Eye irritation, Category 2
Warning
H319 Causes serious eye irritation
P264 Wash ... thoroughly after handling.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
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Move the victim into fresh air. If breathing is difficult, give oxygen. If not breathing, give artificial respiration and consult a doctor immediately. Do not use mouth to mouth resuscitation if the victim ingested or inhaled the chemical.
Take off contaminated clothing immediately. Wash off with soap and plenty of water. Consult a doctor.
Rinse with pure water for at least 15 minutes. Consult a doctor.
Rinse mouth with water. Do not induce vomiting. Never give anything by mouth to an unconscious person. Call a doctor or Poison Control Center immediately.
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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
Water spray, dry chemical, carbon dioxide, or foam as appropriate for surrounding fire and materials.
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Wear self-contained breathing apparatus for firefighting if necessary.
HEALTH | 3 | Short exposure could cause serious temporary or moderate residual injury (e.g. liquid hydrogen, sulfuric acid, calcium hypochlorite, hexafluorosilicic acid) | |
FIRE | 0 | Materials that will not burn under typical fire conditions, including intrinsically noncombustible materials such as concrete, stone, and sand. Materials that will not burn in air when exposed to a temperature of 820 °C (1,500 °F) for a period of 5 minutes.(e.g. Carbon tetrachloride) | |
REACT | 0 | Normally stable, even under fire exposure conditions, and is not reactive with water (e.g. helium,N2) | |
SPEC. HAZ. |
Avoid dust formation. Avoid breathing mist, gas or vapours.Avoid contacting with skin and eye. Use personal protective equipment.Wear chemical impermeable gloves. Ensure adequate ventilation.Remove all sources of ignition. Evacuate personnel to safe areas.Keep people away from and upwind of spill/leak.
Prevent further spillage or leakage if it is safe to do so. Do not let the chemical enter drains. Discharge into the environment must be avoided.
Wear approved respiratory protection, chemically compatible gloves and protective clothing. Wipe up spillage or collect spillage using a high efficiency vacuum cleaner. Avoid breathing dust. Place spillage in appropriately labelled container for disposal. Wash spill site.
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.
Store in tight, light-resistant container as defined in the USP-NF. This material should be handled and stored per label instructions to ensure product integrity.
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Ensure adequate ventilation. Handle in accordance with good industrial hygiene and safety practice. Set up emergency exits and the risk-elimination area.
Wear tightly fitting safety goggles with side-shields conforming to EN 166(EU) or NIOSH (US).
Wear fire/flame resistant and impervious clothing. Handle with gloves. Gloves must be inspected prior to use. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it.
If the exposure limits are exceeded, irritation or other symptoms are experienced, use a full-face respirator.
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221°C(lit.)
189°C(lit.)
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84°C(lit.)
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1.344 g/cm3
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This material is assumed to be combustible.
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When heated to decompostion it emits toxic fumes of /hydrogen fluoride and nitrogen oxides/.
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AEROBIC: Norfloxacin, present at 100 ug/L, was not biodegraded in 6 hours using Hong Kong wastewater treatment plant freshwater sewage inoculum (Stanley plant: freshwater sewage; hydraulic retention time 17 hrs; sewage retention time 7 days) in a batch test. Adsorption was the dominant process (adsorption elimination efficiency of 91.6%). Using a saltwater sewage inoculum (Shatin plant: saline sewage; hydraulic retention time 10 hrs; sewage retention time 12 hrs), ciprofloxacin, present at 100 ug/L, was 26.7% biodegraded following an initial adsorption-dominant period of 15 minutes (adsorption elimination efficiency of 60.5%)(1).
An estimated BCF of 3 was calculated in fish for norfloxacin(SRC), using a log Kow of -1.03(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).
A Koc of 61,000 was determined for analogous ciprofloxacin in batch sorption studies using a German soil(1). According to a classification scheme(2), this Koc value suggests that norfloxacin is expected to be immobile in soil. Norfloxacin is an amphoteric compound with pKa values of 6.32 for the carboxylic acid group and 8.47 for the nitrogen on the piperazinyl ring(3); at pHs greater than 6.32, the acid will be primarily dissociated and at pHs less than 8.47, the nitrogen will be primarily protonated(SRC); therefore, norfloxacin will have an ionic charge at any environmental pH(SRC). Norfloxacin, added at 20, 30, 40, 50, 60, and 80 g/kg exhibited Kd values of 5791, 6234, 5382, 4984, 3073, and 1942, respectively, using a Louisiana wastewater treatment wetland soil, Bayou Castine. These values correspond to 91.0, 91.5, 90.0, 89.4, 83.6, and 76.7% sorption, respectively(4).
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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: UN2922 (For reference only, please check.)
IMDG: UN2922 (For reference only, please check.)
IATA: UN2922 (For reference only, please check.)
ADR/RID: CORROSIVE LIQUID, TOXIC, N.O.S. (For reference only, please check.)
IMDG: CORROSIVE LIQUID, TOXIC, N.O.S. (For reference only, please check.)
IATA: CORROSIVE LIQUID, TOXIC, N.O.S. (For reference only, please check.)
ADR/RID: 8 (For reference only, please check.)
IMDG: 8 (For reference only, please check.)
IATA: 8 (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: No
IMDG: No
IATA: No
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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.