メトキシフルラン

メトキシフルラン 化学構造式
76-38-0
CAS番号.
76-38-0
化学名:
メトキシフルラン
别名:
メトキシフルラン;メトキシフルレン;1,1-ジフルオロ-2,2-ジクロロエチルメチルエーテル;2,2-ジクロロ-1,1-ジフルオロ-1-メトキシエタン;メチル1,1-ジフルオロ-2,2-ジクロロエチルエーテル;メトファン;(2,2-ジクロロ-1,1-ジフルオロエチル)メチルエーテル;ペントラン;ペントレン
英語名:
methoxyflurane
英語别名:
MOZ;MOF;KAT8;hMOF;MYST1;KAT6A;MYST3;ZNF220;DA-759;RUNXBP2
CBNumber:
CB6314297
化学式:
C3H4Cl2F2O
分子量:
164.97
MOL File:
76-38-0.mol

メトキシフルラン 物理性質

融点 :
-36°C
沸点 :
103 °C
比重(密度) :
1.4262
屈折率 :
1.386
闪点 :
37°C
貯蔵温度 :
-70°C
溶解性:
Chloroform (Sparingly)
外見 :
liquid
色:
Clear
水溶解度 :
アルコール、アセトン、クロロホルム、エーテル、固定油、ベンゼンと混和します。水と混和しない。
Merck :
14,5994
BRN :
1737766
暴露限界値:
No exposure limit is set. Based on comparison with related compounds, a TLV-TWA of 675 mg/m3 (100 ppm) is recommended.
安定性::
安定
CAS データベース:
76-38-0(CAS DataBase Reference)
EPAの化学物質情報:
Methoxyflurane (76-38-0)
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
主な危険性  Xi
Rフレーズ  10
Sフレーズ  23-24/25
RIDADR  3271
OEL Ceiling: 2 ppm (13.5 mg/m3) [60-minute] [*Note: REL for exposure to waste anesthetic gas.]
RTECS 番号 KN7820000
Hazard Note  Irritant
国連危険物分類  3
容器等級  III
HSコード  2909191800
有毒物質データの 76-38-0(Hazardous Substances Data)
毒性 One of the most potent of the inhalational anesthetics, having a very high blood-gas partition coefficient and low vapor pressure at room temperature. Methoxyflurane is metabolized to a great extent (about 50-70%) in the liver and, as a consequence, there may be release of high concentrations of fluoride, sufficient to exceed the threshold for renal damage. Its use for sustained anesthesia is limited because of this renal toxicity and was discontinued around 1980.
絵表示(GHS) GHS hazard pictogramsGHS hazard pictograms
注意喚起語
危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H226 引火性の液体および蒸気 引火性液体 3 警告
H319 強い眼刺激 眼に対する重篤な損傷性/眼刺激 性 2A 警告 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H341 遺伝性疾患のおそれの疑い 生殖細胞変異原性 2 警告 P201,P202, P281, P308+P313, P405,P501
注意書き
P210 熱/火花/裸火/高温のもののような着火源から遠ざ けること。-禁煙。
P241 防爆型の電気機器/換気装置/照明機器/...機器を使 用すること。

メトキシフルラン 価格 もっと(6)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01TRCM262675 メトキシフルラン
Methoxyflurane
76-38-0 1g ¥65100 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01TRCM262675 メトキシフルラン
Methoxyflurane
76-38-0 10g ¥514200 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) SAB4503328 Anti-MYST1 antibody produced in rabbit affinity isolated antibody
affinity isolated antibody
76-38-0 100μg ¥97700 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) SAB1411501 Anti-MYST1 antibody produced in rabbit purified immunoglobulin, buffered aqueous solution
purified immunoglobulin, buffered aqueous solution
76-38-0 100μg ¥78600 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) SAB1306205 ANTI-HMOF/MYST1(C-TERMINAL) antibody produced in rabbit purified immunoglobulin, buffered aqueous solution
purified immunoglobulin, buffered aqueous solution
76-38-0 400μL ¥89100 2024-03-01 購入

メトキシフルラン 化学特性,用途語,生産方法

効能

吸入麻酔薬

化学的特性

colourless liquid

使用

Methoxyflurane is a very potent and highly lipid soluble anesthetic agent. Methoxyflurane causes deep sedation and it has been used as a patient controlled analgesic for painful procedures in children. Methoxyflurane is a significant respiratory depressant.

定義

ChEBI: An ether in which the two groups attached to the central oxygen atom are methyl and 2,2-dichloro-1,1-difluoroethyl.

生物学の機能

Methoxyflurane (Penthrane) is the most potent inhalational agent available, but its high solubility in tissues limits its use as an induction anesthetic. Its pharmacological properties are similar to those of halothane with some notable exceptions. For example, since methoxyflurane does not depress cardiovascular reflexes, its direct myocardial depressant effect is partially offset by reflex tachycardia, so arterial blood pressure is better maintained. Also, the oxidative metabolism of methoxyflurane results in the production of oxalic acid and fluoride concentrations that approach the threshold of causing renal tubular dysfunction. Concern for nephrotoxicity has greatly restricted the use of methoxyflurane.

一般的な説明

Methoxyflurane is a volatile liquid (bp=105°C) with a highblood:gas partition coefficient and thus a slow induction andprolonged recovery. Approximately 75% of the drug undergoesmetabolism yielding dichloroacetate, difluoromethoxyacetate,oxalate, and fluoride ions. The intrarenal inorganicfluoride concentration, as a result of renal defluorination, maybe responsible for the nephrotoxicity seen with methoxyflurane.Both the concentration of F- generated and the durationfor which it remained elevated were factors in the developmentof methoxyflurane nephrotoxicity. Methoxyfluranewas removed from the U.S. market in 2000 because of saferalternatives. Both isoflurane and enflurane produce less fluorideion upon metabolism than methoxyflurane.

空気と水の反応

Insoluble in water.

反応プロフィール

2,2-DICHLORO-1,1-DIFLUOROETHYL METHYL ETHER may be sensitive to prolonged exposure to light.

健康ハザード

Methoxyflurane exhibited low to very lowacute toxicity via inhalation, slightly lowerthan that of ethrane. Oral toxicity was low tomoderate depending on the species. Inhala tion of its vapors at 1.5–2% by volumeconcentrations in air can cause anesthesia inhumans. The toxic symptoms are similar tothose of ethrane, and the target organs areprimarily the central nervous system, kidney,and liver. At subanesthetic concentrations of0.3–0.5% by volume in air, its exposure tohumans for 1 hour resulted in the onset oflow toxicity. The sites of biological effectswere in the kidney.
LC50 value, inhalation (mice): 17,500 ppm/2 hr
LD50 value, oral (mammals): 3600 mg/kg
The liquid may be an irritant to theeyes. The teratomeric properties of this com pound were observed in rats and mice. Thesymptoms were embryo deaths and develop mental abnormalities in the urogenital andmusculoskeletal systems.
No carcinogenic actions in animals orhumans have been reported. The histidinereversion–Ames test for mutagenicity wasinconclusive.

火災危険

2,2-DICHLORO-1,1-DIFLUOROETHYL METHYL ETHER is combustible.

臨床応用

Methoxyflurane is seldom used because of its propensity to cause renal toxicity. It is the most potent agent, and it has the highest solubility in blood. Induction and recovery would be expected to be slow. Chemically, it is rather unstable, and as much as 50% of an administered dose can be metabolized. Toxic metabolites significantly limit its utility as a general anesthetic.

メトキシフルラン 上流と下流の製品情報

原材料

準備製品


メトキシフルラン 生産企業

Global( 89)Suppliers
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SHANGHAI KEAN TECHNOLOGY CO., LTD.
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76-38-0(メトキシフルラン)キーワード:


  • 76-38-0
  • RUNXBP2
  • ZNF220
  • Anti-MYST1 antibody produced in rabbit
  • MOZ
  • MYST protein 1
  • SAS2 and TIP60 protein 1
  • YBF2/SAS3
  • ANTI-HMOF/MYST1(C-TERMINAL) antibody produced in rabbit
  • Histone acetyltransferase KAT8
  • KAT8
  • Lysine acetyltransferase 8
  • MYST1
  • 1,1-dichloro-2,2-difluoro-2-methoxyethane
  • 2,2-dichloro-1,1-difluoro-1-methoxy-ethan
  • Methoxyflurane, 2,2-Dichloro-1,1-difluoro-1-methoxyethane
  • Methoxyflurane (1 mL)
  • 2,2-DICHLORO-1,1-DIFLUOROETHYL METHYL ETHER
  • 1,1-difluoro-2,2-dichloroethyl methyl ether
  • Methflurane
  • Methoxflurane
  • METHOXYFLURANE (METOFANE)
  • ether,2,2-dichloro-1,1-difluoroethylmethyl
  • Ingalan
  • Inhalan
  • Methofane
  • Methoflurane
  • Methoxane
  • Methoxiflurane
  • Methoxyfluoran
  • Methoxyfluorane
  • メトキシフルラン
  • メトキシフルレン
  • 1,1-ジフルオロ-2,2-ジクロロエチルメチルエーテル
  • 2,2-ジクロロ-1,1-ジフルオロ-1-メトキシエタン
  • メチル1,1-ジフルオロ-2,2-ジクロロエチルエーテル
  • メトファン
  • (2,2-ジクロロ-1,1-ジフルオロエチル)メチルエーテル
  • ペントラン
  • ペントレン
  • 麻酔薬
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