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方案
~95% (NaH2PO2)
表单
powder, crystals or chunks
SMILES字符串
O.[Na+].OP[O-]
InChI
1S/Na.H3O2P.H2O/c;1-3-2;/h;3H2,(H,1,2);1H2/q+1;;/p-1
InChI key
PLZNPHDJGFDNRM-UHFFFAOYSA-M
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应用
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.[5]
- A radical precursor to synthesize mono alkyl phosphinic acids via radical reaction with alkenes in the presence of Et3B as the initiator.[1]
- A reagent for the reduction of the diazonium salt.[2]
- A hydrogen donor in the transfer-hydrogenation reactions.[3]
- A catalyst in the esterification reaction.[4]
It can also be used to compose the finishing solutions for the immobilization of photo-initiator (benzophenone ) onto cotton fabrics.[5]
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Effect of wood filler treatment and EBAGMA compatibilizer on morphology and mechanical properties of low density polyethylene/olive husk flour composites.
Kaci M, et al.
Express Polymer Letters, 1(7), 467-473 (2007)
Convenient synthesis of 4-methylhistamine and racemic. alpha., 4-dimethylhistamine and. alpha., 4-dimethylhistidine
Davey DD and Lumma Jr WC
The Journal of Organic Chemistry, 54(13), 3211-3213 (1989)
Chlorination of aniline and methyl carbanilate by N-chlorosuccinimide and synthesis of 1, 3, 5-trichlorobenzene
Davis Matthew C
Synthetic Communications, 39(6), 1100-1108 (2009)
Photoactive antibacterial cotton fabrics treated by 3, 3', 4, 4'-benzophenonetetracarboxylic dianhydride.
Hong KH and Sun G.
Carbohydrate Polymers, 84(3), 1027-1032 (2011)
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
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