替莫碘胺

  • 基本信息
  • 制备方法及用途
  • 物化性质
  • 毒理性
  • 结构与计算化学

替莫碘胺 基本信息

中文名称:
替莫碘胺 
中文别名:
替莫碘胺;
替莫农 
英文名称:
Morpholinium,4-[3-hydroxy-3-phenyl-3-(2-thienyl)propyl]-4-methyl-, iodide (1:1)
英文别名:
3-(4-methylmorpholin-4-ium-4-yl)-1-phenyl-1-thiophen-2-ylpropan-1-ol,iodide;
EINECS 205-616-5;
Tiemonio ioduro [DCIT];
Ioduro de tiemonio [INN-Spanish];
Iodure de tiemonium [INN-French];
tiemonium iodide;
Visceralgine;
Cerfa 114;
Tiemonii iodidum [INN-Latin];
Tiemozyl;
Visceralgin 
CAS No.:
144-12-7
分 子 式:

C18H24NO2S.I

分 子 量:
445.36
精确分子量:
445.05700
PSA:
57.70000
EINECS:
205-616-5
InChI:
The Key: IOFXEUZPIIUQAG-UHFFFAOYSA-M
危险品标志:

 

风险术语:

 

安全术语:
分子结构式:
SDS:
查看

替莫碘胺 制备方法及用途

制备方法

用途:麻醉辅助药(骨骼肌松弛药)

用途简介

用途

用途:麻醉辅助药(骨骼肌松弛药)

替莫碘胺 物化性质

存储条件/存储方法:

密封于干燥阴凉处保存。

稳定性相关:

常温常压下稳定。

替莫碘胺 毒理性

CHEMICAL IDENTIFICATION

RTECS NUMBER :
QF3327500
CHEMICAL NAME :
Morpholinium, 4-(3-hydroxy-3-phenyl-3-(2-thienyl)propyl)-4-methyl-, iodide
CAS REGISTRY NUMBER :
144-12-7
LAST UPDATED :
199012
DATA ITEMS CITED :
8
MOLECULAR FORMULA :
C18-H24-N-O2-S.I
MOLECULAR WEIGHT :
445.39
WISWESSER LINE NOTATION :
T6K DOTJ A1 A2XQR&- BT5SJ &I

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
2295 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 3,390,1969
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
240 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 3,390,1969
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1350 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 3,390,1969
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
30 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. (Heymans Institute of Pharmacology, De Pintelaan 185, B-9000 Ghent, Belgium) V.4- 1898- Volume(issue)/page/year: 141,465,1963
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1800 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 3,390,1969
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
130 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 3,390,1969
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
450 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 3,390,1969
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
30 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
NIIRDN Drugs in Japan (Ethical Drugs). (Yakugyo Jiho Co., Ltd., Tokyo, Japan) Volume(issue)/page/year: 6,865,1982
毒理学数据:

1、急性毒性:大鼠经口LD502295 mg/kg

大鼠腹腔LD50240 mg/kg

大鼠皮下LD501350 mg/kg

大鼠静脉LD5030 mg/kg

小鼠经口LD501800 mg/kg

小鼠腹腔LD50130 mg/kg

小鼠静脉LD5030 mg/kg

小鼠皮下LD50450 mg/kg

生态数据:

三、生态学数据:

通常对水是不危害的,若无政府许可,勿将材料排入周围环境。

替莫碘胺 分子结构与计算化学数据

计算化学数据

1.疏水参数计算参考值(XlogP):无

2.氢键供体数量:1

3.氢键受体数量:4

4.可旋转化学键数量:5

5.互变异构体数量:无

6.拓扑分子极性表面积57.7

7.重原子数量:23

8.表面电荷:0

9.复杂度:353

10.同位素原子数量:0

11.确定原子立构中心数量:0

12.不确定原子立构中心数量:1

13.确定化学键立构中心数量:0

14.不确定化学键立构中心数量:0

15.共价键单元数量:2

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