243663
Sodium hypophosphite hydrate
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About This Item
Formula condensata:
NaH2PO2 · xH2O
Numero CAS:
Peso molecolare:
87.98 (anhydrous basis)
Numero CE:
Numero MDL:
Codice UNSPSC:
12352300
ID PubChem:
NACRES:
NA.55
Prodotti consigliati
Saggio
~95% (NaH2PO2)
Livello qualitativo
Stato
powder, crystals or chunks
Stringa SMILE
O.[Na+].OP[O-]
InChI
1S/Na.H3O2P.H2O/c;1-3-2;/h;3H2,(H,1,2);1H2/q+1;;/p-1
PLZNPHDJGFDNRM-UHFFFAOYSA-M
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Applicazioni
Sodium hypophosphite hydrate can be used as:
It can also be used to compose the finishing solutions for the immobilization of photo-initiator (benzophenone ) onto cotton fabrics.
- A radical precursor to synthesize mono alkyl phosphinic acids via radical reaction with alkenes in the presence of Et3B as the initiator.
- A reagent for the reduction of the diazonium salt.
- A hydrogen donor in the transfer-hydrogenation reactions.
- A catalyst in the esterification reaction.
It can also be used to compose the finishing solutions for the immobilization of photo-initiator (benzophenone ) onto cotton fabrics.
Sodium hypophosphite hydrate is widely used as an esterification catalyst. It may be used to compose the finishing solutions for the incorporation of benzophenone (photoinitiator) onto cotton fabrics.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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UV-induced graft polymerization of acrylamide on cellulose by using immobilized benzophenone as a photo-initiator.
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European Polymer Journal, 45(8), 2443-2449 (2009)
X-Ray Photoelectron Spectroscopy of Lignocellulosic Materials Treated with Malea Ted Polypropylenes
Kazayawoko M, et al.
J. Wood Chem. Technol., 18(1), 1-26 (1998)
S Deprèle et al.
The Journal of organic chemistry, 66(20), 6745-6755 (2001-10-02)
A novel and practical approach to monosubstituted phosphinic acid (alkylphosphonous acid) derivatives from hypophosphite salts or esters is described. Phosphorus-centered radical formation is initiated with Et(3)B/O(2), and the reaction is conveniently conducted at room temperature in an open flask. In
Photoactive antibacterial cotton fabrics treated by 3, 3', 4, 4'-benzophenonetetracarboxylic dianhydride.
Hong KH and Sun G.
Carbohydrate Polymers, 84(3), 1027-1032 (2011)
Photocatalytic functional cotton fabrics containing benzophenone chromophoric groups.
Hong KH and Sun G.
Journal of Applied Polymer Science, 106(4), 2661-2667 (2007)
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