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WATTYL LINSEED OIL MSDS报告[下载][中文版]

Section 1 - CHEMICAL PRODUCT AND COMPANY IDENTIFICATION

PRODUCT NAME

WATTYL LINSEED OIL

NFPA

Flammability 1
Toxicity 0
Body Contact 2
Reactivity 2
Chronic 2
SCALE: Min/Nil=0 Low=1 Moderate=2 High=3 Extreme=4

PRODUCT USE

Timber treatment. HAZARD Rags soaked in linseed oil autoxidise, may generate heat,
smoulder and burn. Oily rags should be collected and immersed in water.

SYNONYMS

"linseed oil", "timber treatment"

Section 2 - HAZARDS IDENTIFICATION

CANADIAN WHMIS SYMBOLS

EMERGENCY OVERVIEW

RISK

Contact with combustible material may cause fire.

POTENTIAL HEALTH EFFECTS

ACUTE HEALTH EFFECTS

SWALLOWED

  The material has NOT been classified as "harmful by ingestion". This is because of the lack of corroborating animal or human evidence. The material may still be damaging to the health of the individual, following ingestion, especially where pre-existing organ (e.g. liver, kidney) damage is evident. Present definitions of harmful or toxic substances are generally based on doses producing mortality (death) rather than those producing morbidity (disease, ill-health). Gastrointestinal tract discomfort may produce nausea and vomiting. In an occupational setting however, unintentional ingestion is not thought to be cause for concern.  

EYE

  Although the liquid is not thought to be an irritant, direct contact with the eye may produce transient discomfort characterized by tearing or conjunctival redness (as with windburn).  

SKIN

  There is some evidence to suggest that the material may cause moderate inflammation of the skin either following direct contact or after a delay of some time. Repeated exposure can cause contact dermatitis which is characterized by redness, swelling and blistering.  Skin contact is not thought to have harmful health effects, however the material may still produce health damage following entry through wounds, lesions or abrasions.  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.  

INHALED

  The material is not thought to produce adverse health effects or irritation of the respiratory tract (as classified using animal models). Nevertheless, good hygiene practice requires that exposure be kept to a minimum and that suitable control measures be used in an occupational setting.  Not normally a hazard due to non-volatile nature of product.  

CHRONIC HEALTH EFFECTS

  Limited evidence suggests that repeated or long-term occupational exposure may produce cumulative health effects involving organs or biochemical systems.  There is some evidence to provide a presumption that human exposure to the material may result in impaired fertility on the basis of: some evidence in animal studies of impaired fertility in the absence of toxic effects, or evidence of impaired fertility occurring at around the same dose levels as other toxic effects but which is not a secondary non-  specific consequence of other toxic effects.  Based on experience with animal studies, there is a possibility that exposure to the material may result in toxic effects to the development of the fetus, at levels which do not cause significant toxic effects to the mother.  Glyceryl triesters (triglycerides), following ingestion, are metabolised to monoglycerides, free fatty acids and glycerol, all of which are absorbed in the intestinal mucosa and undergo further metabolism. Little or no acute, subchronic or chronic oral toxicity was seen in animal studies unless levels approached a significant percentage of calorific intake. Subcutaneous injections of tricaprylin in rats over a five-week period caused granulomatous reaction characterised by oil deposits surrounded by macrophages. Diets containing substantial levels of tributyrin produced gastric lesions in rats fed for 3-35 weeks; the irritative effect of the substance was thought to be the cause of tissue damage.  Dermal application was not associated with significant irritation in rabbit skin; ocular exposures were, at most, mildly irritating to rabbit eyes. No evidence of sensitisation or photosensitisation was seen in a guinea pig maximisation test. Most of the genotoxicity test systems were negative. Tricaprylin, trioctanoin and triolein have been used, historically, as vehicles in carcinogenicity testing of other chemicals. In one study, subcutaneous injection of tricaprylin, in newborn mice, produced more tumours in lymphoid tissue than were seen in untreated animals whereas, in another study, subcutaneous or intraperitoneal injection in 4- to 6-week old female mice produced no tumours. Trioctanoin injected subcutaneously in hamster produced no tumours; when injected intraperitoneally in pregnant rats there was an increase in mammary tumours among the off-spring but similar studies in pregnant hamsters and rabbits showed no tumours in the off-spring.  The National Toxicological Program conducted a 2-year study in rats given tricaprylin by gavage. The treatment was associated with a statistically significant dose-related increase in pancreatic acinar cell hyperplasia and adenoma but there were no acinar carcinomas.  Tricaprylin is not teratogenic to mice or rats but some reproductive effects were seen in rabbits. A low level of foetal eye abnormalities and a small percentage of abnormal sperm were reported in mice injected with trioctanoin.  Human and animal exposures to the phytooestrogens (for example the isoflavones, some flavonoids, saponin, coumestans and lignans) can be high because these compounds are found in many foods. Interest in the dietary phytooestrogens derives from their apparent protective effects against cancer, cardiovascular disease and osteoporosis. High levels, over extended periods, may produce toxic effects.However, toxicological studies revealed that when administered in isolated or enriched form or at high doses isoflavones impair the function of the thyroid gland. It cannot be ruled out that this oestrogen-like effect also encourages the onset of breast cancer. Since women are more at risk of developing cancer in any case after menopause, the intake of food supplements with a high isoflavone content may present unexpected risks for this group of consumers.Although phytooestrogens exist as the inactive glycoside in food products, bacterial beta-glycosidases, in the colon, hydrolyse the glycosides to the active aglycones.A common feature of the phytooestrogens is their striking similarity to 17beta-oestrodiol and the synthetic oestrogen, diethylstilboestrol. There is evidence that phytooestrogens may mediate oestrogen-like effects by direct interaction with the oestrogen receptor of cells. Although the hormonal activity of phytooestrogens is two to five orders of magnitude below that of oestradiol, their high concentration in certain plants and their slower metabolic disposition, can lead to tissue levels exceeding those of endogenous oestrogens by a factor of a thousand or more.There is also evidence that phytooestrogens may influence animal and human health by acting as antioxidants and hydrogen peroxide scavengers or by interfering with eicosanoid and cytokine production and cell signalling.Anogenital distance, puberty onset, oestrus cycling, growth, sex-organ weight and hormonal profile are indicators of oestrogen- or anti-oestrogen like activity. Of interest is the finding that low doses of the dietary isoflavone, genistein, taken by pregnant rats produced shorter anogenital distances in the offspring; high doses did not produce this effect. Exposure to a 5% flaxseed diet (high in lignans) during pregnancy and lactation, resulted in the delayed puberty onset in rats (anti-oestrogenic effect). By contrast, a 10% flaxseed diet produced an earlier onset of puberty (an oestrogenic effect), but longer oestrus cycles due to prolonged dioestrus (an antioestrogenic effect).There have been many reports of phytooestrogens disrupting reproductive activity in sheep. Infertility in sheep (so-called "clover disease") has been traced to isoflavone concentrations in clover (up to 5% dry weight). Temporary infertility is attributed to increased embryo mortality and a reduction or cessation in ovulation. Permanent infertility, in sheep, is purported to occur after 3 years of exposure to dietary oestrogenic compounds; this infertility is due to permanent changes in the architecture of the cervix and also changes in the viscoelasticity of the cervical mucous which prevents the transport of sperm through the cervix. In addition to these effects, phytooestrogens exert effects on oestrogen-sensitive tissues such as the mammary gland and female reproductive organs of the ewe. Cattle have also been shown to be sensitive to the oestrogen-like effects of dietary phytooestrogens. Specific observations include swelling of the vulva, discharge of cervical mucous, uterus enlargements and cystic ovaries. Irregular oestrus cycles, including periods of anoestrus, and decreased rates of conception have also been reported. The impact on reproductive activity, by phytooestrogens on humans, is unknown.The recent practice of feeding infants soy-based formula raises issues related to the long-term health effects of exposure during development. It has been recognised, for example, that the practice may be associated with goiter (thyroid enlargement associated with thyroid hormone deficiency) in humans and animals. Soy phytooestrogens inhibit thyroid hormone synthesis at concentrations which occur in infant formula.If sufficient inhibition of iodide uptake by the goiter occurs, formation of thyroid hormones is depressed. These hormones are essential to the regulation of oxygen consumption and metabolism throughout the body. Clinical manifestations of this so-called "hypothyroidism (or athyrea)" include low metabolic rate,  a tendency to gain weight, somnolence, and myxoedema (a relatively hard oedema of the subcutaneous tissue), dryness and loss of hair, low body temperature, hoarseness, muscle weakness, a slow return of the muscle after tendon jerk, and slow mentation. When hypothyroidism occurs in women, early in pregnancy, the foetus is at risk of impaired physical and mental development, the severity of the impairment depending on the degree of hypothyroidism.  
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