ChemicalBook > CAS DataBase List > Isoflurane

Isoflurane

Product Name
Isoflurane
CAS No.
26675-46-7
Chemical Name
Isoflurane
Synonyms
Forane;Isoflurane266;2-Chloro-2-(difluoromethoxy)-1,1,1-trifluoroethane;1-CHLORO-2,2,2-TRIFLUOROETHYL DIFLUOROMETHYL ETHER;(2R)-2-chloro-2-(difluoroMethoxy)-1,1,1-trifluoroethane;IsofL;Forene;Aerrane;Terrell;Isourane
CBNumber
CB8437691
Molecular Formula
C3H2ClF5O
Formula Weight
184.49
MOL File
26675-46-7.mol
More
Less

Isoflurane Property

Melting point:
48.5°C
Boiling point:
48.5 °C
Density 
1.510 g/mL at 25 °C
vapor pressure 
238 mmHg ( 20 °C)
refractive index 
1.3002
Flash point:
48-49°C
storage temp. 
2-8°C
solubility 
Practically insoluble in water, miscible with ethanol and trichloroethylene.
Specific Gravity
approximate 1.50
color 
Colorless to Almost colorless
Water Solubility 
Soluble in chloroform and ethyl acetate. Not miscible or difficult to mix in water.
Merck 
14,5175
BRN 
1852087
Stability:
Stable.
InChIKey
PIWKPBJCKXDKJR-UHFFFAOYSA-N
CAS DataBase Reference
26675-46-7(CAS DataBase Reference)
NIST Chemistry Reference
1-Chloro-2,2,2-trifluoroethyl difluoromethyl ether(26675-46-7)
EPA Substance Registry System
Isoflurane (26675-46-7)
More
Less

Safety

Hazard Codes 
F,T,Xn
Risk Statements 
36/37/38-67-48/20
Safety Statements 
26-36/37/39-24/25
RIDADR 
UN 3334
WGK Germany 
3
RTECS 
KN6799000
Hazard Note 
Flammable/Toxic
HS Code 
2909191800
Hazardous Substances Data
26675-46-7(Hazardous Substances Data)
Toxicity
An isomer of enflurane with similar anesthetic properties. Isoflurane has less effect on myocardial function, leaving the cardiovascular system normally responsive to epinephrine or hypercarbia, and it does not cause a marked increase in seizure susceptibility. It was not widely used because of reports that it caused increases in liver neoplasms in mice, but this observation has been challenged and the compound reintroduced.
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H336May cause drowsiness or dizziness

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
Y0000858
Product name
Isoflurane
Purity
European Pharmacopoeia (EP) Reference Standard
Packaging
2EA
Price
$161
Updated
2024/03/01
Sigma-Aldrich
Product number
PHR2874
Product name
Isoflurane
Purity
pharmaceutical secondary standard, certified reference material
Packaging
1.2ML
Price
$201
Updated
2024/03/01
Sigma-Aldrich
Product number
792632
Product name
Isoflurane
Packaging
1g
Price
$120
Updated
2024/03/01
Sigma-Aldrich
Product number
1349003
Product name
Isoflurane
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
1ml
Price
$436
Updated
2024/03/01
TCI Chemical
Product number
C2485
Product name
1-Chloro-2,2,2-trifluoroethyl Difluoromethyl Ether
Purity
>98.0%(GC)
Packaging
5g
Price
$50
Updated
2024/03/01
More
Less

Isoflurane Chemical Properties,Usage,Production

Chemical Properties

colourless liquid

Originator

Forane,Ohio Medical,US,1980

Uses

Isoflurane is a volatile anesthetic agent mainly used to study its interaction with the biological system.

Uses

Isoflurane is a halogenated ether used for inhalational anesthesia. Recent studies suggest that there might be a relationship between administration of isoflurane and postoperative cognitive dysfunct ion (POCD).

Uses

Solvent and dispersant for fluorinated materials.

Definition

ChEBI: Isoflurane is an organofluorine compound. It has a role as an inhalation anaesthetic. It is functionally related to a methoxyethane.

Manufacturing Process

A 1-liter 3-necked stainless steel flask was fitted with a copper "Dry Ice" cold finger condenser, a stainless steel stirring shaft and gland and a copper gas inlet tube. To the flask there was then added 50 g (0.23 mol) of CF3CHClOCHCl2 and 1.5 g of SbCl5 · HF gas was then slowly bubbled through the stirred mixture which was maintained at 0°C. The reaction was run until 0.35 mol of HCl was collected, as indicated by the titration of the effluent gas which was dissolved in water. Following the fluorination 26 g of material were recovered and determined to be 90% pure by vapor phase chromatography. Fractional distillation using a 30 x 0.5 cm column packed with glass helices gave the pure product, BP 48°C to 48.5°C.

brand name

Forane (Baxter Healthcare).

Therapeutic Function

Inhalation anesthetic

Biological Functions

Isoflurane (Forane) is a structural isomer of enflurane and produces similar pharmacological properties: some analgesia, some neuromuscular blockade, and depressed respiration. In contrast, however, isoflurane is considered a particularly safe anesthetic in patients with ischemic heart disease, since cardiac output is maintained, the coronary arteries are dilated, and the myocardium does not appear to be sensitized to the effects of catecholamines. Also, blood pressure falls as a result of vasodilation, which preserves tissue blood flow. Isoflurane causes transient and mild tachycardia by direct sympathetic stimulation; this is particularly important in the management of patients with myocardial ischemia.
Unlike enflurane, isoflurane does not produce a seizurelike EEG pattern. Furthermore, the metabolic transformation of isoflurane is only one-tenth that of enflurane, so fluoride production is quite low. Among the halogenated hydrocarbons, isoflurane is one of the most popular, since it preserves cardiovascular stability and causes a low incidence of untoward effects.

General Description

Isoflurane is a volatile liquid (bp=48.5°C) with an MAC of1.15, a blood:gas partition coefficient of 1.43 and high solubilityin fat. Isoflurane is a structural isomer of enflurane. Itis a known respiratory irritant, but less so than desflurane.Approximately 0.2% of the administered drug undergoesmetabolism, the rest is exhaled unchanged. The metabolismof isoflurane yields low levels of the nephrotoxic fluoride ionas well as a potentially hepatotoxic trifluoroacetylating compound). The relatively low concentrations ofthese compounds have resulted in very low risks of hepatotoxicityand nephrotoxicity. There have been no reports ofseizures caused by isoflurane and only transient increases inheart rate have been reported.

Biochem/physiol Actions

Isoflurane is a tandem pore potassium channel activator. It is also a very widely used anesthetic for animal research and for in vitro studies on anesthesia mechanisms.

Clinical Use

Isoflurane was introduced in the United States in 1981 and is a potent anesthetic agent with many similarities to its isomer enflurane (potent, nonflammable, and intermediate blood solubility). It does produce significantly fewer cardiovascular effects than enflurane, however, and it can be used safely with epinephrine without as great a concern for arrhythmia production. Isoflurane has a more pungent odor than halothane and, thus, can cause irritation to the throat and respiratory tract, triggering coughing and laryngospasm. To overcome this problem, it often is supplemented with intravenous agents. Less than 0.2% of an administered dose is metabolized, mostly to fluoride and trifluoroacetic acid. Some minimal potential for hepatotoxicity is associated with a trifluoroacetyl halide metabolite.

Synthesis

Isoflurane is prepared by chlorination of 2,2,2-trifluoroethoxydifluoromethane, itself obtained by alkylation of trifluoroethanol with difluorochloromethane , :

Veterinary Drugs and Treatments

Isoflurane is an inhalant anesthetic that has some distinct advantages over either halothane or methoxyflurane due to its lessened myocardial depressant and catecholamine sensitizing effects, and the ability to use it safely in patients with either hepatic or renal disease. Isoflurane’s higher cost than either methoxyflurane or halothane is a disadvantage.
Horses may recover more rapidly than with halothane, but be more susceptible to anesthetic associated- myopathy.

Isoflurane Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Isoflurane Suppliers

Shandong Yihong Chemical Co. LTD
Tel
13305392349; 15269100373
Fax
0539-7910696
Email
977495915@qq.com
Country
China
ProdList
491
Advantage
58
Jinan Renyuan Chemical Co., Ltd.
Tel
0531-86128689 18396852370
Fax
0531-86128689
Email
1840274076@qq.com
Country
China
ProdList
279
Advantage
58
SHANG FLUORO
Tel
021-65170832 15601903708
Email
qinba_1@163.com
Country
China
ProdList
372
Advantage
60
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TAIYUAN RHF CO.,LTD.
Tel
+86 351 7031519
Fax
+86 351 7031519
Email
sales@RHFChem.com
Country
China
ProdList
2338
Advantage
56
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
ShangHai DEMO Chemical Co.,Ltd
Tel
400-021-7337 2355568890
Fax
0086-21-50182339
Email
sales@demochem.com
Country
China
ProdList
2572
Advantage
57
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44688
Advantage
61
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Fax
86-027-87531808
Email
sales@chemwish.com
Country
China
ProdList
35896
Advantage
56
Shanghai Sinch Parmaceuticals Tech. Co. Ltd.
Tel
+86-21-54098501
Fax
+86-21-54096319
Email
sales@sinch.com.cn
Country
China
ProdList
11598
Advantage
64
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9513
Advantage
66
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Fax
+86-571-82880190
Email
info@yuhaochemical.com
Country
China
ProdList
9387
Advantage
52
Suzhou Sibian Chemical Technology Co.,Ltd.
Tel
0512-65617459 18915409046
Fax
0512-65617459
Email
sales@sibian-chem.com
Country
China
ProdList
1922
Advantage
55
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12335
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22514
Advantage
55
TargetMol Chemicals Inc.
Tel
021-021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7783
Advantage
58
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41462
Advantage
60
ChemStrong Scientific Co.,Ltd
Tel
0755-0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
18070
Advantage
56
Wuhan Dahua Weiye Pharmaceutical Chemical Co., Ltd.
Tel
027-59420981,18702770802
Fax
027-83322098
Country
China
ProdList
1975
Advantage
50
Cool Pharm, Ltd
Tel
021-60455363 18019463053
Fax
50966098
Email
sales@coolpharm.com
Country
China
ProdList
12346
Advantage
58
Chizhou Kailong Import and Export Trade Co., Ltd.
Tel
Fax
-
Email
xg01_gj@163.com
Country
China
ProdList
9484
Advantage
50
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51456
Advantage
80
Quzhou Rundong Chemical (Technology) Co.
Tel
0570-8789886 18892685668
Fax
0570-8789985
Email
info@rundongchemical.com
Country
China
ProdList
3970
Advantage
60
Struchem Co., Ltd.
Tel
0512-0512-63009836 15365350169
Fax
0512-63006936
Email
helen@struchem.com
Country
China
ProdList
3984
Advantage
60
Giant chemicals
Tel
028-85434334 18108076537
Fax
QQ:245797092
Email
market@gianthx.com
Country
China
ProdList
4505
Advantage
56
Shanghai Synchem Pharma Co., ltd
Tel
21-619849051-1 18521059765
Email
synchempharma@aliyun.com
Country
China
ProdList
6463
Advantage
55
Chengdu RunZeBenTu Chemical Co., Ltd
Tel
028-88469284 18000562381
Email
rzbtsj@163.com
Country
China
ProdList
9951
Advantage
56
Henan CoreyChem Co., Ltd
Tel
0371-86658258
Fax
0371-60996044
Email
info@coreychem.com
Country
China
ProdList
10453
Advantage
58
Shanghai QianYan Bio-technology Co., Ltd
Tel
02781293128
Email
orders@biochemsafebuy.com
Country
China
ProdList
9923
Advantage
55
Shandong Xiya Chemical Co., Ltd.
Tel
4009903999 13395398332
Fax
0539-6365991
Email
sales@xiyashiji.com
Country
China
ProdList
20806
Advantage
60
Beijing Solarbio Science & Tecnology Co., Ltd.
Tel
010-50973186 4009686088
Email
3193328036@qq.com
Country
China
ProdList
18338
Advantage
68
Wuhan Magic Biological Technology Co., Ltd.
Tel
18872289958、027-52304252、3400508168
Fax
027-52304252
Email
3400508168@qq.com
Country
China
ProdList
1910
Advantage
55
Guangzhou Jhd Chemical Reagent Co., Ltd.
Tel
020-84383047
Fax
020-84380294
Email
sales@jhd.com.cn
Country
China
ProdList
9186
Advantage
65
Shanghai Orgchem Co.,Ltd.
Tel
+86-21-5877 1921
Fax
+86-21-5877 1925
Email
info@chemofchina.com
Country
China
ProdList
9653
Advantage
55
Lianyungang Xuanyuan Chemical Co., Ltd
Tel
+86-0518-85415818 18000194506
Fax
+86-0518-85415818
Email
18000194506@qq.com
Country
China
ProdList
309
Advantage
55
Shanghai BaiShun Biological Technology Co., Ltd
Tel
021-37581181
Fax
021-57456066
Email
sales@chem-mall.com
Country
China
ProdList
10330
Advantage
58
Capot Chemical Co.,Ltd.
Tel
+86-(0)57185586718 +86-13336195806
Fax
+86-571-85864795
Email
sales@capot.com
Country
China
ProdList
29791
Advantage
60
Aikon International Limited
Tel
025-66028182 18112977050
Fax
(3)02557626880
Email
cfzhang@aikonchem.com
Country
China
ProdList
15818
Advantage
58
Rhawn Reagent
Tel
400-400-1332688 18019345275
Fax
400-133-2688
Email
amy@rhawn.cn
Country
China
ProdList
15497
Advantage
58
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400-638-7771 18920564737
Email
sales@heowns.com
Country
China
ProdList
22872
Advantage
60
3A Chemicals
Tel
400-668-9898
Fax
010-51582189
Email
service@3achem.com
Country
China
ProdList
20557
Advantage
58
Zhengzhou Acme Chemical Co., Ltd.
Tel
0371-037163312495,13303845143 13303845143
Fax
QQ3001379618
Email
3001379618@qq.com
Country
China
ProdList
10386
Advantage
58
Shanghai Jizhi Biochemical Technology Co. Ltd.
Tel
4009004166/18616739031 18616739031
Email
3007523370@qq.com
Country
China
ProdList
52693
Advantage
58
Shanghai Han-Xiang Chemical Co., Ltd.
Tel
15971444841
Fax
18327183813
Email
amber@biochempartner.com
Country
China
ProdList
3061
Advantage
58
Shanghai Hongye Biotechnology Co. Ltd
Tel
400-9205774
Email
sales@glpbio.cn
Country
China
ProdList
6777
Advantage
58
ANHUI WITOP BIOTECH CO., LTD
Tel
+8615255079626
Email
eric@witopchemical.com
Country
China
ProdList
23541
Advantage
58
More
Less

View Lastest Price from Isoflurane manufacturers

Wuhan Boyuan Import & Export Co., LTD
Product
Isoflurane 26675-46-7
Price
US $20.00-10.00/kg
Min. Order
1kg
Purity
99.60%
Supply Ability
50tons
Release date
2023-12-11
Hebei Ningnan Trade Co. LTD
Product
Isoflurane 26675-46-7
Price
US $10.00/G
Min. Order
1G
Purity
99.99%
Supply Ability
20MT
Release date
2022-10-24
Jinan Shengqi pharmaceutical Co,Ltd
Product
Isoflurane 26675-46-7
Price
US $0.00/KG
Min. Order
1KG
Purity
99
Supply Ability
10MT
Release date
2019-03-21

26675-46-7, IsofluraneRelated Search:


  • Isoflurane266
  • ether,1-chloro-2,2,2-trifluoroethyldifluoromethyl
  • Forane
  • Forene
  • r-e235dal
  • 1-Chloro-2,2,2-trifluoroethyl difluoromethyl ether 99%
  • 1-Chloro-2,2,2-trifluoroethyldifluoromethylether99%
  • 2-chloro-2-(difluoromethoxy)-1,1,1-trifluoro-ethan
  • 2-Chloro-2-(difluoromethoxy)-1,1,1-trifluoroethane
  • Aerrane
  • chloro-2-(difluoromethoxy)-1,1,1-trifluoroethane
  • chloro-2,2,2-trifluorodifluoromethylether
  • Compd 469
  • Compound 469
  • Ethane, 1-chloro-1-(difluoromethoxy)-2,2,2-trifluoro-
  • Ethane, 2-chloro-2-(difluoromethoxy)-1,1,1-trifluoro-
  • Ether, 1-chloro-2,2,2-trifluoroethyl difluoromethyl
  • Difluoromethyl 1-chloro-2,2,2-trifluoroethyl ether (Isoflurane)
  • Isourane
  • IsofL
  • Difluoromethyl 1-chloro-2,2,2-trifluoroethyl ether
  • Ethane, 2-chloro-2-(difluoromethoxy)-1,1,1-trifluoro- (9CI)
  • HCFE 235da2
  • R-E 235da1
  • ISOFLUORENE
  • 1-CHLORO-2,2,2-trifiuoroethyl dinuoromethyl ether
  • Isourane (1 mL)
  • Isoflurane (1 mL)
  • (2R)-2-chloro-2-(difluoroMethoxy)-1,1,1-trifluoroethane
  • 2-Chloro-2-(difluoromethoxy)-1,1,1-trifluoroethane Isoflurane
  • 1-CHLORO-2,2,2-TRIFLUOROETHYL DIFLUOROMETHYL ETHER
  • ISOFLURANE
  • 1-Chloro-2,2,2-trifluoroethyl ether
  • 1-Chloro-2,2,2-trifluoroethyldrfluoromethylether
  • Isoflurane CRS
  • Isoflurane RS
  • lsoflurane
  • HSDB 8057
  • HSDB8057
  • HSDB-8057
  • Terrell
  • Isoflurane (1349003)
  • 1-Chloro-2,2,2-trifluoroethyl difluoromethyl ether, 98+%
  • 26675-46-7
  • C3H2CIF5O
  • CF3CHClOCHF2