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Merck
모든 사진(4)

문서

247537

Sigma-Aldrich

Oxalic acid dihydrate

ACS reagent, ≥99%

동의어(들):

Ethanedioic acid dihydrate

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About This Item

Linear Formula:
HO2CCO2H · 2H2O
CAS Number:
Molecular Weight:
126.07
Beilstein:
3679436
EC Number:
MDL number:
UNSPSC 코드:
12352100
eCl@ss:
39021701
PubChem Substance ID:
NACRES:
NA.21

Grade

ACS reagent

Quality Level

vapor density

4.4 (vs air)

vapor pressure

<0.01 mmHg ( 20 °C)

분석

≥99%
99.5-102.5% (ACS specification)

형태

solid

불순물

H2SO4, passes test (darkened)
≤0.001% N compounds
≤0.005% insolubles

무기 잔류물

≤0.01%

mp

104-106 °C (lit.)

음이온 미량물

chloride (Cl-): ≤0.002%
sulfate (SO42-): ≤0.005%

양이온 미량물

Ca: ≤0.001%
Fe: ≤2 ppm
heavy metals: ≤5 ppm (by ICP-OES)

SMILES string

[H]O[H].[H]O[H].OC(=O)C(O)=O

InChI

1S/C2H2O4.2H2O/c3-1(4)2(5)6;;/h(H,3,4)(H,5,6);2*1H2

InChI key

GEVPUGOOGXGPIO-UHFFFAOYSA-N

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일반 설명

Oxalic acid dihydrate is a promising candidate as a phase change material (PCM) for use in thermal energy storage (TES) technology due to its high heat of fusion and energy storage density/price ratio in comparison to other salt hydrates PCMs.

애플리케이션

Oxalic acid dihydrate may be used:
  • As a catalyst in the preparation of tetrahydroquinoline derivatives via imino Diels-Alder reaction.
  • As a homogeneous catalyst in the preparation of highly functionalized piperidines via multi-component reaction.
  • As an oxidant for the formation of triazolinediones from corresponding urazoles and bisurazoles via oxidation.
  • In the transformation of thiols to nitrosothiols by reacting with sodium nitrite.

픽토그램

CorrosionExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

Effects of sodium chloride on the thermal behavior of oxalic acid dihydrate for thermal energy storage
Han L, et al
Applied Energy, 185, 762-767 (2017)
One-pot five-component synthesis of highly functionalized piperidines using oxalic acid dihydrate as a homogenous catalyst.
Sajadikhah SS, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 23(5), 569-572 (2012)
A Convenient Method for the Oxidation of Urazoles to Their Corresponding Triazolinediones Under Mild and Heterogeneous Conditions with Sodium Nitrite and Oxalic Dihydrate.
Zolfigolo MA and Mallakpour SE.
Synthetic Communications, 29(22), 4061-4069 (1999)
An Efficient Method for Production and Storage of Unstable S-Nitrosothiols Under Mild and Heterogeneous Condition with Sodium Nitrite and Oxalic Acid Dihydrate.
Zolfigol MA, et al.
Synthetic Communications, 29(13), 2277-2280 (1999)
Imino Diels-Alder reactions catalyzed by oxalic acid dihydrate. Synthesis of Tetrahydroquinoline derivatives.
Nagarajan R and Perumal PT.
Synthetic Communications, 31(11), 1733-1736 (2001)

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