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675431

Sigma-Aldrich

2-Propanol

99.9%, HPLC Plus, for residue analysis, suitable for gas chromatography (GC) and HPLC, poly coated bottles

Synonym(s):

sec-Propyl alcohol, IPA, Isopropanol, Isopropyl alcohol

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About This Item

Linear Formula:
(CH3)2CHOH
CAS Number:
Molecular Weight:
60.10
Beilstein:
635639
EC Number:
MDL number:
UNSPSC Code:
12190000
PubChem Substance ID:

product name

2-Propanol, HPLC Plus, for HPLC, GC, and residue analysis, 99.9%, poly coated bottles

grade

HPLC Plus
for residue analysis

Quality Level

vapor density

2.1 (vs air)

vapor pressure

33 mmHg ( 20 °C)
44 mmHg ( 25 °C)

Assay

99.9%

form

liquid

autoignition temp.

750 °F

expl. lim.

2.0-12.7 %, 93 °C

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤0.02% water
water

evapn. residue

≤0.0001%

color

colorless

refractive index

n20/D 1.377 (lit.)

bp

82 °C (lit.)

mp

−89.5 °C (lit.)

solubility

water: soluble

density

0.785 g/mL at 25 °C (lit.)

UV absorption

λ: 245 nm Amax: ≤1.0
λ: 250 nm Amax: ≤0.30
λ: 275 nm Amax: ≤0.005
λ: 400 nm Amax: ≤0.005

application(s)

food and beverages

SMILES string

CC(C)O

InChI

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

InChI key

KFZMGEQAYNKOFK-UHFFFAOYSA-N

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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.

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).

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Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

53.6 °F - closed cup

Flash Point(C)

12.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Alcohols
Hazardous rank II

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

675431-4L:4548173239613
675431-VAR:
675431-BULK:
675431-4X4L:4548173239620


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Customers Also Viewed

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)
Highly efficient synthesis of cyclic ureas from CO2 and diamines by a pure CeO2 catalyst using a 2-propanol solvent.
Tamura M, et al.
Green Chemistry, 15(6), 1567-1577 (2013)
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)
Photocatalytic degradation of 2-propanol and phenol using Au loaded MnWO4 nanorod under visible light irradiation.
Chakraborty AK, et al.
Journal of Cluster Science, 23(2), 437-448 (2012)

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