Skip to Content
Merck
All Photos(5)

Documents

215112

Sigma-Aldrich

Phosphorous acid

99%

Synonym(s):

Phosphonic acid

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
H3O3P
CAS Number:
Molecular Weight:
82.00
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.21

Quality Level

Assay

99%

form

crystals or chunks
flakes

solubility

water: soluble

density

1.651 g/mL at 25 °C (lit.)

SMILES string

[H]P(O)(O)=O

InChI

1S/H3O3P/c1-4(2)3/h4H,(H2,1,2,3)

InChI key

ABLZXFCXXLZCGV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Phosphorous acid (or phosphonic acid) is a phosphorus oxoacid commonly used as an intermediate in chemical synthesis for the production of various phosphorus compounds. It is also used as a strong reducing agent in organic synthesis.

Application

Phosphorous acid (H3PO3, orthophosphorous acid) may be used as one of the reaction components for the synthesis of the following:
  • α-aminomethylphosphonic acids via Mannich-Type Multicomponent Reaction
  • 1-aminoalkanephosphonic acids via amidoalkylation followed by hydrolysis
  • N-protected α-aminophosphonic acids (phospho-isosteres of natural amino acids) via amidoalkylation reaction

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Amidoalkylation of phosphorous acid.
Vinyukov AV, et al.
Russ. J. Gen. Chem., 85(2), 366-369 (2015)
Ping Yin et al.
Bioresource technology, 110, 258-263 (2012-02-22)
Esterification of oleic acid with ethanol catalyzed by organophosphonic acid-functionalized silica SG-T-P was optimized using response surface methodology (RSM). The interactive effect of catalyst to FFA weight ratio and molar ratio of alcohol to acid were more significant than that
Emily B Pentzer et al.
Advanced materials (Deerfield Beach, Fla.), 24(17), 2254-2258 (2012-03-28)
Poly(3-hexyl thiophene) containing chain-end thiols or phosphonic acids is crystallized to yield nanowires with the functional groups at the wire edges. CdSe quantum dots and nanorods associate with these fibrils, leading to 'superhighways' that consist of alternating parallel lanes of
L Qi et al.
Langmuir : the ACS journal of surfaces and colloids, 28(31), 11448-11456 (2012-07-17)
In a recent publication, we have highlighted the potential of phosphonic acid terminated PEG oligomers to functionalize strong UV absorption cerium oxide nanoparticles, which yield suspensions that are stable in aqueous or organic solvents and are redispersible in different solvents
Alain Graillot et al.
Journal of hazardous materials, 244-245, 507-515 (2012-11-28)
In order to remove metal ions from wastewaters, thermosensitive copolymers bearing sorption properties toward metal cations were prepared by free radical copolymerization between the N-n-propylacrylamide (NnPAAm) and the (dimethoxyphosphoryl)methyl 2-methylacrylate (MAPC1), followed by a hydrolysis of the phosphonated esters into

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service