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methoxyflurane

methoxyflurane Structure
CAS No.
76-38-0
Chemical Name:
methoxyflurane
Synonyms
MOZ;MOF;KAT8;hMOF;MYST1;KAT6A;MYST3;ZNF220;DA-759;RUNXBP2
CBNumber:
CB6314297
Molecular Formula:
C3H4Cl2F2O
Molecular Weight:
164.97
MOL File:
76-38-0.mol
MSDS File:
SDS
Modify Date:
2024/3/19 15:37:50

methoxyflurane Properties

Melting point -36°C
Boiling point 103 °C
Density 1.4262
refractive index 1.386
Flash point 37°C
storage temp. -70°C
solubility Chloroform (Sparingly)
form liquid
color Clear
Water Solubility Miscible with alcohol, acetone, chloroform, ether, fixed oils and benzene. Immiscible with water.
Merck 14,5994
BRN 1737766
Exposure limits No exposure limit is set. Based on comparison with related compounds, a TLV-TWA of 675 mg/m3 (100 ppm) is recommended.
Stability Stability
CAS DataBase Reference 76-38-0(CAS DataBase Reference)
EPA Substance Registry System Methoxyflurane (76-38-0)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS07
Signal word  Warning
Hazard statements  H226-H319-H341
Precautionary statements  P210-P241-P308+P311
Hazard Codes  Xi
Risk Statements  10
Safety Statements  23-24/25
RIDADR  3271
OEL Ceiling: 2 ppm (13.5 mg/m3) [60-minute] [*Note: REL for exposure to waste anesthetic gas.]
RTECS  KN7820000
Hazard Note  Irritant
HazardClass  3
PackingGroup  III
HS Code  2909191800
Toxicity 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.
NFPA 704
2
4 0

methoxyflurane price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) SRP5220 KAT8 (2-467), GST tagged human recombinant, expressed in baculovirus infected Sf9 cells, ≥70% (SDS-PAGE), buffered aqueous glycerol solution 2226028-18-6 20μG ₹33388.8 2022-06-14 Buy
ALFA India ALF-L17285-14 2,2-Dichloro-1,1-difluoroethyl methyl ether, 97% 76-38-0 25g ₹18348 2022-05-26 Buy
ALFA India ALF-L17285-06 2,2-Dichloro-1,1-difluoroethyl methyl ether, 97% 76-38-0 5g ₹4605 2022-05-26 Buy
Product number Packaging Price Buy
SRP5220 20μG ₹33388.8 Buy
ALF-L17285-14 25g ₹18348 Buy
ALF-L17285-06 5g ₹4605 Buy

methoxyflurane Chemical Properties,Uses,Production

Chemical Properties

colourless liquid

Uses

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.

Definition

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

Biological Functions

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.

General Description

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.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

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

Health Hazard

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.

Fire Hazard

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

Clinical Use

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.

methoxyflurane Preparation Products And Raw materials

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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 Methoxyfluran Methyl 1,1-difluoro-2,2-dichloroethyl ether Metoxfluran Metoxifluran MOF NSC-110432 Penthrane Pentrane METHOXYFLURANE METOFANE Methoxyflurane (2,2-Dichloro-1,1-difluoroethyl methyl ether) Metofane (2,2-Dichloro-1,1-difluoroethyl methyl ether) 2,2-Dichloro-1,1-difluoroethyl methyl ether 96% 2,2-Dichloro-1,1-difluoro-1-methoxyethane 2-methoxyethane,1,1-dichloro-2,2-difluoro- Analgizer Anecotan DA-759 Ethane, 2,2-dichloro-1,1-difluoro-1-methoxy- Ether, 2,2-dichloro-1,1-difluoroethyl methyl 2,2-Dichloro-1,1-difluoroethylmethylether96% METHOXYFLUORENE 1-Methoxy-1,1-difluoro-2,2-dichloroethane 2,2-Dichloro-1,1-difluoro-1-methoxyethane, 1,1-Dichloro-2,2-difluoro-3-oxabutane FLJ14040 KAT8 (2-467), GST tagged human hMOF Monoclonal Anti-MYST1 antibody produced in mouse