10102-20-2O=[Te]([O-])[O-].[Na+].[Na+]VOADVZVYWFSHSM-UHFFFAOYSA-LSodium tellurite appears as white crystals. Used in bacteriology and medicine. (EPA, 1998)
10102-20-2DTXSID2064943Rhombic prism
White powder
greater than or equal to 100 mg/mL at 68 °F (NTP, 1992)
Slightly sol in cold water; sol in hot water
Sodium tellurite appears as white crystals. Used in bacteriology and medicine. (EPA, 1998)
White solid; [Merck Index] White powder; [MSDSonline] Soluble in hot water; [Sax]
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Danger
H300 (17.8%): Fatal if swallowed [Danger Acute toxicity, oral]
P203, P260, P261, P262, P264, P270, P271, P272, P273, P280, P284, P301+P316, P302+P352, P304+P340, P316, P317, P318, P320, P321, P330, P333+P317, P361+P364, P362+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 90 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
The material is both an oral and dermal toxic hazard. The material is toxic by ingestion. Oral ingestion of tellurium compounds is generally regarded as extremely toxic. The probable oral lethal dose is 5-50 mg/kg or between 7 drops and 1 teaspoonful for a 70 kg (150 pound) person. Tellurium compounds are regarded as super toxic for skin exposures. (EPA, 1998)
Highly toxic by ingestion and skin absorption; [CAMEO] Two fatal cases were reported in which sodium tellurite, instead of sodium iodide, was accidentally injected by retrograde pyelography at a dose of about 30 mg/kg; Oral LD50 (rat) = 20 mg/kg; [HSDB] An irritant; [MSDSonline] See Tellurium.
The early and 24 hour effects of 100 simple chemical substances were studied. Albino-guinea-pigs received intracutaneous injections of a test chemical in a standard volume of 0.1 milliliter at time intervals prior to intravenous dye injection. The animals were killed and examined for changes in color distribution due to the dye. The reactions of the substances fell into 4 main categories: (I) no reaction at isotonic concentration; (II) increased vascular permeability with minimal necrosis; (III) increased vascular permeability with necrosis; and (IV) necrosis with minimal effects on vascular permeability. ... Type-II reactions were evoked by magnesium-chloride, calcium-chloride , strontium-chloride, and sodium-arsenite, among others. Sodium-arsenite, sodium-selenite, and sodium-tellurite showed very potent effects on vascular permeability at concentrations as low as 0.3 milligrams per milliliter, with effects occurring within 2 minutes and peaking at 10 hours.
Biological half-time = about 3 weeks; [HSDB]
The whole-body retention of tellurium in rats after IP or IV injection of ... sodium tellurite can be described by a sum of two exponential functions with biological half-times of about 19 hr (42-49% of dose) and 13-15 days (51-58%). After gavage of the same cmpd, a third exponential term (half-time of 3-7 hr) has to be added to account for the rapid elimination of the non-absorbed fraction (70-80%). The whole-body retention model for man assumes a biological half-time of about 3 wk.
As tellurium ranks among the rare non-essential trace elements there is only little known of its intestinal absorption and its metabolic behavior in humans. Data for risk evaluations needed for occupational medicine are based on animal experiments only. In order to investigate the metabolic behaviour of tellurium in man, tellurium in different forms was administered perorally to healthy male human volunteers. It was given as sodium tellurate, sodium tellurite, metallic colloid and intrinsically bound in cress. For the latter, cress was cultivated with tellurium-containing water in order to provide tellurium for ingestion in a form which is more equivalent to foodstuffs. After the administration the urinary excretion of tellurium was determined. Tellurium concentrations were measured in urine samples by means of graphite furnace atomic absorption spectroscopy (GFAAS). From the cumulative tellurium excretion in the first four days after the administration, a percentage intestinal absorption of 25% + or - 10% for soluble tellurium salts can be calculated. The renal tellurium excretion is faster after administration of hexavalent tellurium than after ingestion of the tetravalent form. This can explain the higher toxicity of the tetravalent tellurium compounds found in animal experiments. The introduction of tellurium to cress lowered the intestinal absorption to approximately 15%. For metallic tellurium the fractional intestinal absorption was found to be about 10%.
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Sodium tellurite is a white crystalline solid.
Releases of CERCLA hazardous substances are subject to the release reporting requirement of CERCLA section 103, codified at 40 CFR part 302, in addition to the requirements of 40 CFR part 355. Sodium tellurite is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 500 or 10,000 lbs. Extremely hazardous substances that are solids are subject to either of two threshold planning quantities ... The lower quantity applies only if the solid exists in powdered form and has a particle size less than 100 microns; or is handled in solution or in molten form; or meets the criteria for a National Fire Protection Association (NFPA) rating of 2, 3 or 4 for reactivity. If the solid does not meet any of these criteria, it is subject to the upper ... threshold planning quantity ... .
Signs and Symptoms of Sodium Tellurite Exposure: Signs and symptoms of acute sodium tellurite exposure include the following: headache, metallic taste in mouth, garlic odor on breath, dry mouth and throat, drowsiness, dizziness, and lassitude. Anorexia (loss of appetite), nausea, vomiting, and constipation may be noted. Sodium tellurite may cause dermatitis on skin contact.
SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
TELLURIUM & CMPD MAY BE DISPOSED OF IN SEALED CONTAINERS IN A SECURED SANITARY LANDFILL. /TELLURIUM & CMPD/
0.1 [mg/m3], as Te
8 Hr Time-Weighted Avg (TWA): 0.1 mg/cu m. /Tellurium and compounds (NOS), as Te, excluding hydrogen telluride/
Excursion Limit Recommendation: Excursions in worker exposure levels may exceed 3 times the TLV-TWA for no more than a total of 30 minutes during a work day, and under no circumstances should they exceed 5 times the TLV-TWA, provided that the TLV-TWA is not exceeded. /Tellurium and compounds (NOS), as Te, excluding hydrogen telluride/
0.52 [mg/m3]
3.5 [mg/m3]
21 [mg/m3]
For emergency situations, wear a positive pressure, pressure-demand, full facepiece self-contained breathing apparatus (SCBA) or pressure- demand supplied air respirator with escape SCBA and a fully-encapsulating, chemical resistant suit. (EPA, 1998)
Instrumental neutron activation analysis was used to determine the interactions between the incorporation of selenium (Se) and tellurium (Te) in the liver, kidneys, heart, spleen, lung and small intestine of Balby mice following the intraperitoneal injection of selenocystine and sodium-tellurite in mice injected with salts of cadmium (Cd), arsenic (As), and zinc (Zn). The levels of cobalt (Co), rubidium (Rb), iron (Fe), and mercury (Hg) in the organs of the treated animals were determined. The results demonstrated a competitive interaction between As and Se or Te, and also between Se and Cd. The levels of Co, Fe, Rb, and Hg in the organs examined changed following injection, the corresponding concentrations depending on the injected compounds, although no clear correlations were established between the contents of Co and Fe and the injected compounds. The injection of Se, Te, or Cd resulted in the competitive displacement of Hg, with subsequent increase in the levels of Hg in the small intestine and kidney. Cd had the same effect on Fe, Co, and Rb in the small intestine and kidney, and the levels of Rb also increased following the injection of Se, Zn or As compounds.
/The investigators/ ... described 3 cases of accidental tellurium poisoning where sodium tellurite soln were given instead of sodium iodide during retrograde pyelography. In 2 cases, the dose is about 2 g (approx 30 mg/kg). Two patients died after about 6 hr; death was preceded by vomiting, renal pain, stupor, loss of consciousness, irregular breathing, & cyanosis. Autopsy revealed deposition of black tellurium in the mucosa of the bladder & of the ureter; congestion of lung, liver, spleen, & kidneys; & fatty change of the liver.
A significant incr of chromosome breakage incidence was observed in human leukocytes treated in vitro with sodium tellurite (1.2X10-8 mol/l) ... .
Toxic by ingestion.
Two fatalities occurred after unintentional treatment with 2 g of sodium tellurite by ureteral catheter. The patients died 6 hr post-treatment after experiencing emesis, dyspnea, cyanosis, lapse of consciousness, stupor, & renal pain. Autopsy revealed acute fatty degeneration & edema of the liver.
Cases of sodium tellurite poisoning were presented. A 40 year old male reported to the hospital with left renal pain. The patient was anesthetized and examined with a cystoscope. In what was intended to be a sodium iodide solution was injected and the patient left the hospital in good condition. Three hours later the patient was readmitted suffering great pain. After 2 hours he became cyanotic, dyspneic, and died. Another male, aged 21, had a urinary tract infection treated with calcium mandelate and ammonium chloride. After the injection of what was intended to be sodium-iodide he too developed a mild cyanosis with anemia but recovered within 2 months. A third male, aged 31, also received what was intended to be sodium iodide during the course of cystoscopy. He suffered a progressive cyanosis that caused his death. All three patients had a characteristic garlic odor to their breath. Chemical analysis of the blood revealed that the supposed sodium iodide was actually sodium tellurite. The authors conclude that sodium tellurite causes cyanosis through the formation of sulfhemoglobin.
Long-term ingestion of sodium tellurite ... (1-50 mg/kg body wt, 3-7 months) was accompanied by dark inclusions and degenerative changes in the small intestines of rats and rabbits ... .
Lifetime exposure of rats and of mice to sodium tellurite ... (2 mg tellurium/l drinking water) had no effect on growth and survival rate of males but tellurite reduced the life span of female mice.
Pathomorphological changes in the liver reported as resulting from exposure to tellurium cmpd /rats and rabbits, sodium tellurite, gavage of 5 and 10 mg/kg body wt for 3 months, and of 0.5 mg/kg for 7 months/ range from simple cellular swelling to hydropic and fatty degeneration and cell necrosis.
Impairment of glycogen function, detoxifying functions and of protein metabolism as indicated by dose-related reduction of galactose tolerance, hippuric acid excretion, decr of albumin/globulin ratio in serum, urinary bilirubin excretion, inhibition of cholinesterase, were observed ... /in/ subacute and chronic studies in rats and rabbits, oral admin of sodium tellurite, 0.5-10 mg tellurium/kg body wt.
For more Non-Human Toxicity Excerpts (Complete) data for SODIUM TELLURITE (18 total), please visit the HSDB record page.
Basic treatment: Establish a patent airway. Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if needed. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 ml/kg up to 200 ml of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool ... . Cover skin burns with dry sterile dressings after decontamination ... . /Poison A and B/
Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in respiratory arrest. Positive pressure ventilation techniques with a bag valve mask device may be beneficial. Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start an IV with D5W /SRP: "To keep open", minimal flow rate/. Use lactated Ringer's if signs of hypovolemia are present. Watch for signs of fluid overload. Consider drug therapy for pulmonary edema ... . For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Treat seizures with diazepam (Valium) ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Poison A and B/
LD50 Mouse oral 20 mg/kg
LD50 Rat oral 83 mg/kg
LD50 Rat ip 2400 ug/kg
LD50 Rabbit oral 53,600 ug/kg
Releases of CERCLA hazardous substances are subject to the release reporting requirement of CERCLA section 103, codified at 40 CFR part 302, in addition to the requirements of 40 CFR part 355. Sodium tellurite is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 500 or 10,000 lbs. Extremely hazardous substances that are solids are subject to either of two threshold planning quantities ... The lower quantity applies only if the solid exists in powdered form and has a particle size less than 100 microns; or is handled in solution or in molten form; or meets the criteria for a National Fire Protection Association (NFPA) rating of 2, 3 or 4 for reactivity. If the solid does not meet any of these criteria, it is subject to the upper ... threshold planning quantity ... .
The route of admin (IV, IP ... or orally) does not significantly change the pattern of soft tissue distribution of tellurium given as sodium tellurite or tellurous acid in hydrochloric acid solution. A short-term equilibrium is reached within 1-2 hr; the organs with highest concn incl the kidneys, liver, lung, thyroid, spleen, and the blood. The uptake by skeletal muscles is much slower, and in the long term, tellurium seems to accumulate in the bone.
Injected tellurium (IV and IP as sodium tellurite) is excreted by the rat mainly in urine (14-27% within 24 hr; 33% within one week). Fecal excretion amt to about 6% in 24 hr and 14% in one week. Tellurium is transferred to the intestine by biliary excretion. About 11-16% of IV injected tellurium (as sodium tellurite) was excreted by female dogs within 1 hr, and 23% within 6 days. About 60-80% of ingested sodium tellurite ... was rapidly eliminated by rats and swine in feces.
Gastrointestinal absorption of tellurites is completed within 2 hr and takes place, in rats, mainly in the duodenum and jejunum. Absorption estimates vary from 10- 15% to 25%. In swine, as in sheep, sodium tellurite is absorbed from the colon, but not from the small intestine.
Used in bacteriology; [Hawley]
Bacteriology, medicine
MEDICATION
용도Disodium Tellurite is an effector towards the thyroid hormone system due to it being of a similar group to selenium. Tellurium accumulates in the thyroid gland and influences the zinc thyroid level. I t is also damaging towards DNA in TK6 human lymphoblastoid cells.
일반 설명White crystals. Used in bacteriology and medicine.