A6756
Sodium arsenate dibasic heptahydrate
≥98.0%
Sinónimos:
Disodium hydrogen arsenate heptahydrate, di-Sodium hydrogen arsenate heptahydrate
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Fórmula lineal:
Na2HAsO4 · 7H2O
Número CAS:
Peso molecular:
312.01
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
MDL number:
Assay:
≥98.0%
Form:
powder
Servicio técnico
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Permítanos ayudarleQuality Level
assay
≥98.0%
form
powder
reaction suitability
reagent type: catalyst
core: arsenic
pH
8.5-9.0 (25 °C, 50 g/L)
SMILES string
O.O.O.O.O.O.O.[Na+].[Na+].O[As]([O-])([O-])=O
InChI
1S/AsH3O4.2Na.7H2O/c2-1(3,4)5;;;;;;;;;/h(H3,2,3,4,5);;;7*1H2/q;2*+1;;;;;;;/p-2
InChI key
KOLXPEJIBITWIQ-UHFFFAOYSA-L
General description
Sodium arsenate dibasic heptahydrate (As(V)) is an arsenic compound.
Application
Sodium arsenate dibasic heptahydrate may be used as a reference standard for the quantification of arsenic compounds in rice- and seafood-based samples by ion chromatography-inductively coupled plasma/ mass spectrometry. The samples for analysis were prepared by ultrasonic-assisted enzymatic extraction (UAEE).
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1A
Clase de almacenamiento
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Validation of a method for arsenic speciation in food by ion chromatography-inductively coupled plasma/mass spectrometry after ultrasonic-assisted enzymatic extraction.
Dufailly V, et al.
Journal of AOAC (Association of Official Analytical Chemists) International, 94(3), 947-958 (2011)
Shugo Suzuki et al.
Toxicology, 299(2-3), 155-159 (2012-06-06)
Inorganic arsenic is a known human carcinogen, inducing tumors of the skin, urinary bladder and lung. It is metabolized to organic methylated arsenicals. 2,3-Dimercaptopropane-1-sulfonic acid (DMPS), a chelating agent, is capable of reducing pentavalent arsenicals to the trivalent state and
Tatyana S Pinyayev et al.
Chemical research in toxicology, 24(4), 475-477 (2011-03-11)
The conventional scheme for arsenic methylation accounts for methylated oxyarsenical production but not for thioarsenical formation. Here, we report that in vitro anaerobic microbiota of mouse cecum converts arsenate into oxy- and thio- arsenicals. Besides methylarsonic acid (MMA(V)), arsenate was