柠檬酸舒芬太尼

柠檬酸舒芬太尼名称

[ CAS 号 ]:
60561-17-3

[ 中文名 ]:
柠檬酸舒芬太尼

[ 英文名 ]:
sufentanil citrate

[英文别名 ]:

柠檬酸舒芬太尼物理化学性质

[ 沸点 ]:
493.1ºC at 760 mmHg

[ 熔点 ]:
96.6ºC

[ 分子式 ]:
C28H38N2O9S

[ 分子量 ]:
578.67400

[ 闪点 ]:
252ºC

[ 精确质量 ]:
578.23000

[ PSA ]:
193.15000

[ LogP ]:
2.90420

[ 外观性状 ]:
white to beige

[ 储存条件 ]:
-20°C Freezer

[ 水溶解性 ]:
H2O: soluble1mg/mL, clear

柠檬酸舒芬太尼MSDS

柠檬酸舒芬太尼毒性和生态

CHEMICAL IDENTIFICATION

RTECS NUMBER :
UE5295000
CHEMICAL NAME :
Propionanilide, N-(4-(methoxymethyl)-1-(2-(2-thienyl)ethyl)-4-piperid yl)-, citrate
CAS REGISTRY NUMBER :
60561-17-3
LAST UPDATED :
199009
DATA ITEMS CITED :
9
MOLECULAR FORMULA :
C22-H30-N2-O2-S.C6-H8-O7
MOLECULAR WEIGHT :
578.74
WISWESSER LINE NOTATION :
T6NTJ DNR&V2 D1O1 A2- BT5SJ &QV1U1VQ -T

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Human - woman
DOSE/DURATION :
1200 ng/kg
TOXIC EFFECTS :
Behavioral - convulsions or effect on seizure threshold
REFERENCE :
AACRAT Anesthesia and Analgesia (New York). (Elsevier Science Pub. Co., Inc., 52 Vanderbilt Ave., New York, NY 10017) V.36- 1957- Volume(issue)/page/year: 66,91,1987
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Human - man
DOSE/DURATION :
606 ng/kg/5M-C
TOXIC EFFECTS :
Behavioral - convulsions or effect on seizure threshold
REFERENCE :
AACRAT Anesthesia and Analgesia (New York). (Elsevier Science Pub. Co., Inc., 52 Vanderbilt Ave., New York, NY 10017) V.36- 1957- Volume(issue)/page/year: 66,91,1987
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Human - woman
DOSE/DURATION :
23 ug/kg/10M-C
TOXIC EFFECTS :
Vascular - BP lowering not characterized in autonomic section
REFERENCE :
AACRAT Anesthesia and Analgesia (New York). (Elsevier Science Pub. Co., Inc., 52 Vanderbilt Ave., New York, NY 10017) V.36- 1957- Volume(issue)/page/year: 65,703,1986
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Human - man
DOSE/DURATION :
2777 ng/kg/3M-C
TOXIC EFFECTS :
Vascular - BP lowering not characterized in autonomic section
REFERENCE :
AACRAT Anesthesia and Analgesia (New York). (Elsevier Science Pub. Co., Inc., 52 Vanderbilt Ave., New York, NY 10017) V.36- 1957- Volume(issue)/page/year: 65,703,1986
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraspinal
SPECIES OBSERVED :
Human - woman
DOSE/DURATION :
1 ug/kg/20H-I
TOXIC EFFECTS :
Lungs, Thorax, or Respiration - dyspnea
REFERENCE :
ANASAB Anaesthesia. (Academic Press Inc. Ltd., 24-28 Oval Rd., London NW1 7DX, UK) V.1- 1946- Volume(issue)/page/year: 42,665,1987
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
17900 ug/kg
TOXIC EFFECTS :
Behavioral - analgesia
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 26,1548,1976
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
18700 ug/kg
TOXIC EFFECTS :
Behavioral - convulsions or effect on seizure threshold
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 26,1551,1976
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
14100 ug/kg
TOXIC EFFECTS :
Peripheral Nerve and Sensation - flaccid paralysis without anesthesia (usually neuromuscular blockage) Behavioral - altered sleep time (including change in righting reflex) Behavioral - convulsions or effect on seizure threshold
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 26,1551,1976
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - guinea pig
DOSE/DURATION :
11800 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
MDACAP Medicamentos de Actualidad. (J.R. Prous, S.A., Apartado de Correos 540, 08080 Barcelona, Spain) V.1- 1965- Volume(issue)/page/year: 21,210,1985
点击显示

柠檬酸舒芬太尼安全信息

[ 符号 ]:

GHS02, GHS06, GHS08

[ 信号词 ]:
Danger

[ 危害声明 ]:
H225-H301 + H311 + H331-H370

[ 警示性声明 ]:
P210-P260-P280-P301 + P310-P311

[ 危害码 (欧洲) ]:
T+,T,F

[ 风险声明 (欧洲) ]:
26/27/28-39/23/24/25-23/24/25-11

[ 安全声明 (欧洲) ]:
26-27-28-36/37/39-45-36/37-16-7

[ 危险品运输编码 ]:
UN 3249

[ 包装等级 ]:
III

[ 危险类别 ]:
6.1(b)

柠檬酸舒芬太尼合成路线

柠檬酸舒芬太尼上下游产品

柠檬酸舒芬太尼上游产品

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柠檬酸舒芬太尼文献

Sufentanil citrate: a new opioid analgesic for use in anesthesia.

Pharmacotherapy 4(1) , 11-9, (1984)

Sufentanil citrate is a potent analogue of fentanyl that has been evaluated primarily for use in opioid anesthesia. It is a pure mu receptor agonist and produces the typical spectrum of opioid effects...

Criteria for use of fentanyl citrate, sufentanil citrate, and alfentanil hydrochloride.

Clin. Pharm. 10(8) , 635-7, (1991)

Influence of intensive care treatment on the protein binding of sufentanil and hydromorphone during pain therapy in postoperative cardiac surgery patients.

Br. J. Anaesth. 113(4) , 677-87, (2014)

Our objective was to evaluate the effect of intensive care treatment on the protein binding of sufentanil and hydromorphone in cardiac surgery patients during postoperative analgesia using a target-co...


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