StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Verbindung

Diisopropylether

Diisopropyl Ether

HCID 7914
Neue NotizNeue ReaktionAnfrage stellen
Druckvorschau

Daten werden ergänzt – lade die Seite später neu, um den aktuellen Stand zu sehen

GrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
TeilstruktursucheÄhnliche Strukturen suchen

Grundinformationen

CAS
108-20-3
Standard-SMILES
CC(C)OC(C)C
InChIKey
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N
Summenformel
C6H14O
Durchschnittliche Molmasse
102,17 g/mol
Monoisotopische Masse
102,10446507

Überblick

Diisopropyl ether appears as a clear colorless liquid with an ethereal odor. Flash point -18 °F. Less dense than water. Vapors heavier than air.

Namen und Bezeichner

Bevorzugter Name
Diisopropyl Ether
IUPAC
2-propan-2-yloxypropane
Lokaler Name
Diisopropylether
Englischer Name
Diisopropyl ether
Summenformel
C6H14O
Molmasse
102.17

Namen und Synonyme

Diisopropyl etherISOPROPYL ETHER108-20-32-IsopropoxypropanePropane, 2,2'-oxybis-Diisopropyl oxideEther, isopropylBis(isopropyl) etherIzopropylowy eterEther isopropylique2,2'-OxybispropaneDTXSID4021890
Weitere Namen anzeigen
DIPEDiisopropyl etheIsoprpyl etherDiisoproyl etherISOPROPYL ETHER, 1000MG, NEAT
DO7Y998826DTXCID4018902-Isopropoxy propaneRefChem:134066203-560-6diisopropylether2,2'-oxydipropane2-propan-2-yloxypropane

Datenbank-Bezeichner

CAS
108-20-3
PubChem CID
7914
DTXSID
DTXSID4021890
ChEMBL
CHEMBL3185565
UNII
DO7Y998826
EC Number
203-560-6
Nikkaji
J5.069E

Eigenschaften

Berechnete StruktureigenschaftenWird ergänzt

XLogP
1,5
Polarare Oberfläche (TPSA)
9,2 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
1
Frei drehbare Bindungen
2
Schwere Atome
7
Formalladung
0
Komplexität
33,4

Experimentelle und physikochemische Eigenschaften

Chemical Classes · 2 Einträge

Flammable agents - 3rd degree

Volatile Organic Compound (VOC)

SolventsSolvents -> Ethers (<C12)
SpringerMaterials PropertiesSchoenflies notation
LogP · 2 Einträge

log Kow= 1.52

1.94

Odor · 4 Einträge

Sweet, slightly sharp, pungent like camphor and ethyl ether

The odor is more irritating and less pleasant than that of ethyl ether.

Sharp, sweet, ether-like odor.

Ether-like odor

Density · 6 Einträge

0.724 at 68 °F (USCG, 1999) - Less dense than water; will float

0.7258 @ 20 °C/4 °C

Bulk density: 6.05 lb/gal @ 15.5 °C; similar to ethyl ether in properties but does tend to form peroxides more readily than ethyl ether

Relative density (water = 1): 0.7

0.73

0.719 @25 °C

Viscosity0.273 centipoise at 20 °F

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H225: Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P271, P280, P303+P361+P353, P304+P340, P319, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

This chemical does not meet GHS hazard criteria for 0.4% (1 of 265) of reports.

Danger

H225 (99.6%): Highly Flammable liquid and vapor [Danger Flammable liquids]

Gefahrenhinweise

Regulatory Information · 5 Einträge

Chemical: Propane, 2,2'-oxybis-

Propane, 2,2'-oxybis- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Propane, 2,2'-oxybis- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 13-01-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/15860

Propane, 2,2'-oxybis-: HSNO Approval: HSR001131 Approved with controls

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

DOT LabelFlammable Liquid
Fire Hazards · 3 Einträge

Behavior in Fire: Vapor is heavier than air and may travel a considerable distance to a source of ignition and flash back. Containers may explode when heated. (USCG, 1999)

· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.

Highly flammable. Vapour/air mixtures are explosive.

Fire Potential · 2 Einträge

FLAMMABLE LIQUID.

ONLY ELECTRICAL EQUIPMENT OF EXPLOSION-PROOF TYPE (GROUP C CLASSIFICATION) IS PERMITTED TO BE OPERATED IN ETHER AREAS. ETHER SHOULD NOT BE STORED NEAR POWERFUL OXIDIZERS OR IN AREAS OF HIGH FIRE HAZARD. /ETHERS/

Chemie und Industrie

Pharmakologische Informationen

Absorption, Distribution and Excretion... ISOPROPYL ETHER IS RAPIDLY ABSORBED BY BLOOD FROM LUNGS OR GI TRACT. ... IT IS PROBABLE THAT MAJOR PORTION OF DOSE IS ELIMINATED THROUGH LUNGS AFTER CESSATION OF EXPOSURE ... .

Verwendung und Herstellung

Uses · 6 Einträge

Used as a solvent for resins, waxes, oils, dyes, and surface coatings; [ACGIH]

Painting (Solvents) [Category: Paint]

Solvent for animal, vegetable, mineral oils, waxes and resins; extraction of acetic acid from aq solutions; solvent for dyes in presence of small amt of alcohol; spotting compositions; paint & varnish; rubber cements.

Isopropyl ether is used as a solvent in the Israel Mining Industries acid cleaning process for extraction of cationic impurities. /anionic impurities to a much lesser extent/

Isopropyl ether is used as a solvent to separate polonium from lead and bismuth.

Extraction agent (phosphoric acid, phenol purification); solvent (paints, stain removers)

Impurities · 3 Einträge

COMMERCIAL VARIETY MAY CONTAIN APPROX 3% OF ISOPROPYL ALC, LESS THAN 0.01% OF SULFUR & LESS THAN 0.04% OF PEROXIDE.

The dehydration of isopropyl alcohol with sulfuric acid produces propylene as an impurity in the production of isopropyl ether. The amounts of propylene by-product will vary with type of catalyst and reaction conditions.

Isopropyl ether autooxidizes to form peroxides and hydroperoxides at 20 °C with UV radiation or in the presence of a photosensitizer, eg, benzophenone

U.S. Imports(1984) 2.49X10+8 g
U.S. Production · 2 Einträge

2023: 40,000,000 - <55,000,000 lb

(1972) PROBABLY GREATER THAN 4.54X10+5 G

Consumer UsesFuel agents
Industry UsesFuel agents

Zugehörige Reaktionen

2.836
Reaktionsaufzeichnung erstellen
Reaktionsgleichung von HRID 1024
HRID 1024als Eduktuspto-grants-1998_03
Reaktionsgleichung von HRID 1081
HRID 1081als Eduktuspto-grants-1998_03
Reaktionsgleichung von HRID 2923
HRID 2923als Lösungsmitteluspto-grants-1998_03
Reaktionsgleichung von HRID 4594
HRID 4594als Eduktuspto-grants-1988_02
Reaktionsgleichung von HRID 4595
HRID 4595als Eduktuspto-grants-1988_02
Reaktionsgleichung von HRID 5089
HRID 5089als Lösungsmitteluspto-grants-1993_09
Reaktionsgleichung von HRID 5514
HRID 5514als Lösungsmitteluspto-grants-1993_09
Reaktionsgleichung von HRID 5520
HRID 5520als Eduktuspto-grants-1993_09
Seite 1 von 355

Notizen zur Verbindung

Wird geladen…

Auf dieser SeiteGrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
Weitere Aktionen
Neue NotizNeue ReaktionAnfrage stellen
Color/Form · 3 Einträge

Colorless volatile liquid

Colorless liquid.

Colorless liquid

Solubility · 6 Einträge

0.2 % (NIOSH, 2024)

Sol of commercial grade in water, 1.71% @ 19 °C; miscible with most organic solvents.

Sol in acetone; miscible in ethyl alcohol, ethyl ether

MISCIBLE WITH MOST ORG SOLVENTS

Water solubility = 8,800 mg/l @ 20 °C

Soluble in oxygenated solvents

Flash Point · 6 Einträge

-18 °F (USCG, 1999)

-28 °C

-18 °F (-28 °C) (closed cup)

-28 °C

-18 °F

-18 °F

Boiling Point · 6 Einträge

156 °F at 760 mmHg (USCG, 1999)

68.5 °C

69 °C

154 °F

68.5 °C @760 [mm Hg]

154 °F

DecompositionWhen heated to decomposition it emits acrid smoke and fumes.

Physikochemische Eigenschaften

Schmelzpunkt
-85.5 °C · -85.5 °C
Siedepunkt
68 · 68-69 °C(lit.)
Dichte
0.725 g/mL · 0.725 g/mL at 25 °C(lit.)
Dampfdichte
3.5 · 3.5 (vs air)
Dampfdruck
120 mm · 120 mm Hg ( 20 °C)
Brechungsindex
20 · n20/D 1.367(lit.)
Flammpunkt
29 °F · −29 °F
storage temp.
30 °C · Store below +30°C.
Löslichkeit
3.11 g/l · 3.11g/l
Aggregatzustand
Liquid
Farbe
25 · APHA: ≤25
Geruch (Odor)
Sweet, slightly sharp; characteristic pungent; ethereal; like amphor and ethyl ether.
PH
7 · 7 (20°C)
Explosionsgrenze
1 · 1-21%, 100°F
Wasserlöslichkeit
9 g/L · 9 g/L (20 ºC)
Spezifische Wärmekapazität
2.12 J/ · Cp(liquid): 2.12 J/(g·K), at 25℃
Merck
14 · 14,5212
BRN
1731256 · 1731256
Henry's Law Constant
2.57 at · 2.57 at 25 °C (headspace-GC, Arp and Schmidt, 2004)
Dielectric constant
3.9 · 3.9(25℃)
Stabilität
Extremely flammable. This material is a serious fire and explosion risk. Vapour may travel considerable distances to an ignition source, which need not be an open flame, but may be a hot plate, steam pipe, etc. Vapour may be ignited by the static electricty which can build up when isopropyl ether is being poured from one vessel
InChI
1S/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3
InChIKey
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N
SMILES
CC(C)OC(C)C
LogP
2.4 at · 2.4 at 20℃
Oberflächenspannung
17.74 mN/m · 17.74mN/m at 293.15K
CAS Datenbank
108 · 108-20-3(CAS DataBase Reference)
NIST chemische Informationen
Diisopropyl ether(108-20-3)
EPA chemische Informationen
Isopropyl ether (108-20-3)
Health Hazards · 2 Einträge

Inhalation causes anesthesia, nausea, headache, dizziness, and irritation of the eyes and nose. Contact of liquid with eyes causes only minor injury; repeated contact with skin will remove natural oils and may cause dermatitis. (USCG, 1999)

· Inhalation or contact with material may irritate or burn skin and eyes.

Hazards SummaryThe odor is more irritating and less pleasant than that of ethyl ether. [ACGIH] A skin, eye, and respiratory tract irritant; Inhalation of high concentrations can cause CNS depression; [ICSC]
DOT ID and Guide · 2 Einträge

1159 127

1159 127

Reactive GroupEthers
EC ClassificationSymbol: F; R: 11-19-66-67; S: (2)-9-16-29-33; Note: C
UN ClassificationUN Hazard Class: 3; UN Pack Group: II
Reactivity AlertsHighly Flammable
OSHA StandardsPermissible Exposure Limit: Table Z-1 8-hr Time Weighted Avg: 500 ppm (2100 mg/cu m).

Sicherheit und Schutzausrüstung

Fire Fighting · 2 Einträge

Excerpt from ERG Guide 127 [Flammable Liquids (Water-Miscible)]:

Use water spray, AFFF, powder, alcohol-resistant foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.

First Aid Measures · 4 Einträge

Fresh air, rest. Refer for medical attention.

Remove contaminated clothes. Rinse skin with plenty of water or shower.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Rest. Refer for medical attention .

Accidental Release Measures · 2 Einträge

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

First Aid · 3 Einträge

Excerpt from NIOSH Pocket Guide for Isopropyl ether:

General First Aid:

(General first aid procedures)

Safe StorageFireproof. Cool. Keep in the dark. Keep in a well-ventilated room. Store only if stabilized.
Firefighting HazardsVAPORS ARE HEAVIER THAN AIR & MAY TRAVEL TO A SOURCE OF IGNITION & FLASH BACK. LIQUID FLOATS ON WATER & MAY TRAVEL TO A SOURCE OF IGNITION & SPREAD FIRE. ETHER TENDS TO FORM UNSTABLE, EXPLOSIVE PEROXIDES ON STANDING.
Exposure Control and Personal Protection · 2 Einträge

· Wear positive pressure self-contained breathing apparatus (SCBA).

200.0 [ppm]

Fire Fighting ProceduresAlcohol foam, CO2, foam, dry chemical.
Storage ConditionsStore in cool, dry, well-ventilated location. Separate from acids & oxidizing materials.
Cleanup Methods · 1 Eintrag

1. Remove all ignition sources. 2. Ventilate area of spill or leak. 3. For small quantities, absorb on paper towels. Evaporate in a safe place (such as fume hood). Allow sufficient time for evaporating vapors to completely clear the hood ductwork. Burn the paper in a suitable location away from combustible materials. Large quantities can be reclaimed or collected and atomized in a suitable combustion chamber.

Nonfire Spill ResponseExcerpt from ERG Guide 127 [Flammable Liquids (Water-Miscible)]:
Disposal Methods · 5 Einträge

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Isopropylether may be disposed of by atomizing in a suitable combustion chamber.

Isopropyl ether is a waste chemical stream constituent which may be subjected to ultimate disposal by controlled incineration.

The following wastewater treatment technologies have been investigated for isopropyl ether: Concentration process: Biological treatment.

For more Disposal Methods (Complete) data for ISOPROPYL ETHER (8 total), please visit the HSDB record page.

Toxikologische Informationen

Target OrgansEyes, skin, respiratory system, central nervous system
Ecotoxicity ValuesLC50 Pimephales promelas (fathead minnow) 91.7 mg/l 96 hr flow-through bioassay, wt 0.12 g, water hardness 45.5 mg/l CaCO3, temp: 25 + or - 1 °C, pH 7.5, dissolved oxygen greater than 60% of saturation
Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 160(SRC), determined from a log Kow of 1.52(2) and a regression-derived equation(3), indicates that isopropyl ether is expected to have high mobility in soil(SRC). Volatilization of isopropyl ether from moist soil surfaces is expected to be important(3,SRC) given an estimated Henry's Law constant of 2.3X10-3 atm-cu m/mole(SRC), calculated from its water solubility(4) and vapor pressure(5). The potential for volatilization of isopropyl ether from dry soil surfaces may exist(SRC) based on a vapor pressure of 149 mm Hg(5). Isopropyl ether is not expected to hydrolyze in soil due to lack of hydrolyzable functional groups(3). Aqueous screening test data from studies using activated sludge or sewage inocula(6,7) suggest that isopropyl ether may be resistant to biodegradation in environmental media(SRC). Many ethers are known to be resistant to biodegradation(8).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 160(SRC), determined from a log Kow of 1.52(2) and a regression-derived equation(3), indicates that isopropyl ether is not expected to adsorb to suspended solids and sediment in water(SRC). Isopropyl ether is expected to volatilize rapidly from water surfaces(3,SRC) based on an estimated Henry's Law constant of 2.3X10-3 atm-cu m/mole(SRC), calculated from its water solubility(4) and vapor pressure(5). Estimated volatilization half-lives for a model river and model lake are 3 hours and 4 days, respectively(3,SRC). Isopropyl ether is not expected to undergo hydrolysis in the environment due to the lack of hydrolyzable functional groups(3). Isopropyl ether will not significantly photooxidize via reaction with photochemically produced hydroxyl radicals in the water(6). According to a classification scheme(7), an estimated BCF of 8(3,SRC), from isopropyl ether's log Kow(2), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Isopropyl ether may be resistant to biodegradation in environmental media based upon screening test data from studies using activated sludge or sewage inocula(8,9,SRC). Many ethers are known to be resistant to biodegradation(10).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), isopropyl ether, which has a vapor pressure of 149 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase isopropyl ether is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 21 hours(3,SRC). The half-life for the reaction of isopropyl ether with nitrate radicals is estimated as 9 seconds(4,SRC). Direct photolysis will not be an important removal process since aliphatic ethers do not absorb light at wavelengths >290 nm(5).

Adverse EffectsNeurotoxin - Acute solvent syndrome
Exposure Routes · 2 Einträge

The substance can be absorbed into the body by inhalation of its vapour.

inhalation, ingestion, skin and/or eye contact

Signs and Symptoms · 5 Einträge

Cough. Drowsiness. Sore throat.

Dry skin. Redness.

Redness.

Further see Inhalation.

irritation eyes, skin, nose; resp discomfort; dermatitis; In Animals: drowsiness, dizziness, unconsciousness, narcosis

Effluent Concentrations · 1 Eintrag

Isopropyl ether has been detected in 10 out of 63 samples of industrial effluents collected from a wide variety of industries across the USA (dates not reported)(1). Six of the positive samples contained <10 ug/L isopropyl ether, 3 samples contained 10-100 ug/L and 1 sample contained >100 ug/L(1). Samples of landfill gas from an unspecified landfill which had for more than 15 months accepted municipal and industrial solid wastes and unspecified liquid wastes contained 220 mg/cu m isopropyl ether(2).

Medical Surveillance · 1 Eintrag

Employees should be screened for history of certain medical conditions /chronic respiratory disease or skin disease/ which might place the employee at increased risk from isopropylether exposure. In persons with impaired pulmonary function, especially those with obstructive airway diseases, the breathing of isopropylether might cause exacerbation of symptoms due to its irritant properties. Isopropylether is a defatting agent and can cause dermatitis on prolonged exposure. Persons with existing skin disorders may be more susceptible to the effects of this agent. Any employee developing the above-listed conditions should be referred for further medical examination. /Chronic respiratory disease or skin disease/

Soil Adsorption/Mobility · 1 Eintrag

The Koc of isopropyl ether is estimated as approximately 160(SRC), using a log Kow of 1.52(1) and a regression-derived equation(2,SRC). According to a classification scheme(3), this estimated Koc value suggests that isopropyl ether is expected to have high mobility in soil(SRC).

Atmospheric ConcentrationsIsopropyl ether was identified, but not quantified, at 4 of 7 sites in the Kanawha Valley, WV, sampled in Sept 1977(1).
Human Toxicity Excerpts · 5 Einträge

Toxic symptoms similar to ethyl ether.

MILDLY IRRITATING TO SKIN, MUCOUS MEMBRANES. INHALATION OF HIGH CONCENTRATIONS CAUSES /CNS DEPRESSION/, UNCONSCIOUSNESS. DEATH MAY OCCUR DUE TO RESP PARALYSIS. /ETHYL ETHER/

Isopropyl ether has an anesthetic action very much like ethyl ether, but is somewhat more toxic.

Human exposure to 500 ppm over a 15 min period caused no irritation, but irritation of the eyes and nose was noted at 800 ppm for 5 min with some respiratory discomfort. Industrial exposure has caused but few cases of death or serious injury. Repeated skin contact would be expected to cause dermatitis.

... a group of subjects exposed for 15 minutes at 500 ppm did not consider the exposure to be irritating. At a concentration of 300 ppm, however, about one-third of the subjects objected to the unpleasant odor, while at 800 ppm for five minutes most subjects reported irritation of the eyes and nose.

Artificial Pollution SourcesIsopropyl ether's production and use as an extraction agent and as a solvent in paints/stain removers(1) may result in its release to the environment through various waste streams(SRC).

Regulatorische Informationen

State Drinking Water Guidelines(NH) NEW HAMPSHIRE 120 ug/L

Sicherheitsdaten

F
10
OEB
A
OEL
TWA: 500 ppm (2100 mg/m3)
wgk
1
IDLA
1,400 ppm [10% LEL]
tsca
TSCA listed
ridadr
UN 1159
hs_code
2909 19 90
RTECS-Nr.
TZ5425000
risk_code
11-19-66-67-52/53
Toxizität
LD50 in 14 day old, young adult, adult rats (ml/kg): 6.4, 16.5, 16.0 orally (Kimura)
hazard_code
F
safety_code
9-16-29-33-61
hazard_class
3
packing_group
II
Speicherklasse
3 - Flammable liquids
Giftige Stoffe Daten
108-20-3(Hazardous Substances Data)
Hazard Classifications
Flam. Liq. 2STOT SE 3
Selbstentzündungstemperatur
827 °F
Methods of Manufacturing · 2 Einträge

PREPARED ... AS BY-PRODUCT OF PRODN OF ISOPROPYL ALC FROM CRACKED GASOLINE.

Obtained in large quantities as a by-product from the manufacture of isopropyl alcohol from propylene by the sulfuric acid process.

Formulations/Preparations · 3 Einträge

Grade: technical.

Purity: 94+%. May contain 0.01% hydroquinone or other inhibitor to prevent peroxide formation

USUALLY CONTAINS P-BENZYLAMINOPHENOL AS STABILIZER.

Use ClassificationFood Additives -> EXTRACTION_SOLVENT -> JECFA Functional Classes
General Manufacturing Information · 2 Einträge

Pharmaceutical and Medicine Manufacturing

Propane, 2,2'-oxybis-: ACTIVE

Anwendungen · 2 Einträge

BeschreibungDiisopropyl ether [108-20-3], also known as 2-isopropoxyisopropane or isopropyl ether, is a clear, colorless, mobile, highly flammable liquid with a characteristic ethereal odor. Its solubility in water is low, but it is soluble in organic solvents and readily forms explosive peroxides. It has a higher boiling point, a lower vapor pressure, and a lower water solubility than diethyl ether, which means that diisopropyl ether can be recovered without significant loss after use as a solvent or as an extractant.

VerwendenIsopropyl ether is used as a solvent for oils,waxes, resins, and dyes; and as a varnishremover.

Darstellung

synthetischeDiisopropyl ether can be prepared by liquid-phase dehydration of 2-propanol at 130 – 190°C and 1.96– 7.85 MPa over acidic catalysts containing aluminum.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

SchwefelwasserstoffSchwefelsäure-bis(1-methylethyl)-esterPropan-2-ol

Nachgelagerte Produkte

((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-benzopyran-6-ylacetat2,3-Dimethyl-pyridin-4-ylamineN-ethyl perfluorooctylsulfonylaminoacetateZopiclonAcemetacinPhenyl(piperidin-4-yl)methanoneS,S-Dimethylcyanimidodithio-carbonatEthyl 3-bromo-2-(bromomethyl)propionate1-Acetyl-4-benzoylpiperidineN-ACRYLOXYSUCCINIMIDE4-Amino-3-nitroquinolineNizofenoneDisoprofol6-Amino-1H-pyrimidin-4-onEthyl 5-nitroindole-2-carboxylate4-Hydrazino-6-hydroxypyrimidineEflornithine2-(Piperazin-1-yl)-acetic acid N-(2-phenylethyl)-amide1-(2-Pyridin-2-yl-ethyl)-piperazineManidipineCyclen(4-Amino-3-nitrophenyl)-(2-thienyl)methanoneCHILLIORANGEMifepristone3-Butoxyphenol4-Chloro-3-nitroquinoline3-(3,5-Dichlorphenyl)-2,4-dioxo-N-isopropylimidazolidin-1-carboxamid3,4-Dichloro-N-methylaniline1-Boc-4-(4-formylphenyl)piperazine1R,3R-chrysanthemic acidCeftazidimEthyl 5-amino-1H-indole-2-carboxylateTiclopidine1-Acetylpiperidin-4-carbonsure(4-Methoxy-3-nitrophenyl)-(thiophen-2-yl)methanone ,98%Methyl 8-aminoquinoline-4-carboxylate3-Bromo-2-(bromomethyl)propionic acid6-Chloropyrimidin-4(3H)-oneN-(2-Chlorethyl)pyrrolidinhydrochlorid