TANGO AUTO DISHWASH
Chemwatch Independent Material Safety Data Sheet
Issue Date: 29-Jan-2010
TANGO AUTO DISHWASH
Powder for automatic dishwashers.
Company: Benji Distributors Pty Ltd Address: 17 Grandview Pde Moolap VIC, 3221 Australia Telephone: +61 3 5248 1469 Fax: +61 3 5248 6696
HAZARDOUS SUBSTANCE. NON-DANGEROUS GOODS. According to NOHSC Criteria, and ADG Code.
|SCALE: Min/Nil=0 Low=1 Moderate=2 High=3 Extreme=4|
|■ Harmful by inhalation and if swallowed.||■ Keep locked up.|
|■ Contact with acids liberates toxic gas.||■ Use only in well ventilated areas.|
|■ Causes burns.||■ Keep container in a well ventilated place.|
|■ Risk of serious damage to eyes.||■ Avoid exposure - obtain special instructions before use.|
|■ Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.||■ To clean the floor and all objects contaminated by this material, use water.|
|■ Cumulative effects may result following exposure*.||■ This material and its container must be disposed of in a safe way.|
|■ May be harmful to the foetus/ embryo*.||■ Take off immediately all contaminated clothing.|
|* (limited evidence).||■ In case of accident or if you feel unwell IMMEDIATELY contact Doctor or Poisons Information Centre (show label if possible).|
|■ Use appropriate container to avoid environmental contamination.|
|■ Avoid release to the environment. Refer to special instructions/Safety data sheets.|
· For advice, contact a Poisons Information Centre or a doctor at once.
· Urgent hospital treatment is likely to be needed.
· If swallowed do NOT induce vomiting.
· If vomiting occurs, lean patient forward or place on left side (head-down position, if possible) to maintain open airway and prevent aspiration.
■ If this product comes in contact with the eyes:
· Immediately hold eyelids apart and flush the eye continuously with running water.
· Ensure complete irrigation of the eye by keeping eyelids apart and away from eye and moving the eyelids by occasionally lifting the upper and lower lids.
· Continue flushing until advised to stop by the Poisons Information Centre or a doctor, or for at least 15 minutes.
· Transport to hospital or doctor without delay.
■ If skin or hair contact occurs:
· Immediately flush body and clothes with large amounts of water, using safety shower if available.
· Quickly remove all contaminated clothing, including footwear.
· Wash skin and hair with running water. Continue flushing with water until advised to stop by the Poisons Information Centre.
· Transport to hospital, or doctor.
· If dust is inhaled, remove from contaminated area.
· Encourage patient to blow nose to ensure clear breathing passages.
· Ask patient to rinse mouth with water but to not drink water.
· Seek immediate medical attention.
· If fumes or combustion products are inhaled remove from contaminated area.
· Lay patient down. Keep warm and rested.
· Prostheses such as false teeth, which may block airway, should be removed, where possible, prior to initiating first aid procedures.
· Apply artificial respiration if not breathing, preferably with a demand valve resuscitator, bag-valve mask device, or pocket mask as trained. Perform CPR if necessary.
■ Treat symptomatically. For acute or short- term repeated exposures to highly alkaline materials: · Respiratory stress is uncommon but present occasionally because of soft tissue edema. · Unless endotracheal intubation can be accomplished under direct vision, cricothyroidotomy or tracheotomy may be necessary. · Oxygen is given as indicated. · The presence of shock suggests perforation and mandates an intravenous line and fluid administration.
· Water spray or fog. · Foam. · Dry chemical powder. · BCF (where regulations permit).
· Alert Fire Brigade and tell them location and nature of hazard. · Wear breathing apparatus plus protective gloves for fire only. · Prevent, by any means available, spillage from entering drains or water courses. · Use fire fighting procedures suitable for surrounding area.
· Solid which exhibits difficult combustion or is difficult to ignite. · Avoid generating dust, particularly clouds of dust in a confined or unventilated space as dusts may form an explosive mixture with air, and any source of ignition, i.e. flame or spark, will cause fire or explosion. · Dust clouds generated by the fine grinding of the solid are a particular hazard; accumulations of fine dust (420 micron or less) may burn rapidly and fiercely if ignited; once initiated larger particles up to 1400 microns diameter will contribute to the propagation of an explosion. · A dust explosion may release of large quantities of gaseous products; this in turn creates a subsequent pressure rise of explosive force capable of damaging plant and buildings and injuring people. Decomposition may produce toxic fumes of: carbon dioxide (CO2), metal oxides, other pyrolysis products typical of burning organic material.
· Avoid contamination with oxidising agents i.e. nitrates, oxidising acids, chlorine bleaches, pool chlorine etc. as ignition may result.
Gloves, boots (chemical resistant).
■ Environmental hazard - contain spillage. · Remove all ignition sources. · Clean up all spills immediately. · Avoid contact with skin and eyes. · Control personal contact by using protective equipment.
■ Environmental hazard - contain spillage. Moderate hazard. · CAUTION: Advise personnel in area. · Alert Emergency Services and tell them location and nature of hazard. · Control personal contact by wearing protective clothing. · Prevent, by any means available, spillage from entering drains or water courses.
Personal Protective Equipment advice is contained in Section 8 of the MSDS.
· Avoid all personal contact, including inhalation.
· Wear protective clothing when risk of exposure occurs.
· Use in a well-ventilated area.
· Prevent concentration in hollows and sumps.
· Polyethylene or polypropylene container.
· Check all containers are clearly labelled and free from leaks.
· Contact with acids produces toxic fumes.
· In presence of moisture, the material is corrosive to aluminium, zinc and tin producing highly flammable hydrogen gas.
· Phosphates are incompatible with oxidising and reducing agents.
· Phosphates are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides.
· Partial oxidation of phosphates by oxidizing agents may result in the release of toxic phosphorus oxides.
· Avoid reaction with oxidising agents.
· Store in original containers.
· Keep containers securely sealed.
· Store in a cool, dry area protected from environmental extremes.
· Store away from incompatible materials and foodstuff containers.
|Source||Material||Peak ppm||Peak mg/m³|
|Australia Exposure Standards||sodium dichloroisocyanurate (Chlorine)||1||3|
The following materials had no OELs on our records
|• sodium carbonate:||CAS:497-19-8|
|• sodium metasilicate:||CAS:1344-09-8|
|• sodium tripolyphosphate:||CAS:7758-29-4 CAS:15091-98-2|
Type AB- P Filter of sufficient capacity
· Chemical goggles. · Full face shield may be required for supplementary but never for primary protection of eyes · Contact lenses may pose a special hazard; soft contact lenses may absorb and concentrate irritants. A written policy document, describing the wearing of lens or restrictions on use, should be created for each workplace or task. This should include a review of lens absorption and adsorption for the class of chemicals in use and an account of injury experience. Medical and first- aid personnel should be trained in their removal and suitable equipment should be readily available. In the event of chemical exposure, begin eye irrigation immediately and remove contact lens as soon as practicable. Lens should be removed at the first signs of eye redness or irritation - lens should be removed in a clean environment only after workers have washed hands thoroughly. [CDC NIOSH Current Intelligence Bulletin 59].
· Wear chemical protective gloves, eg. PVC. · Wear safety footwear or safety gumboots, eg. Rubber.
· Overalls. · P.V.C. apron. · Barrier cream. · Skin cleansing cream. The local concentration of material, quantity and conditions of use determine the type of personal protective equipment required. For further information consult site specific CHEMWATCH data (if available), or your Occupational Health and Safety Advisor.
· Local exhaust ventilation is required where solids are handled as powders or crystals; even when particulates are relatively large, a certain proportion will be powdered by mutual friction. · If in spite of local exhaust an adverse concentration of the substance in air could occur, respiratory protection should be considered. Such protection might consist of: (a): particle dust respirators, if necessary, combined with an absorption cartridge; (b): filter respirators with absorption cartridge or canister of the right type; (c): fresh- air hoods or masks. Air contaminants generated in the workplace possess varying " escape" velocities which, in turn, determine the " capture velocities" of fresh circulating air required to effectively remove the contaminant.
White powder; mixes with water.
Mixes with water.
Contact with acids liberates toxic gas.
|State||Divided Solid||Molecular Weight||Not Available|
|Melting Range (ºC)||Not Available||Viscosity||Not Available|
|Boiling Range (ºC)||Not Available||Solubility in water (g/L)||Miscible|
|Flash Point (ºC)||Not Applicable||pH (1% solution)||10.6-11.0|
|Decomposition Temp (ºC)||Not Available||pH (as supplied)||Not Available|
|Autoignition Temp (ºC)||Not Available||Vapour Pressure (kPa)||Not Available|
|Upper Explosive Limit (%)||Not Available||Specific Gravity (water=1)||Not Available|
|Lower Explosive Limit (%)||Not Available||Relative Vapour Density (air=1)||Not Available|
|Volatile Component (%vol)||Not Available||Evaporation Rate||Not Available|
· Presence of incompatible materials.
· Product is considered stable.
· Hazardous polymerisation will not occur.
For incompatible materials - refer to Section 7 - Handling and Storage.
|ACUTE HEALTH EFFECTS||CHRONIC HEALTH EFFECTS|
|■ Causes burns.||■ May be harmful to the foetus/ embryo*.|
|■ Risk of serious damage to eyes.||■ Cumulative effects may result following exposure*.|
|■ Harmful by inhalation and if swallowed.||■ * (limited evidence).|
■ unless otherwise specified data extracted from RTECS - Register of Toxic Effects of Chemical Substances. ■ Not available. Refer to individual constituents. ■ Asthma- like symptoms may continue for months or even years after exposure to the material ceases. This may be due to a non- allergenic condition known as reactive airways dysfunction syndrome (RADS) which can occur following exposure to high levels of highly irritating compound. SODIUM METASILICATE: SODIUM CARBONATE: ■ The material may cause skin irritation after prolonged or repeated exposure and may produce a contact dermatitis (nonallergic). This form of dermatitis is often characterised by skin redness (erythema) and swelling epidermis. SODIUM CARBONATE:
|Oral (rat) LD50: 4090 mg/kg||Skin (rabbit): 500 mg/24h Mild|
|Inhalation (rat) LC50: 2300 mg/m³/2h||Eye (rabbit): 100 mg/24h Moderate|
|Oral (Rat) LD50: 2800 mg/kg *||Eye (rabbit): 100 mg/30s Mild|
|Dermal (Rat) LD50: >2000 mg/kg *||Eye (rabbit): 50 mg SEVERE|
|Oral (Human) LD: 714 mg/kg|
|Oral (Mouse) LD50: 6600 mg/kg|
|Inhalation (Mouse) LC50: 1200 mg/m³/2h|
|Intraperitoneal (Mouse) LD50: 117 mg/kg|
|Inhalation (Guinea pig) LC50: 800 mg/m³/2h|
|Subcutaneous (Mouse) LD50: 2210 mg/kg|
|Oral (rat) LD50: 1153 mg/kg||Skin (human): 250 mg/24h SEVERE|
|Skin (rabbit): 250 mg/24h SEVERE|
|Oral (Rat) LD50: 5190 mg/kg||Nil Reported|
|Dermal (Rabbit) LD50: >3160 mg/kg *|
|Oral (human) LDLo: 3570 mg/kg||Eye (rabbit): 10 mg/24hr-Moderate|
|Dermal (rabbit) LD50: 6000 mg/kg||Skin (rabbit) : SEVERE *|
|Inhalation (human) LCLo: 500 ppm/5 minutes|
|Inhalation (rat) LC50: 293 ppm/1 hour|
|Oral (Human) LD: 3570 mg/kg|
|Oral (Rat) LD50: 1420 mg/kg|
|Oral (Rabbit) LD: 2500 mg/kg|
|Oral (Rat) LD50: 700 mg/kg *|
Toxic to aquatic organisms, may cause long- term adverse effects in the aquatic environment. Avoid release to the environment. Refer to special instructions/ safety data sheets.
|Ingredient||Persistence: Water/Soil||Persistence: Air||Bioaccumulation||Mobility|
· Containers may still present a chemical hazard/ danger when empty.
· Return to supplier for reuse/ recycling if possible.
· If container can not be cleaned sufficiently well to ensure that residuals do not remain or if the container cannot be used to store the same product, then puncture containers, to prevent re-use, and bury at an authorised landfill.
· Where possible retain label warnings and MSDS and observe all notices pertaining to the product.
· Recycle wherever possible.
· Consult manufacturer for recycling options or consult local or regional waste management authority for disposal if no suitable treatment or disposal facility can be identified.
· Dispose of by: burial in a land-fill specifically licenced to accept chemical and / or pharmaceutical wastes or Incineration in a licenced apparatus (after admixture with suitable combustible material)
· Decontaminate empty containers. Observe all label safeguards until containers are cleaned and destroyed.
None (ADG7) NOT REGULATED FOR TRANSPORT OF DANGEROUS GOODS: ADG7, UN, IATA, IMDG
POISONS SCHEDULE None
Regulations for ingredients
"Australia Hazardous Substances","Australia High Volume Industrial Chemical List (HVICL)","Australia Inventory of Chemical Substances (AICS)","CODEX General Standard for Food Additives (GSFA) - Additives Permitted for Use in Food in General, Unless Otherwise Specified, in Accordance with GMP","GESAMP/EHS Composite List - GESAMP Hazard Profiles","IMO IBC Code Chapter 17: Summary of minimum requirements","International Council of Chemical Associations (ICCA) - High Production Volume List","OECD Representative List of High Production Volume (HPV) Chemicals"
"Australia High Volume Industrial Chemical List (HVICL)","Australia Inventory of Chemical Substances (AICS)","GESAMP/EHS Composite List - GESAMP Hazard Profiles","IMO IBC Code Chapter 17: Summary of minimum requirements","IMO MARPOL 73/78 (Annex II) - List of Noxious Liquid Substances Carried in Bulk","International Council of Chemical Associations (ICCA) - High Production Volume List","OECD Representative List of High Production Volume (HPV) Chemicals"
"Australia High Volume Industrial Chemical List (HVICL)","Australia Inventory of Chemical Substances (AICS)","OECD Representative List of High Production Volume (HPV) Chemicals"
"Australia Hazardous Substances","Australia Inventory of Chemical Substances (AICS)","Australia Standard for the Uniform Scheduling of Drugs and Poisons (SUSDP) - Appendix E (Part 2)","International Air Transport Association (IATA) Dangerous Goods Regulations","International Council of Chemical Associations (ICCA) - High Production Volume List","OECD Representative List of High Production Volume (HPV) Chemicals"
|sodium tripolyphosphate||7758-29-4, 15091-98-2|
17 Grandview Parade
■ Classification of the preparation and its individual components has drawn on official and authoritative sources as well as independent review by the Chemwatch Classification committee using available literature references.
A list of reference resources used to assist the committee may be found at:
■ The (M)SDS is a Hazard Communication tool and should be used to assist in the Risk Assessment. Many factors determine whether the reported Hazards are Risks in the workplace or other settings.
This document is copyright. Apart from any fair dealing for the purposes of private study, research, review or
criticism, as permitted under the Copyright Act, no part may be reproduced by any process without written
permission from CHEMWATCH. TEL (+61 3) 9572 4700.
Issue Date: 29-Jan-2010
Print Date: 15-Nov-2010
This is the end of the MSDS.