698822
Phosphoric acid solution
suitable for NMR (reference standard), 85% in D2O (99.9 atom % D), NMR tube size 5 mm × 8 in.
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Fórmula lineal:
H3PO4
Número CAS:
Peso molecular:
98.00
UNSPSC Code:
12352106
NACRES:
NA.12
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1921286
Assay:
83.5-86.5% (gravimetric)
Concentration:
85% in D2O (99.9 atom % D)
Form:
solution
Servicio técnico
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Permítanos ayudarleassay
83.5-86.5% (gravimetric)
Quality Level
form
solution
concentration
85% in D2O (99.9 atom % D)
technique(s)
NMR: suitable
NMR tube size
5 mm × 8 in.
density
1.481 g/cm3
suitability
suitable for NMR (reference standard)
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
Features and Benefits
31P sensitivity
Preparation Note
5 mm O.D. tube contains 0.700 mL.
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Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Clase de almacenamiento
8B - Non-combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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.