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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

Sinônimo(s):

Álcool sec-propílico, IPA, Isopropanol, Álcool isopropílico

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About This Item

Fórmula linear:
(CH3)2CHOH
Número CAS:
Peso molecular:
60.10
Beilstein:
635639
Número CE:
Número MDL:
Código UNSPSC:
12190000
ID de substância PubChem:

product name

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

grau

HPLC Plus
for residue analysis

Nível de qualidade

densidade de vapor

2.1 (vs air)

pressão de vapor

33 mmHg ( 20 °C)
44 mmHg ( 25 °C)

Ensaio

99.9%

forma

liquid

temperatura de autoignição

750 °F

Lim. expl.

2.0-12.7 %, 93 °C

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

Impurezas

≤0.02% water
water

resíduo de evaporação

≤0.0001%

cor

colorless

índice de refração

n20/D 1.377 (lit.)

pb

82 °C (lit.)

pf

−89.5 °C (lit.)

solubilidade

water: soluble

densidade

0.785 g/mL at 25 °C (lit.)

Absorção UV

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

aplicação(ões)

food and beverages

cadeia de caracteres SMILES

CC(C)O

InChI

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

chave InChI

KFZMGEQAYNKOFK-UHFFFAOYSA-N

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Categorias relacionadas

Descrição geral

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.

Aplicação

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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Pictogramas

FlameExclamation mark

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

53.6 °F - closed cup

Ponto de fulgor (°C)

12.0 °C - closed cup

Equipamento de proteção individual

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


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Supelco

1.00998

2-propanol

2-propanol United States Pharmacopeia (USP) Reference Standard

USP

1570428

2-propanol

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)
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)
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)
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)

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