Section 1 - CHEMICAL PRODUCT AND COMPANY IDENTIFICATION

PRODUCT NAME

JASOL TRANSCLEAN

NFPA

PRODUCT USE

A highly effective, powerful detergent with built- in corrosion inhibitors for the hot or
cold pressure spray- or soak tank cleaning of both ferrous and non- ferrous components.
The low foam action makes it ideal for spray parts washers. For general purpose cleaning
of transmission parts etc., use at a concentration of 0.2 to 0.6% (10g- 30g per 4.5L). For
heavy deposits this may be increased to 1.0% (45g per 4.5L).

Section 2 - HAZARDS IDENTIFICATION

CANADIAN WHMIS SYMBOLS

EMERGENCY OVERVIEW

RISK

Harmful if swallowed.
Toxic by inhalation.
Irritating to eyes, respiratory system and skin.
Toxic to aquatic organisms.

POTENTIAL HEALTH EFFECTS

ACUTE HEALTH EFFECTS

SWALLOWED

  Accidental ingestion of the material may be harmful; animal experiments indicate that ingestion of less than 150 gram may be fatal or may produce serious damage to the health of the individual.  Toxic effects may result from the accidental ingestion of the material; animal experiments indicate that ingestion of less than 40 gram may be fatal or may produce serious damage to the health of the individual.  The material can produce chemical burns within the oral cavity and gastrointestinal tract following ingestion.  In humans, inorganic nitrites produce smooth muscle relaxation, methaemoglobinaemia (MHG) and cyanosis. Fatal poisonings in infants, resulting from ingestion of nitrates in water or spinach, have been reported. The primary effect of nitrite intoxication in animals is MHG whilst secondary effects include vasodilation, relaxation of smooth muscle and lowering of blood pressure. Other nitrite-induced toxic effects include abdominal pain, diarrhoea, atrophied intestinal villi and apoptopic cell death in the intestinal crypts. When sodium nitrite was administered in drinking water for 6 weeks (0.06-1%), mice showed a slight degeneration and spotty necrosis of hepatocytes and haemosiderin deposition in the liver, spleen and lymph nodes, indicating haemolysis. At 2%, mice died within 3 weeks. In rats, subject to the same treatment regime, abnormal blood and spleen colours, due to MHG, were seen in 0.5% and 1.0% treatment groups. Hepatic microsomal lipoperoxidation (as measured by malondialdehyde formation) was increased in male rats given 0.2% sodium nitrite in drinking water. Liver lysosomal enzymes (acid phosphatase aaand cathepsin) and superoxide dismutase activities were also increased. This data suggests that the nitrite stimulates generation of superoxide radicals in the liver causing damage to cellular and subcellular membranes. Decreased plasma vitamin E and greater reduced glutathione-per erythrocyte were also reported in male rats receiving sodium nitrite in drinking water.  

EYE

  This material can cause eye irritation and damage in some persons.  The material can produce chemical burns to the eye following direct contact. Vapors or mists may be extremely irritating.  The material may produce severe irritation to the eye causing pronounced inflammation. Repeated or prolonged exposure to irritants may produce conjunctivitis.  

SKIN

  This material can cause inflammation of the skin oncontact in some persons.  The material can produce chemical burns following direct contactwith the skin.  Skin contact is not thought to produce harmful health effects (as classified using animal models). Systemic harm, however, has been identified following exposure of animals by at least one other route and the material may still produce health damage following entry through wounds, lesions or abrasions. Good hygiene practice requires that exposure be kept to a minimum and that suitable gloves be used in an occupational setting.  Entry into the blood-stream, through, for example, cuts, abrasions or lesions, may produce systemic injury with harmful effects. Examine the skin prior to the use of the material and ensure that any external damage is suitably protected.  The material may cause skin irritation after prolonged or repeated exposure and may produce on contact skin redness, swelling, the production of vesicles, scaling and thickening of the skin.  

INHALED

  If inhaled, this material can irritate the throat andlungs of some persons.  The material is not thought to produce adverse health effects following inhalation (as classified using animal models). Nevertheless, adverse effects have been produced following exposure of animals by at least one other route and good hygiene practice requires that exposure be kept to a minimum and that suitable control measures be used in an occupational setting.  Persons with impaired respiratory function, airway diseases and conditions such as emphysema or chronic bronchitis, may incur further disability if excessive concentrations of particulate are inhaled.  

CHRONIC HEALTH EFFECTS

  Repeated or prolonged exposure to corrosives may result in the erosion of teeth, inflammatory and ulcerative changes in the mouth and necrosis (rarely) of the jaw. Bronchial irritation, with cough, and frequent attacks of bronchial pneumonia may ensue. Gastrointestinal disturbances may also occur. Chronic exposures may result in dermatitis and/or conjunctivitis.  Long term exposure to high dust concentrations may cause changes in lung function i.e. pneumoconiosis; caused by particles less than 0.5 micron penetrating and remaining in the lung. Prime symptom is breathlessness; lung shadows show on X-ray.  Limited evidence suggests that repeated or long-term occupational exposure may produce cumulative health effects involving organs or biochemical systems.  There has been some concern that this material can cause cancer or mutations but there is not enough data to make an assessment.  There is limited evidence that, skin contact with this product is more likely to cause a sensitization reaction in some persons compared to the general population.  Chronic inhalation exposure may result in nasal ulceration and/orperforation of nasal septum.  Oil may contact the skin or be inhaled. Extended exposure can lead to eczema, inflammation of hair follicles, pigmentation of the face and warts on the soles of the feet. There are few systemic effects, but prolonged exposure may lead to a higher incidence of lung scarring.  Exposure to sodium nitrite in drinking water resulted in an increased incidence of epithelial hyperplasia in the forestomach of male and female rats and in the glandular stomach of male mice.There was equivocal evidence of carcinogenic activity of sodium nitrite in female B6C3F1 mice based on the positive trend in the incidences of squamous cell papillomas or carcinomas (combined) of the forestomach. There was no evidence of carcinogenic activity in male and female F344/N rats or B6C3F1 male mice exposed to 750, 1500 or 3000 ppm.  NTP Technical Report Series No. 495, May 2001Under certain conditions, nitrites can react with secondary amines, either alone or in biological systems, to form carcinogenic nitrosamines.Sodium nitrite (60 mg/kg) administered in drinking water to pregnant guinea pigs produced maternal anaemia and increased the incidences of abortion and foetal mortality. Administration of 2000-3000 mg/l sodium nitrite in drinking water, to pregnant rats, produced 30-53% foetal mortality. In rat dams given 0.025-0.5% in feed, sodium nitrite caused an increase in foetal and pup mortality and decreases in pre-weanling body weights.