03366
Phosphate atomic spectroscopy standard concentrate 1.00 g PO43-
1.00 g/L, for 1L standard solution, analytical standard
Synonym(s):
Phosphoric acid solution
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About This Item
Linear Formula:
H3PO4
CAS Number:
Molecular Weight:
98.00
PubChem Substance ID:
UNSPSC Code:
41116107
Beilstein/REAXYS Number:
1921286
MDL number:
SMILES string
OP(O)(O)=O
InChI
1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)
InChI key
NBIIXXVUZAFLBC-UHFFFAOYSA-N
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
packaging
ampule of
concentration
1.00 g/L
solubility
H2O: soluble
format
single component solution
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General description
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.
Preparation Note
prepared with H3PO4 and H2O
signalword
Warning
hcodes
pcodes
Hazard Classifications
Met. Corr. 1
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles
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Alessio Ciulli et al.
Journal of medicinal chemistry, 49(16), 4992-5000 (2006-08-04)
Mapping interactions at protein-ligand binding sites is an important aspect of understanding many biological reactions and a key part of drug design. In this paper, we have used a fragment-based approach to probe "hot spots" at the cofactor-binding site of
Alex W Gregory et al.
Organic letters, 15(17), 4330-4333 (2013-08-30)
A highly enantioselective hydroamination/N-sulfonyliminium cyclization cascade is reported using a combination of gold(I) and chiral phosphoric acid catalysts. An initial 5-exo-dig hydroamination and a subsequent phosphoric acid catalyzed cyclization process provide access to complex sulfonamide scaffolds in excellent yield and
W M Fennis et al.
Journal of dental research, 93(1), 36-41 (2013-10-25)
The objective of this randomized control trial was to compare the five-year clinical performance of direct and indirect resin composite restorations replacing cusps. In 157 patients, 176 restorations were made to restore maxillary premolars with Class II cavities and one
Li Yan Chan et al.
The Journal of organic chemistry, 78(17), 8826-8832 (2013-08-07)
A simple and efficient method is developed for Pd-catalyzed ortho-acetoxylation using organophosphates, namely, benzylic phosphonic and aryl phosphoric monoacids, as the directing group.
Keiji Mori et al.
Journal of the American Chemical Society, 135(10), 3964-3970 (2013-02-19)
Described herein is the enantioselective synthesis of multisubstituted biaryl derivatives by chiral phosphoric acid catalyzed asymmetric bromination. Two asymmetric reactions (desymmetrization and kinetic resolution) proceeded successively to afford chiral biaryls in excellent enantioselectivities (up to 99% ee). Both experimental and
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