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8.18766

Supelco

2-Propanol

≥99.5% (GC), EMPLURA®

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Synonym(s):
sec-Propyl alcohol, IPA, Isopropanol, Isopropyl alcohol
Linear Formula:
(CH3)2CHOH
CAS Number:
Molecular Weight:
60.10
Beilstein/REAXYS Number:
635639
MDL number:
UNSPSC Code:
12352104
EC Index Number:
200-661-7
NACRES:
NB.21

vapor density

2.1 (vs air)

Quality Level

vapor pressure

33 mmHg ( 20 °C)
43 hPa ( 20 °C)
44 mmHg ( 25 °C)

product line

EMPLURA®

assay

≥99.5% (GC)

form

liquid

autoignition temp.

750 °F

potency

5045 mg/kg LD50, oral (Rat)
12800 mg/kg LD50, skin (Rabbit)

expl. lim.

2.0-12.7 %, 93 °C

impurities

≤0.2% Water

evapn. residue

≤0.0020%

refractive index

n20/D 1.377 (lit.)

pH

7 (20 °C)

bp

82 °C (lit.)

mp

−89.5 °C (lit.)

transition temp

flash point 12 °C

density

0.785 g/mL at 25 °C (lit.)

storage temp.

2-25°C

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

EMPLURA® is our low-cost alternative to high-purity qualities. With EMPLURA we offer a range of solvents for a plurality of basic applications in non-regulated industries and for less demanding applications, preparative laboratory work and cleaning purposes. EMPLURA solvents provide adequate specifications with the most important parameters.

Application


  • Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones.: The study showcases the role of 2-propanol in asymmetric catalysis, providing an efficient method for the stereoselective hydrogenation of ketones, which is vital in pharmaceutical synthesis (Noyori and Ohkuma, 2001).

  • Electrospray ionization mass spectrometry of synthetic oligonucleotides using 2-propanol and spermidine.: This research examines the use of 2-propanol in electrospray ionization mass spectrometry, enhancing the detection and analysis of synthetic oligonucleotides (De Bellis et al., 2000).

  • Isolation, identification, and chemical synthesis of 8 alpha,25-dihydroxy-9,10-seco-4,6,10(19)-cholestatrien-3-one. A new metabolite of 25-hydroxyvitamin D3 produced by mouse myeloid leukemia cells (M1).: This study details the use of 2-propanol in the chemical synthesis of a new vitamin D3 metabolite, which is significant for understanding vitamin D metabolism in leukemia cells (Yamada et al., 1987).

Analysis Note

Purity (GC): ≥ 99.5 %
Identity (IR): conforms
Density (d 20 °C/ 4 °C): 0.784 - 0.785
Evaporation residue: ≤ 0.0020 %
Water: ≤ 0.20 %

Legal Information

EMPLURA is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

53.6 °F - closed cup

flash_point_c

12.0 °C - closed cup


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