Acute toxicity - Category 3, Oral
Acute toxicity - Category 3, Dermal
Skin irritation, Category 2
Serious eye damage, Category 1
Acute toxicity - Category 2, Inhalation
Specific target organ toxicity – single exposure, Category 3
Carcinogenicity, Category 2
Specific target organ toxicity – repeated exposure, Category 1
Hazardous to the aquatic environment, short-term (Acute) - Category Acute 1
Hazardous to the aquatic environment, long-term (Chronic) - Category Chronic 1
Reproductive toxicity, Category 2
H301 Toxic if swalloed
H311 Toxic in contact with skin
H315 Causes skin irritation
H318 Causes serious eye damage
H330 Fatal if inhaled
H335 May cause respiratory irritation
H351 Suspected of causing cancer
H361 Suspected of damaging fertility or the unborn child
H371 May cause damage to organs
H372 Causes damage to organs through prolonged or repeated exposure
H400 Very toxic to aquatic life
H410 Very toxic to aquatic life with long lasting effects
P201 Obtain special instructions before use.
P260 Do not breathe dust/fume/gas/mist/vapours/spray.
P273 Avoid release to the environment.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P320 Specific treatment is urgent (see … on this label).
P330 Rinse mouth.
P304+P340 IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405 Store locked up.
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/...
P260 Do not breathe dust/fume/gas/mist/vapours/spray.
P271 Use only outdoors or in a well-ventilated area.
P284 [In case of inadequate ventilation] wear respiratory protection.
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P203 Obtain, read and follow all safety instructions before use.
P273 Avoid release to the environment.
P301+P316 IF SWALLOWED: Get emergency medical help immediately.
P321 Specific treatment (see ... on this label).
P330 Rinse mouth.
P302+P352 IF ON SKIN: Wash with plenty of water/...
P316 Get emergency medical help immediately.
P361+P364 Take off immediately all contaminated clothing and wash it before reuse.
P332+P317 If skin irritation occurs: Get medical help.
P362+P364 Take off contaminated clothing and wash it before reuse.
P305+P354+P338 IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P317 Get medical help.
P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.
P320 Specific treatment is urgent (see ... on this label).
P319 Get medical help if you feel unwell.
P318 IF exposed or concerned, get medical advice.
P391 Collect spillage.
P405 Store locked up.
P403+P233 Store in a well-ventilated place. Keep container tightly closed.
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. Refer for medical attention.
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.
Give a slurry of activated charcoal in water to drink. Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Give one or two glasses of water to drink. Refer for medical attention .
SYMPTOMS: Symptoms of exposure to this compound may include skin and mucous membrane irritation, glycosuria, hyperglycemia, dizziness, blurred vision, transient loss of consciousness and convulsions. Common symptoms are severe headaches, nausea, vomiting and epigastric pain. ACUTE/CHRONIC HAZARDS: This compound causes skin irritation on contact. When heated to decomposition (above 113° F) it emits acrid smoke and fumes. (NTP, 1992)
Exposure by inhalation: Fresh air, rest. Refer for medical attention. Exposure to skin: Remove contaminated clothes. Rinse & then wash skin with water & soap. Refer for medical attention. Exposure to eyes: First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then take to a doctor. Exposure by ingestion: Give plenty of water to drink. Refer for medical attention. from table
Use/ powder, water spray, foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
Flash point data for this chemical are not available; however, it is probably combustible. (NTP, 1992)
Use water spray, powder, foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
HEALTH | 4 | Very short exposure could cause death or major residual injury (e.g. hydrogen cyanide, phosgene, methyl isocyanate, hydrofluoric acid) | |
FIRE | 1 | Materials that require considerable preheating, under all ambient temperature conditions, before ignition and combustion can occur. Includes some finely divided suspended solids that do not require heating before ignition can occur. Flash point at or above 93.3 °C (200 °F). (e.g. mineral oil, ammonia) | |
REACT | 0 | Normally stable, even under fire exposure conditions, and is not reactive with water (e.g. helium,N2) | |
SPEC. HAZ. |
Personal protection: face shield, chemical protection suit and particulate filter respirator adapted to the airborne concentration of the substance. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations. Do NOT let this chemical enter the environment.
Personal protection: face shield, chemical protection suit and particulate filter respirator adapted to the airborne concentration of the substance. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations. Do NOT let this chemical enter the environment.
The compounds should not be allowed to enter drains or watercourses. Triphenyltin compounds
NO open flames. 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.
Provision to contain effluent from fire extinguishing. Separated from food and feedstuffs. Store in an area without drain or sewer access.Provision to contain effluent from fire extinguishing. /Store/ separated from food & feedstuffs.
Component | Fentin hydroxide | |||
---|---|---|---|---|
CAS No. | 76-87-9 | |||
Limit value - Eight hours | Limit value - Short term | |||
ppm | mg/m3 | ppm | mg/m3 | |
Germany (AGS) | 0,0004 (1) | 0,002 (1) | 0,0008 (1)(2) | 0,004 (1)(2) |
Remarks | ||||
Germany (AGS) | (1) Inhalable fraction and vapour (2) 15 minutes average value |
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 safety goggles or eye protection in combination with breathing protection.
Protective gloves. Protective clothing.
Use ventilation, local exhaust or breathing protection.
no data available
ODORLESS
118-120°C
no data available
Combustible. Liquid formulations containing organic solvents may be flammable.
no data available
400 deg C
no data available
no data available
no data available
no data available
log Kow = 3.53
3.5e-07 mm Hg at 122° F (NTP, 1992)
1.54
no data available
no data available
no data available
Stable in the dark at room temperature. dehydration may occur on heating above 45 deg c. slowly decomp by sunlight, & more rapidly by u.v. light .
Combustible. Liquid formulations containing organic solvents may be flammable. NO open flames.TRIPHENYLTIN HYDROXIDE is sensitive to temperatures above 113°F and prolonged exposure to light. Incompatible with strongly acidic compounds. Also incompatible with oils used in oil spray formulations (NTP, 1992).
no data available
Surfactants, spreaders, or stickers should not be added because phytotoxicity may result. Do not use with oil sprays.
When heated to decomp it emits acrid smoke and fumes.
no data available
no data available
no data available
no data available
Cancer Classification: Group B2 Probable Human Carcinogen
no data available
The substance is severely irritating to the eyes. The substance is irritating to the skin and respiratory tract. The substance may cause effects on the central nervous system.
The substance may have effects on the immune system. This may result in impaired functions. Animal tests show that this substance possibly causes toxicity to human reproduction or development.
A harmful concentration of airborne particles can be reached quickly on spraying or when dispersed, especially if powdered.
Triphenyltin hydroxide may be susceptible to biodegradation based upon the biodegradability of other triphenyltin compounds in soil(SRC). For example, 14C-phenyl ring-labelled triphenyltin acetate is degraded to inorganic tin in soil presumably by biodegradation since carbon dioxide was evolved and the breakdown did not occur in sterile soil(1). Also, triphenyltin fluoride has been observed to degrade in soil faster under aerobic than anaerobic conditions(1).
In rainbow trout, a BCF of about 800 was observed after a 4-day exposure(1). The uptake and elimination rates of radiolabeled triphenyltin hydroxide in guppies were 41 l/kg-day and 0.014/day, giving a BCF (uptake: elimination ratio) of 2900 l/kg (wet weight) during 30 days of exposure(1). For rainbow trout larvae the uptake and elimination rates were 22 l/kg-day and 0.031/day, respectively giving a BCF of 650 ml/g after 4 days; the lower BCF in the trout than the guppies being a result of the higher elimination rate. Since equilibrium was not reached, the bioconcentration factor was underestimated. The log BCFs of triphenyltin in crucian carp obtained in a 7-day experiment were 1.70 (muscle), 1.70 (vertebra); 2.05 (liver); and 1.49 (kidney)(2). In studies in which the bioaccumulation and elimination of triphentyltin in Red Sea bream (Pagrus major) was by direct uptake from water, from diet, and from both simultaneously, about a quarter of the bioaccumulation was due to dietary uptake(3). The bioaccumulation factor was 0.257(3). The elimination rate was 0.020/day and was independent of the source of uptake, water or diet. Bioaccumulation was also independent of the form of triphenyltin in the diet(3). Minnow (Phoxinus phoxinus) embryos/larvae and freshly hatched larvae were exposed to triphenyltin chloride in Lake Lucerne, Switzerland water at 16 deg C(4). The BCF for embryo larvae was 530 at the end of a 192 hr uptake period. Newly hatched larvae had BCFs of 457 and 930 after 96 and 144 hours. At this time the BCF had not reached a plateau so the actual BCF was higher(4). While uptake of triphenyltin from water was rapid, elimination was absent during a 96-hr depuration period. The concn of the metabolites monophenyltin and diphenyltin were very low(4). According to a classification scheme(5), these BCF values suggest the potential for bioconcentration in aquatic organisms is high(SRC).
The Koc for triphenyltin hydroxide is 2,000(SRC), using a measured log Kow of 3.53(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that triphenyltin hydroxide is expected to have low mobility in soil(SRC). If triphenyltin hydroxide is released to soil, it either exists as, or is rapidly converted to oxides, hydroxides, carbonates or hydrated cations(4). Oxides, hydroxides, carbonates or cations are not expected to leach through soil into groundwater(SRC). In a laboratory soil leaching study, triphenyltins were strongly attached to soil(5). This also suggests that triphenyltins (such as triphenyltin hydroxide) may be expected to have low mobility in soil(SRC). The Freundlich parameters, log k and 1/n, for triphenyltin to sediment were 1.81 and 0.793, respectively(6).
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: UN3019 (For reference only, please check.)
IMDG: UN3019 (For reference only, please check.)
IATA: UN3019 (For reference only, please check.)
ADR/RID: ORGANOTIN PESTICIDE, LIQUID, TOXIC, FLAMMABLE, flash point not less than 23 °C (For reference only, please check.)
IMDG: ORGANOTIN PESTICIDE, LIQUID, TOXIC, FLAMMABLE, flash point not less than 23 °C (For reference only, please check.)
IATA: ORGANOTIN PESTICIDE, LIQUID, TOXIC, FLAMMABLE, flash point not less than 23 °C (For reference only, please check.)
ADR/RID: 6.1 (For reference only, please check.)
IMDG: 6.1 (For reference only, please check.)
IATA: 6.1 (For reference only, please check.)
ADR/RID: I (For reference only, please check.)
IMDG: I (For reference only, please check.)
IATA: I (For reference only, please check.)
ADR/RID: Yes
IMDG: Yes
IATA: Yes
no data available
no data available
Carrier solvents used in commercial formulations may change physical and toxicological properties.Do NOT take working clothes home.
The information in this MSDS is only applicable to the specified product, unless otherwise specified, it is not applicable to the mixture of this product and other substances. This MSDS only provides information on the safety of the product for those who have received the appropriate professional training for the user of the product. Users of this MSDS must make independent judgments on the applicability of this SDS. The authors of this MSDS will not be held responsible for any harm caused by the use of this MSDS.