Diisopropyl ether information

Diisopropyl ether
Names
	Preferred IUPAC name 2-[(Propan-2-yl)oxy]propane
	Other names Isopropyl ether; 2-Isopropoxypropane; Diisopropyl oxide; DIPE
Identifiers
CAS Number	108-20-3 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL3185565;
ChemSpider	7626 ;
ECHA InfoCard	100.003.237
EC Number	203-560-6;
PubChem CID	7914;
RTECS number	TZ5425000;
UNII	DO7Y998826 ;
UN number	1159
CompTox Dashboard (EPA)	DTXSID4021890 ;
	InChI InChI=1S/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3 Key: ZAFNJMIOTHYJRJ-UHFFFAOYSA-N ; InChI=1/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3 Key: ZAFNJMIOTHYJRJ-UHFFFAOYAC;
	SMILES O(C(C)C)C(C)C;
Properties
Chemical formula	C6H14O
Molar mass	102.177 g·mol−1
Appearance	Colorless liquid
Odor	Sharp, sweet, ether-like
Density	0.725 g/ml
Melting point	−60 °C (−76 °F; 213 K)
Boiling point	68.5 °C (155.3 °F; 341.6 K)
Solubility in water	2 g/L at 20 °C
Vapor pressure	119 mmHg (20°C)
Magnetic susceptibility (χ)	-79.4·10−6 cm3/mol
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H225, H316, H319, H335, H336, H361, H371, H412
Precautionary statements	P201, P202, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P273, P280, P281, P303+P361+P353, P304+P340, P305+P351+P338, P308+P313, P309+P311, P312, P332+P313, P337+P313, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)	1 3 1
Flash point	−28 °C (−18 °F; 245 K)
Autoignition; temperature	443 °C (829 °F; 716 K)
Explosive limits	1.4–7.9%
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	8470 mg/kg (rat, oral)
LDLo (lowest published)	5000-6500 mg/kg (rabbit, oral)
LC50 (median concentration)	38,138 ppm (rat); 30,840 ppm (rabbit); 28,486 ppm (rabbit)
	NIOSH (US health exposure limits):
PEL (Permissible)	TWA 500 ppm (2100 mg/m3)
REL (Recommended)	TWA 500 ppm (2100 mg/m3)
IDLH (Immediate danger)	1400 ppm
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Diisopropyl ether is a secondary ether that is used as a solvent. It is a colorless liquid that is slightly soluble in water, but miscible with organic solvents. It is used as an extractant and an oxygenate gasoline additive. It is obtained industrially as a byproduct in the production of isopropanol by hydration of propylene.^[3] Diisopropyl ether is sometimes represented by the abbreviation DIPE.

^ ^a ^b ^c ^d ^e NIOSH Pocket Guide to Chemical Hazards. "#0362". National Institute for Occupational Safety and Health (NIOSH).
^ ^a ^b ^c "Isopropyl ether". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
^ Sakuth, Michael; Mensing, Thomas; Schuler, Joachim; Heitmann, Wilhelm; Strehlke, Günther; Mayer (2010). "Ethers, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_023.pub2. ISBN 978-3527306732.

[NIOSH-1] NIOSH Pocket Guide to Chemical Hazards. "#0362". National Institute for Occupational Safety and Health (NIOSH).

[IDLH-2] "Isopropyl ether". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).

[Ullmann-3] Sakuth, Michael; Mensing, Thomas; Schuler, Joachim; Heitmann, Wilhelm; Strehlke, Günther; Mayer (2010). "Ethers, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_023.pub2. ISBN 978-3527306732.

Diisopropyl ether information

and 26 Related for: Diisopropyl ether information

Diisopropyl ether

Dimethyl ether

Isopropyl alcohol

C6H14O

Oxygenate

Solvent

Ineos

Azeotrope tables

List of cooling baths

Astatine

Flammability limit

Acetone peroxide

List of gasoline additives

IPE

Hydroperoxide

List of UN numbers 1101 to 1200

Diethylaluminium cyanide

Lithium diisopropylamide

List of compounds with carbon number 6

Tipiracil

Trifluoroacetyl chloride

MOSCED

IARC group 2B

Mitsunobu reaction

Retinyl palmitate

Diafenthiuron

Names

Preferred IUPAC name 2-[(Propan-2-yl)oxy]propane
Other names Isopropyl ether 2-Isopropoxypropane Diisopropyl oxide DIPE
Identifiers
CAS Number	108-20-3^Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL3185565
ChemSpider	7626^Y
ECHA InfoCard	100.003.237
EC Number	203-560-6
PubChem CID	7914
RTECS number	TZ5425000
UNII	DO7Y998826^Y
UN number	1159
CompTox Dashboard (EPA)	DTXSID4021890
InChI InChI=1S/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3^Y Key: ZAFNJMIOTHYJRJ-UHFFFAOYSA-N^Y InChI=1/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3 Key: ZAFNJMIOTHYJRJ-UHFFFAOYAC
SMILES O(C(C)C)C(C)C
Properties
Chemical formula	C₆H₁₄O
Molar mass	102.177 g·mol⁻¹
Appearance	Colorless liquid
Odor	Sharp, sweet, ether-like^[1]
Density	0.725 g/ml
Melting point	−60 °C (−76 °F; 213 K)
Boiling point	68.5 °C (155.3 °F; 341.6 K)
Solubility in water	2 g/L at 20 °C
Vapor pressure	119 mmHg (20°C)^[1]
Magnetic susceptibility (χ)	-79.4·10⁻⁶ cm³/mol
Hazards
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H225, H316, H319, H335, H336, H361, H371, H412
Precautionary statements	P201, P202, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P273, P280, P281, P303+P361+P353, P304+P340, P305+P351+P338, P308+P313, P309+P311, P312, P332+P313, P337+P313, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)	1 3 1
Flash point	−28 °C (−18 °F; 245 K)
Autoignition temperature	443 °C (829 °F; 716 K)
Explosive limits	1.4–7.9%
Lethal dose or concentration (LD, LC):
LD₅₀ (median dose)	8470 mg/kg (rat, oral)^[2]
LD_Lo (lowest published)	5000-6500 mg/kg (rabbit, oral)^[2]
LC₅₀ (median concentration)	38,138 ppm (rat) 30,840 ppm (rabbit) 28,486 ppm (rabbit)^[2]
NIOSH (US health exposure limits):
PEL (Permissible)	TWA 500 ppm (2100 mg/m³)^[1]
REL (Recommended)	TWA 500 ppm (2100 mg/m³)^[1]
IDLH (Immediate danger)	1400 ppm^[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references