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675989

Sigma-Aldrich

Cyclopentyl methyl ether

greener alternative

contains 50 ppm BHT as inhibitor, ReagentPlus®, ≥99.90%

Synonym(s):

CPME

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100 μG
₩765,615

₩765,615


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100 μG
₩765,615

About This Item

Empirical Formula (Hill Notation):
C6H12O
CAS Number:
Molecular Weight:
100.16
MDL number:
UNSPSC Code:
12352112
PubChem Substance ID:
NACRES:
NA.21
Bp:
106 °C/760 mmHg

₩765,615


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Quality Level

product line

ReagentPlus®

Assay

≥99.90%

form

liquid

contains

50 ppm BHT as inhibitor

greener alternative product characteristics

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

sustainability

Greener Alternative Product

dilution

(for general lab use)

impurities

≤50 ppm H2O2

bp

106 °C/760 mmHg

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EP3124000040EP3124000091EP3124000083
volume

20 μL

volume

20 μL

volume

200 μL

volume

200 μL

manufacturer/tradename

Eppendorf® 3121000031 (Global)

manufacturer/tradename

Eppendorf® 3121000040 (Global)

manufacturer/tradename

Eppendorf® 3121000090 (Global)

manufacturer/tradename

Eppendorf® 3121000082 (Global)

feature

single-channel, mechanical

feature

single-channel, mechanical

feature

single-channel, mechanical

feature

single-channel, mechanical

packaging

pack of 1 ea

packaging

pack of 1 ea

packaging

pack of 1 ea

packaging

pack of 1 ea

material

gray

material

yellow

material

blue

material

yellow

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. Cyclopentyl methyl ether (CPME) is a greener alternative solvent to many aprotic ether solvents such as tetrahydrofuran (THF), 2-methyl tetrahydrofuran (2-MeTHF), dioxane (carcinogenic), tert-Butyl methyl ether (MTBE), and 1,2-dimethoxyethane (DME) and thus has been enhanced for "Safer Solvents and Auxiliaries".  Click here  for more information.

Application

CPME is a greener alternative solvent and may be used is a broad range of applications such as:

Organic synthesis reactions containing the following reagents and conditions:

  1. Alkali agents
  2. Lewis’s acid-mediated reactions
  3. Organometallic
  4. Reduction and Oxidation
  5. Transition metal catalysts
  6. Azeotropic water removal



Extraction of compounds
Polymer synthesis
Crystallization
Surface coatings

Features and Benefits

  • Synthetic-based sustainable and safer alternative
  • Reduces the number of steps required for production
  • Reduces the amount of water that is required for washing
  • Eliminates the need for co-solvents for product recovery

    It has many properties which make it a safer and greener alternative:
  • Low peroxide formation
  • High boiling point
  • Clean organic-water phase separation
  • Reduced energy to recover

Legal Information

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

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

<37.4 °F - closed cup

Flash Point(C)

< 3 °C - closed cup


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Aaron Black et al.
The journal of gene medicine, 16(5-6), 122-130 (2014-06-26)
Choroideremia (CHM) is a slowly progressive X-linked retinal degeneration that results in a loss of photoreceptors, retinal pigment epithelium and choroid. CHM, the gene implicated in choroideremia, encodes Rab escort protein-1 (REP-1), which is involved in the post-translational activation via
Rafaela Muniz de Queiroz et al.
Cancer investigation, 32(6), 226-235 (2014-04-22)
Current therapies for glioblastoma multiforme (GBM) are not effective. This study investigated the activity of the M. officinalis essential oil (EO) and its major component (citral) in GBM cell lines. Both EO and citral decreased the viability and induced apoptosis

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