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こはく酸 コリン クロリド

Succinylcholine Chloride

HCID 230349
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基本情報名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
71-27-2
標準SMILES
C[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)C.[Cl-]
分子式
C14H30Cl2N2O4
平均分子量
361.3 g/mol

名称と識別子

優先名称
Succinylcholine Chloride
現地名
こはく酸 コリン クロリド
英語名
Succinylcholine Chloride
分子式
C14H30Cl2N2O4
分子量
361.3

名称と別名

こはく酸 コリン クロリド塩化スキサメトニウムアネクチン2,2'-[(1,4-ジオキソ-1,4-ブタン-ジイル)ビス(オキシ)]ビス(N,N,N-トリメチルエタンアミニウム)·2クロリドサクシニルコリンクロライドミオプレギンスクシニルコリンクロリドスキサメトニウムジクロリドスキサメトニウムクロリドサクシンスクシニルコリンジクロリドリステノン
名称をさらに表示
スコリン2,2'-[(1,4-ジオキソ-1,4-ブタンジイル)ビス(オキシ)]ビス[N,N,N-トリメチルエタンアミニウム]·ジクロリドパントラックススクシニルコリンクロリド二水和物塩化サクシニルコリンSUXAMETHONIUM CHLORIDEAnectineDITILINskolinmidarinepantolaxLYSTHENONlysthenonemyoplegineSUCCICURAN

データベース識別子

CAS
71-27-2
PubChem CID
230349

物性

物理化学的性質

融点
164 °C · 164 °C
貯蔵温度
Refrigerator
溶解性
Methanol (Slightly), Water (Slightly)
外見
Solid
色
White to Off-White
Merck
8875 · 8875
安定性
安定。可燃性。強力な酸化剤とは相容れない。
CAS データベース
71 · 71-27-2(CAS DataBase Reference)
EPAの化学物質情報
Succinylcholine chloride (71-27-2)
化学的性質 · 1 件

化学的特性Succinylcholine chloride is a white, odorless, slightly bitter powder and very soluble in water. The drug is unstable in alkaline solutions but relatively stable in acid solutions, depending upon the concentration of the solution and the storage temperature. Solutions of succinylcholine chloride should be stored under refrigeration to preserve potency.

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

安全データ

rtecs
GA2360000
ridadr
3249
毒性
LD50 i.v. in mice: 0.45 mg/kg (Anttila, Ertama)
safety_code
7/8
hazard_class
6.1(b)
packing_group
III

化学と産業

応用分野 · 3 件

説明Succinylcholine chloride is a potent relaxant of voluntary striated muscle but has little direct effect on smooth muscle. It has no anesthetic or pain-obliterating properties; therefore, immobilized animals remain completely conscious although unable to move. The duration of effect is quite brief because succinylcholine is rapidly destroyed by non-specific cholinesterases in the blood plasma and liver. Immobilization lasts five to 12 minutes in man and horses and somewhat longer in other species,with ruminants generally requiring longest recovery periods (Stowe et al. 1958).Since the discovery of its curariform properties in 1949, succinylcholine has been widely used for immobilization of animals and in human surgical procedures. Several workers have used succinylcholine on bears (Black 1958, Knudsen 1959, Craighead et al. 1960, Troyer et al. 1961,Hornocker 1962, Mundy 1963,Pearson et al. 1968, Jonkel and Cowan 1971 and Mundy and Flook 1973).Succinylcholine chloride is indicated as an adjunct to general anesthesia, to facilitate tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation.

使用A neuromuscular blocking agent. Muscle relaxant (skeletal).

一般的な説明Succinylcholine chloride,choline chloride succinate (2:1) (Anectine, Sucostrin),is a white, odorless, crystalline substance that is freely solublein water to give solutions with a pH of about 4. It isstable in acidic solutions but unstable in alkali. Aqueous solutionsshould be refrigerated to ensure stability.Succinylcholine chloride is characterized by a very shortduration of action and a quick recovery because of its rapidhydrolysis after injection. It brings about the typical muscularparalysis caused by blocking nervous transmission at themyoneural junction. Large doses may cause temporary respiratorydepression, as with similar agents. Its action, in contrastwith that of (1)-tubocurarine, is not antagonized byneostigmine, physostigmine, or edrophonium chloride.These anticholinesterase drugs actually prolong the action ofsuccinylcholine chloride, which suggests that the drug isprobably hydrolyzed by cholinesterases. The brief durationof action of this curare-like agent is said to render an antidoteunnecessary if the proper supportive measures are available.Succinylcholine chloride has a disadvantage, however, inthat the usual antidotes cannot terminate its action promptly.

上流・下流製品情報

上流原料

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化合物ノート

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このページの内容基本情報名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
クロロメタン水酸化ナトリウムButanedioic acid, 1,4-bis(2-nitrophenyl) esterButanedioic acid, 1,4-bis(4-nitrophenyl) esterButanedioic acid,1,4-bis(2-chloroethyl) esterこはく酸ビス[2-(ジメチルアミノ)エチル]

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補足説明

定義ChEBI: A chloride salt in which the negative charge of the chloride ions is balanced by succinylcholine dications.