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305677

Sigma-Aldrich

tert-Butylphosphonic acid

98%

Synonym(s):

P-(1,1-Dimethylethyl)phosphonic acid

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About This Item

Linear Formula:
(CH3)3CP(O)(OH)2
CAS Number:
4923-84-6
Molecular Weight:
138.10
MDL number:
MFCD00012296
UNSPSC Code:
12352100
PubChem Substance ID:
24858447
NACRES:
NA.22

Assay

98%

mp

187-189 °C (lit.)

SMILES string

CC(C)(C)P(O)(O)=O

InChI

1S/C4H11O3P/c1-4(2,3)8(5,6)7/h1-3H3,(H2,5,6,7)

InChI key

OGDSVONAYZTTDA-UHFFFAOYSA-N

Related Categories

Application

tert-Butylphosphonic acid was used in preparation of:
  • dinuclear dicationic vanadium(IV) complexes
  • borophosphonate cages
  • hexanuclear copper(II) cages
  • soluble molecular copper(II) phosphonates

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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E Fanizza et al.
Nanoscale, 8(6), 3350-3361 (2016-01-15)
Here a luminescent hybrid nanostructure based on functionalized quantum dots (QDs) is used as a fluorescent imaging agent able to target selectively mitochondria thanks to the molecular recognition of the translocator protein (TSPO). The selective targeting of such an 18
Saskia Speed et al.
Inorganic chemistry, 51(12), 6842-6850 (2012-05-26)
The syntheses, structural characterization, and magnetic behavior of two new hexanuclear copper(II) complexes derived from R-phosphonic acids and 1,3-bis(dimethylamino)-2-propanol (Hbdmap) with formulas [Cu(6)(μ-bdmap)(3)(μ(3)-Ph-PO(3))(2)(μ(3)-O···H···μ(3)-O)(ClO(4))(2)(H(2)O)]·5H(2)O (1) and [Cu(6)(μ-bdmap)(3)(μ(3)-t-Bu-PO(3))(2)(μ(3)-O···H···μ(3)-O)(μ(1,3)-dca)(dca)(H(2)O)]·6H(2)O (2) (Ph-H(2)PO(3) = phenylphosphonic acid, t-Bu-H(2)PO(3) = tert-butylphosphonic acid, dca = dicyanamide) are reported.
Pius O Adelani et al.
Inorganic chemistry, 58(19), 12662-12668 (2019-09-13)
We report herein a general synthetic approach for designing uranyl coordination cages. Compounds 1 and 2 are constructed through a temperature-dependent and solvent-driven self-assembly. In both cases, the synthetic strategy involves in situ phosphonate ligand condensation into a flexible pyrophosphonate
Vadapalli Chandrasekhar et al.
Inorganic chemistry, 51(10), 5605-5616 (2012-05-12)
A multicomponent synthetic strategy involving copper(II) ions, tert-butylphosphonic acid (t-BuPO(3)H(2)) and 3-substituted pyrazole ligands has been adopted for the synthesis of soluble molecular copper(II) phosphonates. The use of six different 3-substituted pyrazoles, 3-R-PzH [R = H, Me, CF(3), Ph, 2-pyridyl
Justus Tönnemann et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(32), 9939-9945 (2012-07-06)
A versatile and experimentally facile procedure for the synthesis of borophosphonate cages of the general formula [tBuPO(3)BR'](4) is described. The method involves heating of tert-butylphosphonic acid with a boronic acid in toluene to give borophosphonates in [4+4] condensation reactions. The
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