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Merck

723320

Magnesium

in a Sure/Seal bottle, turnings, anhydrous tetrahydrofuran 37.5 mmol

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제품정보 (DICE 배송 시 비용 별도)

실험식(Hill 표기법):
Mg
CAS 번호:
Molecular Weight:
24.31
UNSPSC Code:
12352300
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4948473
Form:
turnings
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vapor pressure

1 mmHg ( 621 °C)

Quality Level

form

turnings

autoignition temp.

950 °F

composition

anhydrous tetrahydrofuran, 37.5 mmol

reaction suitability

reagent type: reductant

resistivity

4.46 μΩ-cm, 20°C

bp

1090 °C (lit.)

mp

648 °C (lit.)

density

1.74 g/mL at 25 °C (lit.)

SMILES string

[Mg]

InChI

1S/Mg

InChI key

FYYHWMGAXLPEAU-UHFFFAOYSA-N

Application

Magnesium turnings (Mg) can be used to prepare reactive organomagnesium compounds (Grignard reagents, GR) by reacting with alkyl, allyl, vinyl, or aryl halides. These GR reagents are widely used in organic synthesis to produce useful chemical intermediates. Mg can also be used to prepare tetraisopropyl- and tetrabutyl-distibane by dehalogenation of diisopropyl- and dibutyl-antinomy bromide, respectively.

Other Notes

Based on preparing 0.5 M solution of organomagnesium reagent and 40% headspace.

Legal Information

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC


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Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Self-heat. 1 - STOT SE 3

target_organs

Respiratory system

supp_hazards

저장 등급

4.2 - Pyrophoric and self-heating hazardous materials

wgk

WGK 1

flash_point_f

1.4 °F - closed cup

flash_point_c

-17.0 °C - closed cup



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시험 성적서(COA)

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문서 라이브러리 방문



Reduktion von isopropyl-und butylantimonbromiden mit magnesium
Breunig HJ and KW
Journal of Organometallic Chemistry, 186(1), C5-C8 (1980)
Titanium-magnesium-assisted scission of 1, 4-bis (trimethylsilyl)-1, 3-butadiyne: synthesis and structure of a titanium (III) tweezer complex,[(. eta. 5-C5HMe4) 2Ti (. eta. 1-C. tplbond. CSiMe3) 2][Mg (THF) Cl]
Troyanov SI, et al.
Organometallics, 12(7), 2820-2824 (1993)
Mechanical activation of magnesium turnings for the preparation of reactive Grignard reagents
Baker KV, et al.
The Journal of Organic Chemistry, 56(2), 698-703 (1991)