to cause undue injury, or result in an excessive recovery time.
- the formulation includes a solvent.
- the solvent system should uniformly dissolve or suspend the active ingredients. Preferred solvent systems are chemically stable, non-toxic, non-flammable, and safe for skin contact. Suitable solvents may include propylene glycol, ethanol, water, polypropylene glycol, polyethylene glycol, hydrogenated castor oil, mineral oil, vegetable oil, and mixtures thereof.
- the formulation may further include an emulsifier.
- an emulsifier for example, Polysorbate 80 is a preferred emulsifying agent.
- the defense spray composition comprises:
- Another preferred embodiment comprises:
- One preferred spray deployment embodiment comprises dispersing the spray as a fog or in a cone-shaped spray pattern.
- a preferred embodiment of the defense spray composition incorporating this dispersion feature comprises:
- Another preferred spray deployment embodiment comprises dispersing the spray under high-pressure propellant for more rapid evaporation after deployment.
- a preferred embodiment of the defense spray composition incorporating this dispersion feature comprises:
- the formulation may further include ultraviolet dyes or other marking agents in the spray composition.
- ultraviolet dyes or other marking agents in the spray composition.
- the spray leave a mark on the subject as a means to identify the subject as one having been sprayed.
- a sprayed subject may need to be later apprehended if he is able to withstand the initial spray and escape, but still pose a risk to others after flight.
- the marking effected by the spray helps in later identification of a subject.
- a preferred embodiment of the formulation of the defense spray composition in a 50 gallon batch incorporating this dispersion feature comprises:
- the spray composition of the present invention is very effectively employed as a means to temporarily incapacitate a subject for a relatively short period of duration.
- the subject is sprayed with the isothiocyanate composition in the normal manner as that for pepper spray.
- the volatile nature of the isothiocyanate compound causes the felt effects to diminish sooner than that experienced when sprayed by red pepper (or capsaicin).
- red pepper or capsaicin
- the inventive spray permits a more rapid decontamination of the subject so that his cooperation can be more readily obtained after the situation giving rise to the need for the spray deployment has been brought under control. This permits a more efficient apprehension and processing of a subject with minimal disruptive effect on law enforcement personnel.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- General Engineering & Computer Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A defense spray having an incapacitating effect of shorter duration is provided. The defense spray composition comprises isothiocyanate as an active ingredient. The source of the isothiocyanate can include wasabi, horseradish oil or mustard. Isothiocyanate has a high degree of volatility and readily evaporates. By incorporating isothiocyanate as an active ingredient in compositions of the inventive defense spray, it produces an incapacitating effect on a subject that is of shorter duration than that associated with traditional defensive sprays, such as pepper spray and CS tear gas.
Description
DEFENSE SPRAY USING ISOTHIOCYANATE AS AN INGREDIENT
RELATED APPLICATIONS
[0001] The present patent application claims priority benefit of an earlier-filed U.S. provisional patent application of the same title, Serial No. 61/417,597, filed November 29, 2010. The identified earlier-filed application is hereby incorporated by reference into the present application.
BACKGROUND OF THE INVENTION
[0002] 1. FIELD OF THE INVENTION
[0003] The present invention relates to non-lethal defense sprays and crowd control used by law enforcement, corrections institutions, military and security personnel to control resistive and/or violent subjects.
[0004] 2. DESCRIPTION OF THE PRIOR ART
[0005] There exist many types of non-lethal defense sprays used by law enforcement, corrections institutions, military and security personnel to control resistive and/or violent subjects. Such defense sprays include CS tear gas, CN tear gas and red pepper spray. When using such defense sprays, it is desirable and critical that they have sufficient "stopping power" in order to be effective in establishing control over the subject. To achieve that goal, the defense spray must have an appropriate concentration of an active ingredient having the necessary stopping power. For example, red pepper spray must have an appropriate concentration of capsaicinoids to provide the necessary stopping power. Understandably, the higher the concentration level of the capsaicinoid, the greater the stopping power.
[0006] Pepper spray has been used as a less lethal inflammatory agent in law enforcement, security and military operations for several decades. It has a definite role for use by officers in controlling subject behavior. However, quite often, officers are hesitant to use pepper spray and other defensive sprays because of their long-lasting effects. The length of time in which the effects are felt is a significant concern given the likely possibility of contamination of fellow officers. Due to the dynamics of the confrontation, other officers may be accidentally sprayed resulting in them having to fight through the discomfort and distraction of the inflammatory agent. Due to the oily compounds and long lasting effects of most capsaicin-based (chili peppers) aerosols, some officers may themselves become incapacitated for a considerable amount of time
by misdirected spray. If this occurs, the afflicted officers then become a protracted hazard to their own and the other assisting-officers' safety. Some aerosol defense sprays have a very long-lasting effect and can take an extremely long time to de-contaminate (even when using counter-acting decontamination solutions). Aside from the most important aspect (possible officer safety issues) this further results in a loss of productive time and effective resource management (such as immediate re-deployment of officers after the arrest).
[0007] Defense sprays may also render the intended subject incapacitated well beyond the time necessary to place the subject under control. With respect to red pepper spray, the higher the concentration level of capsaicinoids, the greater the stopping power. However, higher concentrations of capsaicinoids means a longer decontamination period. Once an offending subject is apprehended, it may be counterproductive for the apprehended subject to continue to suffer effects of the incapacitating spray if those effects render the subject unable to cooperate.
SUMMARY OF THE INVENTION
[0008] The present teachings include compositions for a defense spray having an incapacitating effect of shorter duration. In accordance with the invention, an embodiment of the defense spray composition includes isothiocyanate as an active ingredient. The source of isothiocyanate can include wasabi, horseradish oil, or mustard. Alternatively, the isothiocyanate may be produced synthetically.
[0009] Isothiocyanate has a high degree of volatility and readily evaporates. By incorporating isothiocyanate as an active ingredient in compositions of the inventive defense spray, it produces an incapacitating effect on a subject that is of shorter duration than that associated with traditional defensive sprays, such as pepper spray and CS tear gas. Accordingly, the inventive defense spray composition provides a strategically useful tool in the deployment of non-lethal force that enables law enforcement and other like personnel to achieve their control objectives in an effective and efficient manner. Furthermore, the shorter duration of the incapacitating effect minimizes collateral disruptive effects that can otherwise be caused by a longer-lasting defense spray weapon. The inventive defense spray composition permits relatively rapid decontamination so that accidentally-sprayed colleagues may quickly be treated for relief from the debilitating aspects of the spray, and controlled subjects may be quickly treated for relief
from incapacitation so that they are physically able to cooperate with the apprehending personnel.
[0010] In accordance with an aspect of the invention, the defense spray composition comprises a carrier solvent and an isothiocyanate compound of the formula: 6
wherein R may be selected from the group consisting of alkyl, alkenyl, allyl, and alkylthioalkyl. The defense spray composition may include propellants generally known to those skilled in the art.
[0011] In accordance with another aspect of the invention, a weak acid may be included in the composition to provide stability and to control the volatility of the isothiocyanate ingredient. Additionally, emulsifiers may be added to the composition to enhance the solubility of the ingredients.
[0012] In a preferred embodiment, the defense spray composition comprises
0.1% to 20% Horseradish oil, and a solvent system. The solvent system can be comprised of 5% to 10% Propylene Glycol, 1% to 5% Polysorbate 80, 15% to 25%
Ethanol, 50% to 65% water. The composition may also contain other incapacitants such as CS Tear Gas, CN Tear gas or Oleoresin Capsicum (red pepper) with the Horseradish oil. The composition can be delivered via an aerosol propellant such as nitrogen, carbon dioxide, compressed air, HFC 134a (1,1,1,2-Tetrafluoroethane) or any other commercially available propellants. A marking dye may also be added to the composition.
[0013] Another aspect of the invention is to provide a defense spray composition whereby the duration of the incapacitating effects can be controlled to have a shorter duration than that provided with other defense sprays such as red pepper. By modifying the concentration of the isothiocyanate ingredient, the duration of the incapacitating effects can be controlled.
[0014] These and other important features, aspects and advantages of the present teachings will become better understood with reference to the following description, examples and appended claims.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0015] The defense spray composition of the present invention provides a strategic tool for law enforcement and correctional personnel by enabling the deployment of a non-lethal spray that delivers an incapacitating effect of relatively short duration. This feature promotes the achievement of rapid control of a subject while limiting cross- contamination of fellow personnel. A further advantage of the short duration in the effect of the inventive defense spray composition is to permit rapid decontamination of the affected subject once control is achieved.
[0016] The inventive defense spray composition includes an isothiocyanate compound as an active ingredient. The formulation includes a solvent and an isothiocyanate compound of the formula sho n below.
[0017] The substituent R group may be alkyl, alkenyl, allyl, or alkylthioalkyl. In particular, the R group may be allyl. The term "alkenyl," alone or in combination, refers to a substituted or unsubstituted straight-chain or substituted or unsubstituted branched- chain alkenyl group containing from 2 to 10 carbon atoms. Examples of such substituents include, but are not limited to, ethenyl, E- and Z-pentenyl, decenyl and the like. The term "alkyl," as used herein, describes substituents which are preferably lower alkyl containing from one to eight carbon atoms in the principal chain and up to about 20 carbon atoms. The principal chain may be straight, branched or cyclic. Representative examples of alkyl include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, hexyl and the like. The term "alkylthio," as used herein, describes an alkyl group, as described herein, appended to the parent molecular moiety through a sulfur atom. Representative examples of alkylthio include, but are not limited to, methylthio, ethylthio, tert-butylthio, and hexylthio. The term "allyl," as used herein, refers to a— CH2CH=CH2 group. The term "thio," as used herein, refers to a— S— moiety.
[0018] The isothiocyanate compounds may be produced synthetically or isolated from plant sources. Plants belonging to the Brassicaceae family have high concentrations of isothiocyanates. Horseradish, (Armoracia lapathifolia Gilib., (Family: Cruciferae) Armoracia rusticana, syn. Cochlearia armoracia), wasabi, (Wasabia japonica, Cochlearia wasabi, or Eutrema japonica), and mustard (Brassica rapa, Brassica nigra, Brassica alba, Brassica carinata, Brassica oleracea), all have the particularly strong,
pungent flavor indicative of isothiocyanates. Allyl isothiocyanate is commercially produced via the dry distillation of mustard seeds. A preferred embodiment of the present invention utilizes horseradish oil as the source of isothiocyanate. For example, HORIOOO Oleoresin Horseradish obtained from Synthite Industries LTD is a preferred source of horseradish oil.
[0019] The spray composition may contain an isothiocyanate compound present in an amount of about 0.1 % to about 20% by weight of the formulation. The formulation may contain additional incapacitating agents known to those skilled in the art. The spray's "stopping power" and recovery time may be adjusted by varying the concentration of the isothiocyanate and other incapacitating agents present. The concentration of the active ingredients should be large enough to consistently produce the desired effect, but not so large as to cause undue injury, or result in an excessive recovery time. The formulation includes a solvent. The solvent system should uniformly dissolve or suspend the active ingredients. Preferred solvent systems are chemically stable, non-toxic, non-flammable, and safe for skin contact. Suitable solvents may include propylene glycol, ethanol, water, polypropylene glycol, polyethylene glycol, hydrogenated castor oil, mineral oil, vegetable oil, and mixtures thereof.
[0020] To help stabilize the volatility of the isothiocyanate compound, the formulation may further include an emulsifier. For example, Polysorbate 80 is a preferred emulsifying agent.
[0021] In a preferred embodiment, the defense spray composition comprises:
0.1% to 20% Horseradish oil
5% to 10% Propylene Glycol
1% to 5% Polysorbate 80
15% to 25% Ethanol
50% to 65% water.
[0022] Another preferred embodiment comprises:
1-20% Horseradish oil
50-90% HFC 134a Propellant
10-20% Propylene Glycol
30-40% Glycol Ether DB
[0023] One preferred spray deployment embodiment comprises dispersing the spray as a fog or in a cone-shaped spray pattern. A preferred embodiment of the defense spray composition incorporating this dispersion feature comprises:
5% Horseradish Oil
35% Glycol Ether DB
10% Propylene Glycol
50% HFC 134a
[0024] Another preferred spray deployment embodiment comprises dispersing the spray under high-pressure propellant for more rapid evaporation after deployment. A preferred embodiment of the defense spray composition incorporating this dispersion feature comprises:
5% Horseradish Oil
5% Glycol Ether DB
90% HFC 134a
[0025] In accordance with yet another aspect, the formulation may further include ultraviolet dyes or other marking agents in the spray composition. Given the relatively short duration of the incapacitating effect of the spray composition, it may be useful that the spray leave a mark on the subject as a means to identify the subject as one having been sprayed. A sprayed subject may need to be later apprehended if he is able to withstand the initial spray and escape, but still pose a risk to others after flight. The marking effected by the spray helps in later identification of a subject. A preferred embodiment of the formulation of the defense spray composition in a 50 gallon batch incorporating this dispersion feature comprises:
10.00% Horseradish oil - 5 gallons
25.00% Ethanol - 12.5 gallons
10.00% Propylene Glycol - 5 gallons
2.00% Polysorbate 80 - 1 gallon
0.50% D&C Green #8 Dye - 0.25 gallons
0.01% FD&C Green #3 Dye - 0.005 gallons
51.49% water - 25.745 gallons
1.00% UV Dye - 0.5 gallons
[0026] The spray composition of the present invention is very effectively employed as a means to temporarily incapacitate a subject for a relatively short period of duration. The subject is sprayed with the isothiocyanate composition in the normal manner as that for pepper spray. However, the volatile nature of the isothiocyanate compound causes the felt effects to diminish sooner than that experienced when sprayed by red pepper (or capsaicin). Because of the volatile nature of the inventive spray, there is less potential for mission-jeopardizing cross-contamination of law enforcement personnel from misdirected spray. Furthermore, the inventive spray permits a more rapid decontamination of the subject so that his cooperation can be more readily obtained after the situation giving rise to the need for the spray deployment has been brought under control. This permits a more efficient apprehension and processing of a subject with minimal disruptive effect on law enforcement personnel.
[0027] The detailed description set- forth above is provided to aid those skilled in the art in practicing the present invention. However, the invention described and claimed herein is not to be limited in scope by the specific embodiments herein disclosed because these embodiments are intended as illustration of several aspects of the invention. Any equivalent embodiments are intended to be within the scope of this invention. Indeed, various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art from the foregoing description which do not depart from the spirit or scope of the present inventive discovery.
[0028] Having thus described the preferred embodiments of the invention, what is claimed as new and desired to be protected by Letters Patent includes the following:
Claims
2. The spray composition according to Claim 1 in which R may be selected from the group consisting of alkyl, alkenyl, allyl, and alkylthioalkyl.
3. The spray composition according to Claim 1 in which the isothiocyanate compound is produced synthetically.
4. The spray composition according to Claim 1 in which the isothiocyanate compound is isolated from a Brassicaceae family plant source.
5. The spray composition according to Claim 4 in which the plant is selected from the group consisting of horseradish, wasabi and mustard.
6. A spray composition for temporarily incapacitating a subject, the spray composition comprising horseradish oil as an ingredient between 0.1% to 20% by weight of the spray composition.
7. The spray composition of Claim 6 in which the spray composition includes propylene glycol, ethanol, an emulsifier and water.
8. The spray composition of Claim 6 in which a propellant is added whereby the spray is adapted for dispersion as a fog spray pattern.
9. The spray composition of Claim 6 in which the spray comprises 5% horseradish oil, 5% glycol ether DB and 90% propellant, the propellant comprising HFC 134a, whereby the spray is adapted for rapid evaporation after deployment.
10. The spray composition according to Claim 6 in which a marker dye is added.
12. The method according to Claim 11 in which the R group in the spray composition may be selected from the group consisting of alkyl, alkenyl, allyl, and alkylthioalkyl.
13. The method according to Claim 11 in which the isothiocyanate is provided by a compound selected from the group consisting of horseradish, wasabi and mustard.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US41759710P | 2010-11-29 | 2010-11-29 | |
US61/417,597 | 2010-11-29 |
Publications (1)
Publication Number | Publication Date |
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WO2012074922A1 true WO2012074922A1 (en) | 2012-06-07 |
Family
ID=46172232
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/US2011/062236 WO2012074922A1 (en) | 2010-11-29 | 2011-11-28 | Defense spray using isothiocyanate as an ingredient |
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WO (1) | WO2012074922A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20180051964A1 (en) * | 2016-08-17 | 2018-02-22 | Forsythe & Storms Technologies LLC | Portable lachrymatory and electrical device |
WO2019036050A1 (en) * | 2017-08-18 | 2019-02-21 | Schepens Eye Research Institute | Compositions for the treatment of dry eye and methods of use thereof |
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US5248504A (en) * | 1992-03-02 | 1993-09-28 | Friedman William H | Method of treatment for nasal and sinus dysfunction |
US5334373A (en) * | 1991-07-18 | 1994-08-02 | Nippon Sanso Corporation | Allyl isothiocyanate sprays |
US20030170180A1 (en) * | 2001-11-13 | 2003-09-11 | Bahary William S. | Non-lethal chemical weapons |
US20060127996A1 (en) * | 2004-12-14 | 2006-06-15 | Johns Hopkins University | Method of extraction of isothiocyanates into oil from glucosinolate-containing plants and method of producing products with oil containing isothiocyanates extracted from glucosinolate-containing plants |
-
2011
- 2011-11-28 WO PCT/US2011/062236 patent/WO2012074922A1/en active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5334373A (en) * | 1991-07-18 | 1994-08-02 | Nippon Sanso Corporation | Allyl isothiocyanate sprays |
US5248504A (en) * | 1992-03-02 | 1993-09-28 | Friedman William H | Method of treatment for nasal and sinus dysfunction |
US20030170180A1 (en) * | 2001-11-13 | 2003-09-11 | Bahary William S. | Non-lethal chemical weapons |
US20060127996A1 (en) * | 2004-12-14 | 2006-06-15 | Johns Hopkins University | Method of extraction of isothiocyanates into oil from glucosinolate-containing plants and method of producing products with oil containing isothiocyanates extracted from glucosinolate-containing plants |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20180051964A1 (en) * | 2016-08-17 | 2018-02-22 | Forsythe & Storms Technologies LLC | Portable lachrymatory and electrical device |
WO2018035304A1 (en) * | 2016-08-17 | 2018-02-22 | Forsythe & Storms Technologies LLC | Portable lachrymatory and electrical device |
US10309753B2 (en) * | 2016-08-17 | 2019-06-04 | Forsythe & Storms Technologies LLC | Portable lachrymatory and electrical device |
WO2019036050A1 (en) * | 2017-08-18 | 2019-02-21 | Schepens Eye Research Institute | Compositions for the treatment of dry eye and methods of use thereof |
US11554104B2 (en) | 2017-08-18 | 2023-01-17 | The Schepens Eye Research Institute, Inc. | Compositions for the treatment of dry eye and methods of use thereof |
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