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Merck

28-5940

Sigma-Aldrich

Sulfuric acid solution

0.5 M

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About This Item

Fórmula lineal:
H2SO4
Número de CAS:
Peso molecular:
98.08
Beilstein/REAXYS Number:
2037554
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:

form

liquid

availability

available only in Japan

concentration

0.5 M
1 N

SMILES string

OS(O)(=O)=O

InChI

1S/H2O4S/c1-5(2,3)4/h(H2,1,2,3,4)

InChI key

QAOWNCQODCNURD-UHFFFAOYSA-N

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Categorías relacionadas

pictograms

Corrosion

signalword

Warning

hcodes

Hazard Classifications

Met. Corr. 1

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Nucleation of aerosol particles from trace atmospheric vapours is thought to provide up to half of global cloud condensation nuclei. Aerosols can cause a net cooling of climate by scattering sunlight and by leading to smaller but more numerous cloud
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Hepatitis E virus (HEV), a non-enveloped, positive-sense, single-stranded RNA virus, is a major cause of enteric hepatitis. Classified into the family Hepeviridae, HEV comprises four genotypes (genotypes 1-4), which belong to a single serotype. We describe a monoclonal antibody (mAb)
Francesco Riccobono et al.
Science (New York, N.Y.), 344(6185), 717-721 (2014-05-17)
Atmospheric new-particle formation affects climate and is one of the least understood atmospheric aerosol processes. The complexity and variability of the atmosphere has hindered elucidation of the fundamental mechanism of new-particle formation from gaseous precursors. We show, in experiments performed
Andreas Recke et al.
Journal of immunology (Baltimore, Md. : 1950), 193(4), 1600-1608 (2014-07-16)
Subepidermal autoimmune blistering dermatoses (AIBD) are prototypic autoantibody-mediated diseases. In epidermolysis bullosa acquisita (EBA), an autoimmune disease with severe and chronic skin blistering, autoantibodies are directed against type VII collagen. IgG is the predominant autoantibody isotype of EBA, the pathogenicity
Jolan E Walter et al.
The Journal of clinical investigation, 125(11), 4135-4148 (2015-10-13)
Patients with mutations of the recombination-activating genes (RAG) present with diverse clinical phenotypes, including severe combined immune deficiency (SCID), autoimmunity, and inflammation. However, the incidence and extent of immune dysregulation in RAG-dependent immunodeficiency have not been studied in detail. Here

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