24-1040

過塩素酸

Name: 過塩素酸
Brand: SAJ
Price: 5910 JPY
Availability: InStock

JIS special grade, 60.0-62.0%

別名:

PCA

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500 G

￥5,910

在庫あり出荷可能詳細

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この商品について

化学式:

HClO₄

CAS番号:

7601-90-3

分子量:

100.46

UNSPSC Code:

12352106

PubChem Substance ID:

329752563

MDL number:

MFCD00011325

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製品名

過塩素酸, JIS special grade, 60.0-62.0%

InChI

1S/ClHO4/c2-1(3,4)5/h(H,2,3,4,5)

SMILES string

OCl(=O)(=O)=O

InChI key

VLTRZXGMWDSKGL-UHFFFAOYSA-N

grade

JIS special grade

form

liquid

reaction suitability

reagent type: oxidant

availability

available only in Japan

concentration

60.0-62.0%

density

154 g/cm³

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当該品目	24-1010	24-1020	24-1050
Sigma-Aldrich 24-1040 Perchloric acid	Sigma-Aldrich 24-1010 Perchloric acid	Sigma-Aldrich 24-1020 Perchloric acid	Sigma-Aldrich 24-1050 Perchloric acid
concentration 60.0-62.0%	concentration 60.0-62.0%	concentration 70.0-72.0%	concentration 60.0-62.0%
grade JIS special grade	grade SAJ super special grade	grade JIS special grade	grade SAJ first grade
form liquid	form liquid	form liquid	form liquid
density 154 g/cm³	density 154 g/cm³	density 167 g/cm³	density 154 g/cm³
reaction suitability reagent type: oxidant	reaction suitability reagent type: oxidant	reaction suitability reagent type: oxidant	reaction suitability reagent type: oxidant
availability available only in Japan	availability available only in Japan	availability available only in Japan	availability available only in Japan

pictograms

GHS03,GHS08,GHS05,GHS07

signalword

Danger

hcodes

H271,H290,H302,H314,H373

pcodes

P210 - P280 - P301 + P330 + P331 - P303 + P361 + P353 - P305 + P351 + P338 + P310 - P314

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Ox. Liq. 1 - Skin Corr. 1A - STOT RE 2

target_organs

Thyroid

保管分類

5.1A - Strongly oxidizing hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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Covalent modification of graphene and graphite using diazonium chemistry: tunable grafting and nanomanipulation.

John Greenwood et al.

ACS nano, 9(5), 5520-5535 (2015-04-22)

We shine light on the covalent modification of graphite and graphene substrates using diazonium chemistry under ambient conditions. We report on the nature of the chemical modification of these graphitic substrates, the relation between molecular structure and film morphology, and

Acid-induced mechanism change and overpotential decrease in dioxygen reduction catalysis with a dinuclear copper complex.

Dipanwita Das et al.

Journal of the American Chemical Society, 135(10), 4018-4026 (2013-02-28)

Catalytic four-electron reduction of O2 by ferrocene (Fc) and 1,1'-dimethylferrocene (Me2Fc) occurs efficiently with a dinuclear copper(II) complex [Cu(II)2(XYLO)(OH)](2+) (1), where XYLO is a m-xylene-linked bis[(2-(2-pyridyl)ethyl)amine] dinucleating ligand with copper-bridging phenolate moiety], in the presence of perchloric acid (HClO4) in

Temperature-independent catalytic two-electron reduction of dioxygen by ferrocenes with a copper(II) tris[2-(2-pyridyl)ethyl]amine catalyst in the presence of perchloric acid.

Dipanwita Das et al.

Journal of the American Chemical Society, 135(7), 2825-2834 (2013-02-12)

Selective two-electron plus two-proton (2e(-)/2H(+)) reduction of O(2) to hydrogen peroxide by ferrocene (Fc) or 1,1'-dimethylferrocene (Me(2)Fc) in the presence of perchloric acid is catalyzed efficiently by a mononuclear copper(II) complex, [Cu(II)(tepa)](2+) (1; tepa = tris[2-(2-pyridyl)ethyl]amine) in acetone. The E(1/2)

How much oxycodone is needed for adequate analgesia after breast cancer surgery: effect of the OPRM1 118A>G polymorphism.

Kristiina Cajanus et al.

The journal of pain : official journal of the American Pain Society, 15(12), 1248-1256 (2014-09-23)

Most clinically used opioids are mu-opioid receptor agonists. Therefore, genetic variation of the OPRM1 gene that encodes the mu-opioid receptor is of great interest for understanding pain management. A polymorphism 118A>G (rs1799971) within the OPRM1 gene results in a missense

In vitro and in vivo multidrug resistance reversal activity by a Betti-base derivative of tylosin.

N Gyémánt et al.

British journal of cancer, 103(2), 178-185 (2010-06-17)

The multidrug resistance (MDR) proteins are present in a majority of human tumours. Their activity is important to understand the chemotherapeutic failure. A search for MDR-reversing compounds was conducted among various Betti-base derivatives of tylosin. Here, we evaluate the in

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