Acute toxicity - Category 4, Oral
Acute toxicity - Category 4, Dermal
H302 Harmful if swallowed
H312 Harmful in contact with skin
P264 Wash ... thoroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P301+P317 IF SWALLOWED: Get medical help.
P330 Rinse mouth.
P302+P352 IF ON SKIN: Wash with plenty of water/...
P317 Get medical help.
P321 Specific treatment (see ... on this label).
P362+P364 Take off contaminated clothing and wash it before reuse.
none
P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.
no data available
Fresh air, rest.
Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth. Refer for medical attention .
Inhalation of spray and prolonged or repeated contact with skin should be avoided. (EPA, 1998)
Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR if necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on the left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. Poisons A and B
Non-Specific -- Poisonous Solid, n.o.s.) For small fires, use dry chemical, carbon dioxide, water spray, or foam. For large fires, use water spray, fog, or foam. (EPA, 1998)
Flash point data for this chemical are not available; however, it is probably combustible. (NTP, 1992)
In case of fire in the surroundings, use appropriate extinguishing media.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. Carefully collect remainder. Then store and dispose of according to local regulations.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. Carefully collect remainder. Then store and dispose of according to local regulations.
Sweep spilled substance into containers. Carefully collect remainder, then remove to safe place. Do NOT let this chemical enter the environment. (Extra personal protection: P2 filter respirator for harmful particles).
Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.
Dry. Keep in a well-ventilated room. Store in glass, high-density plastic, rubber or epoxy resin-protected metal containers.Pesticide Storage: Store in original container. DO NOT store below freezing temperatures.
no data available
no data available
Ensure adequate ventilation. Handle in accordance with good industrial hygiene and safety practice. Set up emergency exits and the risk-elimination area.
Wear face shield or eye protection in combination with breathing protection.
Protective gloves. Protective clothing.
Use local exhaust or breathing protection.
no data available
Chlormequat chloride is a white crystals with a fishlike odor. Used as a plant growth regulator. Said to be effective for cereal grains, tomatoes, and peppers. (EPA, 1998)
White cyrstalline solid
TYPICAL AMINE ODOR
117°C(lit.)
175°C/27mmHg(lit.)
Not combustible. Gives off irritating or toxic fumes (or gases) in a fire.
no data available
46°C(lit.)
no data available
245°C
pH = 5.14
no data available
greater than or equal to 100 mg/mL at 73° F (NTP, 1992)
log Kow = -3.80
7.5e-08 mm Hg at 68° F (NTP, 1992)
1.14 to 1.15 g/mL at 20 deg C
no data available
no data available
Decomposes on heating. This produces toxic and corrosive fumes including nitrogen oxides and hydrogen chloride. Decomposes on heating with strong aqueous alkali solutions. This produces trimethylamine and other gaseous products. Attacks many metals in the presence of water.
Stable up to 50 deg C for at least 2 years.
Noncombustible solid.CHLORMEQUAT CHLORIDE is incompatible with strong oxidizing agents. It is corrosive to unprotected metals. (NTP, 1992) Quaternary ammonium salts often serve as catalysts in reactions. They are incompatible with many strong oxidizers and reducing agents, such as metal hydrides, alkali/active metals, and organometallics.
no data available
Should not be combined with dinoseb, cyanazine, or other contact herbicides.
The substance decomposes on heating producing toxic and corrosive fumes including nitrogen oxides, hydrogen chloride. The substance decomposes on heating with strong aqueous alkali solutions producing trimethylamine and other gaseous products.
no data available
no data available
no data available
no data available
no data available
no data available
The aerosol is mildly irritating to the eyes. The substance may cause effects on the nervous system, cholinergic symptoms without acetylcholinesterase inhibition. See Notes.
no data available
Evaporation at 20°C is negligible; a harmful concentration of airborne particles can, however, be reached quickly when dispersed.
AEROBIC: In soil, chlormequat chloride is rapidly degraded by microbial activity and has no influence on soil microflora or fauna(1). Half-lives in 4 soils were reported as averaging 32 days at 10 deg C and 1 to 28 days at 22 deg C(1). Studies with soil microorganisms indicated that chlormequat chloride breakdown occurred through oxidative processes(2). Chlormequat chloride, at an initial concentration of 282 ppm, biodegraded 18% after running a compost operation consisting of poultry and pig manure for 56 days; the high concentration may have retarded degradation(3). Based on analogy to other quaternary ammonium compounds(4), the reduction of biomass or other nutrient materials in natural water may reduce the biodegradation rate of the chlormequat chloride cation and acclimation enhances biodegradation of quaternary ammonium compounds.
An estimated BCF of 3.2 was calculated for chlormequat chloride(SRC), using a log Kow of -3.80(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
The Koc of chlormequat chloride has been reported to be 203(1). According to a classification scheme(2), this Koc value suggests that chlormequat chloride is expected to have moderate mobility in soil. However, this compound exists as a quaternary ammonium cation and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(3). Chlormequat chloride is expected to adsorb strongly to various materials, including suspended solids in wastewater treatment facilities, sediments in rivers and lakes, suspended organics and minerals in natural water systems, clays, proteins, and microorganisms(4-6). Further, adsorption of quaternary ammonium compounds to river sediment occurs primarily by an ion-exchange mechanism(5). Monitoring studies of river water samples from Germany reported that 50% of an alkyltrimethyl quaternary ammonium compound detectable in the water column was associated with suspended solids in the water; the suspended solids in the water comprise a small fraction of the water(7).
no data available
The material can be disposed of by removal to a licensed chemical destruction plant or by controlled incineration with flue gas scrubbing. Do not contaminate water, foodstuffs, feed or seed by storage or disposal. Do not discharge to sewer systems.
Containers can be triply rinsed (or equivalent) and offered for recycling or reconditioning. Alternatively, the packaging can be punctured to make it unusable for other purposes and then be disposed of in a sanitary landfill. Controlled incineration with flue gas scrubbing is possible for combustible packaging materials.
ADR/RID: Not dangerous goods. (For reference only, please check.)
IMDG: Not dangerous goods. (For reference only, please check.)
IATA: Not dangerous goods. (For reference only, please check.)
ADR/RID: Not dangerous goods. (For reference only, please check.)
IMDG: Not dangerous goods. (For reference only, please check.)
IATA: Not dangerous goods. (For reference only, please check.)
ADR/RID: Not dangerous goods. (For reference only, please check.)
IMDG: Not dangerous goods. (For reference only, please check.)
IATA: Not dangerous goods. (For reference only, please check.)
ADR/RID: Not dangerous goods. (For reference only, please check.)
IMDG: Not dangerous goods. (For reference only, please check.)
IATA: Not dangerous goods. (For reference only, please check.)
ADR/RID: No
IMDG: No
IATA: No
no data available
no data available
Use of atropine as specific treatment is contraindicated.If the substance is formulated with solvents also consult the ICSCs of these materials.Carrier solvents used in commercial formulations may change physical and toxicological properties.