Skin sensitization, Category 1
Hazardous to the aquatic environment, short-term (Acute) - Category Acute 1
Hazardous to the aquatic environment, long-term (Chronic) - Category Chronic 1
H317 May cause an allergic skin reaction
H410 Very toxic to aquatic life with long lasting effects
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P272 Contaminated work clothing should not be allowed out of the workplace.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P273 Avoid release to the environment.
P302+P352 IF ON SKIN: Wash with plenty of water/...
P333+P317 If skin irritation or rash occurs: Get medical help.
P321 Specific treatment (see ... on this label).
P362+P364 Take off contaminated clothing and wash it before reuse.
P391 Collect spillage.
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.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth.
SYMPTOMS: Symptoms of exposure to this compound may include allergic contact dermatitis. Skin contact may also lead to sensitization. Eye contact can cause irritation. ACUTE/CHRONIC HAZARDS: This compound may be harmful by inhalation, ingestion or skin absorption. It is very irritating to the eyes. When heated to decomposition or upon contact with acid or acid fumes, it emits highly toxic fumes of carbon monoxide, carbon dioxide, sulfur oxides and nitrogen oxides. (NTP, 1992)
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 as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on 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. Aromatic hydrocarbons and related compounds
Suitable extinguishing media: Use water spray, alchohol-resistant foam, dry chemical or carbon dioxide.
This chemical is combustible. (NTP, 1992)
Use water spray, dry powder, foam, carbon dioxide.
Personal protection: face shield and particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered sealable containers. If appropriate, moisten first to prevent dusting. 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 sealable containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.
Personal precautions, protective equipment and emergency procedure: Use personal protective equipment. Avoid dust formation. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Avoid breathing dust.
NO open flames. PREVENT DISPERSION OF DUST. Closed system, dust explosion-proof electrical equipment and lighting. 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.
Separated from acids.Conditions for safe storage, including any incompatibilities: Keep container tightly closed in a dry and well-ventilated place.
MAK: (inhalable fraction): 4 mg/m3; carcinogen category: 3B; sensitization of skin (SH); pregnancy risk group: C
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.
Protective gloves. Protective clothing.
Use local exhaust or breathing protection.
no data available
Solid. Crystalline.
Yellow.
Disagreeable odor
180 - 182 °C.
64°C/4mmHg
Combustible. Gives off irritating or toxic fumes (or gases) in a fire.
no data available
200 °C.
628°C
no data available
no data available
no data available
less than 1 mg/mL at 66° F (NTP, 1992)
log Pow = 2.42.
< 0 hPa. Temperature:25 °C.
1.42 g/cm3. Temperature:20 °C.
no data available
no data available
Decomposes on burning. This produces toxic and irritating fumes (sulfur oxides, nitrogen oxides). Reacts with acids and acid fumes. This produces toxic and irritating fumes (sulfur oxides, nitrogen oxides).
no data available
2-MERCAPTOBENZOTHIAZOLE is incompatible with strong oxidizing agents. Also incompatible with acids and acid fumes (NTP, 1992).
no data available
on contact with acid or acid fumes it emits toxic /oxides of sulfur and oxides of nitrogen/.
When heated to decomp ... it emits toxic /oxides of sulfur and oxides of nitrogen/.
no data available
no data available
no data available
no data available
Cancer Classification: Group C Possible Human Carcinogen
no data available
The substance may be irritating to the eyes.
Repeated or prolonged contact may cause skin sensitization. See Notes. This substance is probably carcinogenic to humans.
No indication can be given about the rate at which a harmful concentration of this substance in the air is reached.
AEROBIC: Several biodegradation studies with 2-mercaptobenzothiazole using an activated sludge seed inoculum indicate little or no biodegration(1-4). 2-Mercaptobenzothiazole, present at 100 mg/L, reached only 2.5% of its theoretical BOD in 2 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test indicating the compound is not readily biodegradable(1). It has been suggested that at the concentrations used in these studies, 56-100 ppm, 2-mercaptobenzothiazole is toxic to the microorganisms in the sludge(5). A more detailed study indicated that inhibitory effects occur between 20 and 50 ppm of 2-mercaptobenzothiazole(5). When the sludge is well acclimated and the concentrations low enough, 2-mercaptobenzothiazole may completely biodegrade forming 2-benzothiazolesulfonate or dibenzothiazole-2,2-disulfide, depending on conditions(5). In a screening test comparable to OECD Method 301B (CO2 evolution), 2-mercaptobenzothiazole, present at 17-18 mg/L, reached only 1-5% degradation after 35 days of incubation which classified the compound as not inherently biodegradable(6). Another CO2 evolution study determined <1% degradation after 28 days using adapted activated sludge and an initial 2-mercaptobenzothiazole concentration of 23.8 mg/L(6). Partial degradation of 2-mercaptobenzothiazole was found in laboratory-scale fed-batch systems using activated sludge inoculum taken from rubber chemicals wastewater treatment plants(6).
A BCF of <8 was measured in fish for 2-mercaptobenzothiazole(SRC), using carp (Cyprinus carpio) which were exposed over a 6-week period(1). According to a classification scheme(2), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
The Koc of 2-mercaptobenzothiazole was measured as 677, 326 and 1360 in California sandy loam, California clay loam and California sandy soil respectively(1). The Koc of 2-mercaptobenzothiazole was measured as 2130, 3560 and 2590 in three different sediments(1). The Koc of 2-mercaptobenzothiazole was measured as 915, 863, 1429 and 1829 in Drummer silty clay loam, Spinks sandy loam, Ray silt loam and Lintonia sandy loam soil respectively(1). According to a classification scheme(2), these estimated Koc values suggest that 2-mercaptobenzothiazole is expected to have moderate to slight mobility in soil. The pKa of 2-mercaptobenzothiazole is 7.03(1), indicating that this compound will exist partially in anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(3).
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: UN3077 (For reference only, please check.)
IMDG: UN3077 (For reference only, please check.)
IATA: UN3077 (For reference only, please check.)
ADR/RID: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, SOLID, N.O.S. (For reference only, please check.)
IMDG: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, SOLID, N.O.S. (For reference only, please check.)
IATA: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, SOLID, N.O.S. (For reference only, please check.)
ADR/RID: 9 (For reference only, please check.)
IMDG: 9 (For reference only, please check.)
IATA: 9 (For reference only, please check.)
ADR/RID: III (For reference only, please check.)
IMDG: III (For reference only, please check.)
IATA: III (For reference only, please check.)
ADR/RID: Yes
IMDG: Yes
IATA: Yes
no data available
no data available
Do NOT take working clothes home.Isolate contaminated clothing by sealing in a bag or other container.Anyone who has shown skin sensitization due to this substance should avoid all further contact.