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Merck

673773

2-Propanol

greener alternative

≥99.5%, ACS reagent

Sinónimos:

Alcohol sec-propílico, Alcohol isopropílico, IPA, Isopropanol

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About This Item

Fórmula lineal:
(CH3)2CHOH
Número CAS:
67-63-0
Peso molecular:
60.10
UNSPSC Code:
12352001
PubChem Substance ID:
329760563
EC Number:
200-661-7
Beilstein/REAXYS Number:
635639
MDL number:
MFCD00011674
grade:
ACS reagent
assay:
≥99.5%
bp:
82 °C (lit.)
vapor pressure:
33 mmHg ( 20 °C)
44 mmHg ( 25 °C)

Nombre del producto

2-Propanol, ACS reagent, ≥99.5%

SMILES string

CC(C)O

InChI key

KFZMGEQAYNKOFK-UHFFFAOYSA-N

InChI

1S/C3H8O/c1-3(2)4/h3-4H,1-2H3

grade

ACS reagent

vapor density

2.1 (vs air)

vapor pressure

33 mmHg ( 20 °C)
44 mmHg ( 25 °C)

assay

≥99.5%

form

liquid

autoignition temp.

750 °F

expl. lim.

2.0-12.7 %, 93 °C

Quality Level

200

greener alternative product characteristics

Safer Solvents and Auxiliaries
Learn more about the Principles of Green Chemistry.

sustainability

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dilution

(for analytical testing)

impurities

≤0.0001 meq/g Titr. acid or base
≤0.002% carbonyl compounds (propionaldehyde or acetone)
≤0.2% water

evapn. residue

≤0.001%

color

APHA: ≤10

refractive index

n20/D 1.377 (lit.)

pH

7.0 (20 °C)

bp

82 °C (lit.)

mp

−89.5 °C (lit.)

solubility

H2O: passes test
water: soluble

density

0.785 g/mL at 25 °C (lit.)

greener alternative category

Aligned

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Application

2-Propanol may be used in the following processes:
  • As a solvent in the synthesis of di- and trisubstituted ortho biaryls by Suzuki-Miyaura cross-coupling reaction.
  • As an alternate solvent to benzene in the analysis of total carbonyl compounds in heated and frying oils.
  • As a reaction medium in the preparation of cyclic ureas by reacting CO2 with diamines in the presence of pure cerium oxide (CeO2).

General description

2-Propanol (i-PrOH), a renewable secondary alcohol, is water soluble, colorless, volatile liquid with a sweet odor. It is a potential substitute to petroleum-derived gasoline. Preparation of methyl isobutyl ketone (MIBK) using 2-propanol as the precursor has been reported with yield as high as 25%. Solubility of benzoic acid has been investigated in 2-propanol by gravimetric method in the temperature range, 277-346K. Its photocatalytic degradation has been examined by various methods.

Features and Benefits

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This solvent is safe to use and thus aligns with "Safer Solvents and Auxiliaries". Click here for more information.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

Clase de almacenamiento

3 - Flammable liquids

wgk

WGK 1

flash_point_f

53.6 °F - closed cup

flash_point_c

12.0 °C - closed cup

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Certificados de análisis (COA)

Lot/Batch Number
SHBJ6851
SHBH6256
SHBF7667V
SHBG9928V
SHBG3795V

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Visite la Librería de documentos

Influence of activated carbon in TiO2 and ZnO mediated photo-assisted degradation of 2-propanol in gas-solid regime.
Matos J, et al.
Applied Catalysis. B, Environmental, 99(1), 170-180 (2010)
Solubility of benzoic acid in acetone, 2-propanol, acetic acid and cyclohexane: Experimental measurement and thermodynamic modeling.
Long B, et al.
Fluid Phase Equilibria, 297(1), 113-120 (2010)
A modified method for the estimation of total carbonyl compounds in heated and frying oils using 2-propanol as a solvent.
Endo Y, et al.
Journal of the American Oil Chemists' Society, 78(10), 1021-1024 (2001)
A general method for the Suzuki-Miyaura cross-coupling of sterically hindered aryl chlorides: Synthesis of di-and tri-ortho-substituted biaryls in 2-propanol at room temperature.
Navarro O, et al.
Journal of the American Chemical Society, 125(52), 16194-16195 (2003)
Photocatalytic degradation of 2-propanol under irradiation of visible light by nanocrystalline titanium (IV) oxide modified with rhodium ion using adsorption method.
Kitano S, et al.
Chemistry Letters (Jpn), 39(6), 627-629 (2010)
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