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disodium;tellurite | 10102-20-2

中文名称
——
中文别名
——
英文名称
disodium;tellurite
英文别名
Na2 Te O3;disodium;trioxidotellanium
disodium;tellurite化学式
CAS
10102-20-2
化学式
Na2O3Te
mdl
——
分子量
221.6
InChiKey
VOADVZVYWFSHSM-UHFFFAOYSA-L
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 溶解度:
    可溶于酸性水溶液(轻微),水(轻微,超声处理)
  • 暴露限值:
    ACGIH: TWA 0.1 mg/m3NIOSH: IDLH 25 mg/m3; TWA 0.1 mg/m3
  • 物理描述:
    Sodium tellurite appears as white crystals. Used in bacteriology and medicine. (EPA, 1998)
  • 颜色/状态:
    Rhombic prism
  • 分解:
    When heated to decomposition it emits toxic fumes of /tellurium & disodium oxide/.
  • 稳定性/保质期:

    可溶于,在空气中受热会转变为碲酸Na2TeO4

计算性质

  • 辛醇/水分配系数(LogP):
    -8.87
  • 重原子数:
    6
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    63.2
  • 氢给体数:
    0
  • 氢受体数:
    3

ADMET

代谢
由于属于稀有的非必需微量元素,人们对其在人体内的肠道吸收和代谢行为知之甚少。职业医学所需的风险评估数据仅基于动物实验。为了研究在人体内的代谢行为,以不同形式给予健康的男性志愿者口服。它以碲酸钠亚碲酸属胶体和固有结合在芥菜中的形式给予。对于后者,使用含培植芥菜,以便以更类似于食品的形式提供以供摄入。给药后,测定了的尿液排泄。使用石墨炉原子吸收光谱法(GFAAS)测量尿样中的浓度。从给药后前四天的累积排泄中,可以计算出可溶性盐的肠道吸收百分比为25% ± 10%。在给予六价后,肾排泄速度比摄入四价形式后更快。这可以解释动物实验中发现的四价化合物毒性更高的现象。将引入芥菜将肠道吸收降低到大约15%。对于,发现其肠道吸收分数约为10%。
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%.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 副作用
神经毒素 - 其他中枢神经系统神经毒素 职业性肝毒素 - 继发性肝毒素:在职业环境中潜在的有毒效应是基于人类摄入或动物实验的中毒案例。 生殖毒素 - 对生殖系统有毒的化学物质,包括后代缺陷以及损伤男性或女性生殖功能。生殖毒性包括发育效应。参见生殖毒性风险评估指南。
Neurotoxin - Other CNS neurotoxin Occupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation. Reproductive Toxin - A chemical that is toxic to the reproductive system, including defects in the progeny and injury to male or female reproductive function. Reproductive toxicity includes developmental effects. See Guidelines for Reproductive Toxicity Risk Assessment.
来源:Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
毒理性
  • 相互作用
仪器中子活化分析被用来确定在小鼠腹腔注射亚硒酸亚碲酸盐后,(Se)和(Te)在Balby小鼠的肝脏、肾脏、心脏、脾脏、肺和小肠中的相互作用。在处理过的动物器官中确定了(Co)、(Rb)、(Fe)和(Hg)的平。结果表明(As)与Se或Te之间存在竞争性相互作用,Se与(Cd)之间也存在类似的相互作用。注射后,检查的器官中的Co、Fe、Rb和Hg平发生了变化,相应的浓度取决于注射的化合物,尽管没有建立Co和Fe含量与注射化合物之间的明确相关性。注射Se、Te或Cd导致Hg的竞争性位移,随后在小肠和肾脏中Hg的平增加。Cd对小肠和肾脏中的Fe、Co和Rb有相同的效果,注射Se、Zn或As化合物后,Rb的平也增加了。
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.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
基本治疗:建立专利气道。如有必要,进行吸痰。观察呼吸不足的迹象,并在需要时辅助通气。通过非循环呼吸面罩以10至15升/分钟的速度给予氧气。监测肺肿,并在必要时进行治疗……。监测休克,并在必要时进行治疗……。预期癫痫发作,并在必要时进行治疗……。对于眼睛污染,立即用冲洗眼睛。在转运过程中,用生理盐连续冲洗每只眼睛……。不要使用催吐剂。对于摄入,如果患者能吞咽、有强烈的干呕反射且不流口,则用冲洗口腔,并给予5毫升/千克,最多200毫升的进行稀释……。在去污后,用干燥的无菌敷料覆盖皮肤烧伤……。/毒药A和B/
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/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
高级治疗:对于昏迷、严重肺肿或呼吸停止的患者,考虑进行口咽或鼻咽插管以控制气道。使用带有气囊面罩的装置进行正压通气技术可能有益。监测心率和必要时治疗心律失常。 ... 开始静脉输液,使用5%葡萄糖/生理盐: "保持开放",最低流速/。如果出现低血容量的迹象,使用乳酸钠林格氏液。注意液体过载的迹象。考虑使用药物治疗肺肿。对于伴有低血容量迹象的低血压,谨慎给予液体。注意液体过载的迹象。使用地西泮安定)治疗癫痫。使用丙美卡因化物协助眼部冲洗。 /毒药A和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/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 医疗监测
如果整个班次工人的平均尿浓度超过0.05毫克/升,应该调查该班次的工作条件。//
If the avg urinary tellurium concn for a whole shift of workers exceeds 0.05 mg/l, the working conditions for the shift should be investigated. /Tellurium/
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
管理路线(静脉注射、皮下注射或口服)对作为亚碲酸碲酸盐酸溶液中给予的的软组织分布模式没有显著影响。在1-2小时内达到短期平衡;包括肾脏、肝脏、肺、甲状腺、脾脏和血液在内的器官浓度最高。骨骼肌的吸收要慢得多,从长远来看,似乎会在骨骼中积累。
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.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
注入的(四价和五价,以亚碲酸形式)主要通过大鼠的尿液排出(24小时内14-27%,一周内33%)。粪便排泄量在24小时内约为6%,在一周内约为14%。通过胆汁排泄转移到肠道中。大约11-16%的静脉注射(以亚碲酸形式)在一小时内由母狗排出,6天内排出23%。大约60-80%摄入的亚碲酸被大鼠和猪快速通过粪便排出。
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.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
肠内吸收化物在2小时内完成,在大鼠中主要发生在十二指肠和空肠。吸收估计从10-15%到25%不等。在猪和羊中,碲化钠是从结肠吸收的,但不是从小肠吸收的。
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.
来源:Hazardous Substances Data Bank (HSDB)

安全信息

  • TSCA:
    Yes
  • 危险等级:
    6.1
  • 安全说明:
    S22,S36/37/39,S45
  • 危险品运输编号:
    UN 3288 6.1/PG 2
  • WGK Germany:
    3
  • 危险类别:
    6.1
  • 危险品标志:
    T
  • 危险类别码:
    R23/24/25
  • RTECS号:
    WY2450000
  • 包装等级:
    II
  • 危险标志:
    GHS06
  • 危险性描述:
    H301 + H311 + H331
  • 危险性防范说明:
    P261,P280,P301 + P310 + P330,P302 + P352 + P312,P304 + P340 + P312,P403 + P233
  • 储存条件:
    密封、阴凉、干燥处保存。

SDS

SDS:55fec47c0d2f8711b23f160d048c805d
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第一部分:化学品名称

制备方法与用途

用途 亚碲酸广泛应用于药物制造、有机合成、细菌学研究、属加工以及电镀试剂。

类别:有毒物品

毒性分级:剧毒

急性毒性:

  • 大鼠口服 LD50: 83 毫克/公斤
  • 小鼠口服 LD50: 20 毫克/公斤

可燃性危险特性:不能燃烧;受热会产生有毒的氧化物和氧化烟雾。

储运特性:

职业标准:

  • 时间加权平均容许浓度(TLV-TWA):0.1 毫克()/立方米
  • 短时间暴露极限(STEL):0.3 毫克()/立方米

反应信息

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文献信息

  • Anet et al., Australian Journal of Scientific Research, Series A: Physical Sciences, 1952, vol. 5, p. 412,415
    作者:Anet et al.
    DOI:——
    日期:——
  • TROFIMOV, B. A.;GUSAROVA, N. K.;TATARINOVA, A. A.;AMOSOVA, S. V., ZH. OBSHCH. XIMII, 1983, 53, N 7, 1680
    作者:TROFIMOV, B. A.、GUSAROVA, N. K.、TATARINOVA, A. A.、AMOSOVA, S. V.
    DOI:——
    日期:——
  • ——
    作者:FUKUOKA YUDZO、 KUBO NAOKI
    DOI:——
    日期:——
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