8.18766

2-Propanol

≥99.5% (GC), EMPLURA^®

• Synonym(s): sec-Propyl alcohol, IPA, Isopropanol, Isopropyl alcohol
• Linear Formula: (CH₃)₂CHOH
• CAS Number: 67-63-0
• Molecular Weight: 60.10
• Beilstein/REAXYS Number: 635639
• MDL number: MFCD00011674
• UNSPSC Code: 12352104
• EC Index Number: 200-661-7
• NACRES: NB.21

Properties

• product name: 2-Propanol, EMPLURA^®
• vapor density: 2.1 (vs air)
• Quality Level: 200
• 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

Description

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

Safety Information

• pictograms: GHS02,GHS07
• signalword: Danger
• hcodes: H225 - H319 - H336
• pcodes: P210 - P233 - P240 - P241 - P242 - P305 + P351 + P338
• 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