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주요 문서

222283

Sigma-Aldrich

Magnesium perchlorate

ACS reagent

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100 ML
$156.00
500 ML
$676.00

$156.00


출고 가능일April 03, 2025세부사항


벌크 견적 요청

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100 ML
$156.00
500 ML
$676.00

About This Item

Linear Formula:
Mg(ClO4)2
CAS Number:
Molecular Weight:
223.21
EC Number:
MDL number:
UNSPSC 코드:
12352300
PubChem Substance ID:
NACRES:
NB.24

$156.00


출고 가능일April 03, 2025세부사항


벌크 견적 요청

Grade

ACS reagent

양식

flakes
powder, chunks or granules

반응 적합성

reagent type: oxidant

농도

>10% Mg (EDTA titration)

불순물

≤0.005 meq/g Titr. free acid
≤0.025 meq/g Titr. base

손실

≤8% loss on drying

적합성

passes test for moisture absorption

SMILES string

[Mg++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O

InChI

1S/2ClHO4.Mg/c2*2-1(3,4)5;/h2*(H,2,3,4,5);/q;;+2/p-2

InChI key

MPCRDALPQLDDFX-UHFFFAOYSA-L

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유사한 품목 비교

전체 비교 보기

차이점 표시

1 of 4

이 품목
74738CRM78295O806
1-Octadecene ≥95.0% (GC)

74740

1-Octadecene

1-Octadecene analytical standard, ≥99.0% (GC)

74738

1-Octadecene

1-Octadecene technical grade, 90%

O806

1-Octadecene

Quality Level

100

Quality Level

100

Quality Level

300

Quality Level

100

bp

314.4 +/- 5.0 °C/760 mmHg (lit.), 314.4 °C±5.0 °C/760 mmHg (lit.), 179 °C/15 mmHg (lit.)

bp

179 °C/15 mmHg (lit.), 314.4 °C±5.0 °C/760 mmHg (lit.)

bp

179 °C/15 mmHg (lit.), 314.4 °C±5.0 °C/760 mmHg (lit.)

bp

314.4 +/- 5.0 °C/760 mmHg (lit.), 179 °C/15 mmHg (lit.), 314.4 °C±5.0 °C/760 mmHg (lit.)

refractive index

n20/D 1.444 (lit.), n20/D 1.445

refractive index

n20/D 1.444 (lit.), n20/D 1.445

refractive index

n20/D 1.444 (lit.)

refractive index

n20/D 1.444 (lit.)

form

liquid

form

-

form

-

form

-

density

0.789 g/mL at 25 °C (lit.)

density

0.789 g/mL at 25 °C (lit.)

density

0.789 g/mL at 25 °C (lit.)

density

0.789 g/mL at 25 °C (lit.)

일반 설명

Magnesium perchlorate (Mg(ClO4)2) is widely used as drying agent for gases. It can remove water from gases (with no organic contaminants) at the rate of 0.001mgwater/l.[1]

애플리케이션

Magnesium perchlorate (Mg(ClO4)2) may be employed as a catalyst in the following studies:
  • Preparation of α-aminophosphonates.[2]
  • Enantioselective Diels-Alder reaction between cyclopentadiene and 3-acryloyl-1,3-oxazolin-2-one.[3]
  • Preparation of imines and phenylhydrazones.[4]
  • Protection of alcohols in the form of t-butyl ethers.[5]
Magnesium perchlorate may be used as a catalyst in the synthesis of the following compounds:
  • α-Aminophosphonates via three-component reaction between an amine, an aldehyde or a ketone and a di-/trialkyl phosphite.[2]
  • Imines and phenylhydrazones by the condensation of carbonyl compounds with amines and phenylhydrazine.[4]
  • Knoevenagel adducts via Knoevenagel condensation between β-diketones and aliphatic or aromatic aldehydes.[6]
It may also be used to catalyze the protection of alcohols as t-butyl ethers.[5]

픽토그램

Flame over circleExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Ox. Sol. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

5.1A - Strongly oxidizing hazardous materials

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

Magnesium perchlorate as efficient Lewis acid for the Knoevenagel condensation between ?-diketones and aldehydes.
Bartoli G, et al.
Tetrahedron Letters, 49(16), 2555-2557 (2008)
Magnesium perchlorate as an efficient catalyst for the synthesis of imines and phenylhydrazones.
Chakraborti AK, et al.
Tetrahedron Letters, 45(41), 7641-7644 (2004)
Eagleson M.
Concise Encyclopedia Chemistry, 343-343 (1994)
The first enantioselective synthesis of both Diels-Alder enantiomers with the same bis (oxazoline)-magnesium perchlorate chiral catalyst.
Desimoni G, et al.
Tetrahedron Letters, 37(17), 3027-3030 (1996)
F Javier Céspedes-Guirao et al.
The Journal of organic chemistry, 74(16), 5871-5880 (2009-07-29)
Zinc phthalocyanine-perylenebisimide pentameric arrays, ZnPc(PDI)(4) 1 and 2, have been synthesized. ZnPc(PDI)(4) 1 has no substituents in the PDI bay positions, while ZnPc(PDI)(4) 2 presents four phenoxy groups in the bay positions of each perylene. In both cases, the PDI

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