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Merck
CN

04420

Phosphinic acid

puriss., meets analytical specification of NF, 30-32%

Synonym(s):

Hypophosphorous acid

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About This Item

Linear Formula:
H3PO2
CAS Number:
Molecular Weight:
66.00
UNSPSC Code:
12352106
PubChem Substance ID:
MDL number:
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grade

puriss.

quality

meets analytical specification of NF

concentration

30-32%

impurities

≤0.002% heavy metals (as Pb)

density

1.206 g/mL at 20 °C (lit.)

anion traces

chloride (Cl-): ≤200 mg/kg, sulfate (SO42-): ≤200 mg/kg

cation traces

As: ≤1 mg/kg, Ca: ≤50 mg/kg, Cu: ≤5 mg/kg, Fe: ≤20 mg/kg, Na: ≤1000 mg/kg

SMILES string

O[PH2]=O

InChI

1S/H3O2P/c1-3-2/h3H2,(H,1,2)

InChI key

ACVYVLVWPXVTIT-UHFFFAOYSA-N

General description

Phosphinic acid is a reagent containing P-H bond. Phosphinic acids (phosphinates) are the derivatives of phosphinic acid H2P(O)(OH). Biochemical, biological, and medical applications of phosphinic acid compounds have been evaluated. Natural products containing carbon-phosphorus bonds (phosphonic and phosphinic acids) have wide applications in medicine and agriculture. Phosphinic acids have been synthesized via Michael addition of phosphonous acids as well as esters to activated conjugated systems. Phosphinic acid (Hypophosphorous acid) is an effective radical reducing agent for organic halides, thionoesters and isocyanides.


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William W Metcalf et al.
Annual review of biochemistry, 78, 65-94 (2009-06-06)
Natural products containing carbon-phosphorus bonds (phosphonic and phosphinic acids) have found widespread use in medicine and agriculture. Recent years have seen a renewed interest in the biochemistry and biology of these compounds with the cloning of the biosynthetic gene clusters
Preparation of phosphinic acids: Michael additions of phosphonous acids/esters to conjugated systems.
Thottathil JK, et al.
Tetrahedron Letters, 25(42), 4741-4744 (1984)
The invention of radical reactions. Part 32. Radical deoxygenations, dehalogenations, and deaminations with dialkyl phosphites and hypophosphorous acid as hydrogen sources.
Barton DHR, et al.
The Journal of Organic Chemistry, 58(24), 6838-6842 (1993)



Global Trade Item Number

SKUGTIN
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