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Merck
CN

415146

Triisopropyl orthoformate

97%

Synonym(s):

2,2′,2′′-[Methylidynetris(oxy)]tris[propane], 2-[Bis(propan-2-yloxy)methoxy]propane, 2-[Di(propan-2-yloxy)methoxy]propane, Tri(2-propyl) orthoformate, Tri(prop-2-yl) orthoformate, Tri-iso-propyl orthoformate, Triisopropyl orthoformate

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About This Item

Linear Formula:
CH[OCH(CH3)2]3
CAS Number:
4447-60-3
Molecular Weight:
190.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24865978
EC Number:
224-688-9
Beilstein/REAXYS Number:
1700668
MDL number:
MFCD00060628
Assay:
97%
Form:
liquid

Key Documents

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InChI key

FPIVAWNGRDHRSQ-UHFFFAOYSA-N

InChI

1S/C10H22O3/c1-7(2)11-10(12-8(3)4)13-9(5)6/h7-10H,1-6H3

SMILES string

CC(C)OC(OC(C)C)OC(C)C

assay

97%

form

liquid

refractive index

n20/D 1.397 (lit.)

bp

65-66 °C/18 mmHg (lit.)

density

0.854 g/mL at 25 °C (lit.)

functional group

ether

Quality Level

200

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Application

Triisopropyl orthoformate may be used for the preparation of 2-(diisopropoxymethyl)oxirane.

General description

Triisopropyl orthoformate (TIPO) is formed during the reaction of dichlorofluoromethane with potassium isopropoxide in isopropyl alcohol. Separation of TIPO from n-hexane by dense carbon nanotube (CNT) membranes by pervaporation has been reported.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

107.6 °F - closed cup

flash_point_c

42 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
00306KJ
10903AJ
11124LQ
09217KF
08723HR

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Miao Yu et al.
Nano letters, 9(1), 225-229 (2008-12-23)
A method is presented to prepare high-density, vertically aligned carbon nanotube (VA-CNT) membranes. The CNT arrays were prepared by chemical vapor deposition (CVD), and the arrays were collapsed into dense membranes by capillary-forces due to solvent evaporation. The average space
Enzymatic Transformations 62. Preparative Scale Synthesis of Enantiopure Glycidyl Acetals using an Aspergillus niger Epoxide Hydrolase-Catalysed Kinetic Resolution.
Doumeche B, et al.
Advanced Synthesis & Catalysis, 348(14), 1948-1957 (2006)
Methylene Derivatives as Intermediates in Polar Reactions. XIX. The Reaction of Potassium Isopropoxide with Chloroform, Bromoform and Dichlorofluoromethane1.
Hine J, et al.
Journal of the American Chemical Society, 82(6), 1398-1401 (1960)

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