Basic information
- CAS
2122-49-8- Standard SMILES
CC1(C)CC(OP(OC2CC(C)(C)N(O)C(C)(C)C2)OC2CC(C)(C)N(O)C(C)(C)C2)CC(C)(C)N1O- InChIKey
WLGSYBIYACWXFF-UHFFFAOYSA-N- Molecular formula
- C27H54N3O6P
- Average molar mass
- 547.7 g/mol
- Monoisotopic mass
- 547.37502345
Names & identifiers
- Preferred name
- Tris(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl) phosphite
- IUPAC
- tris(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl) phosphite
- English name
- Tri-(4-hydroxy-TEMPO) phosphite
- Molecular formula
- C27H51N3O6P3*
- Molecular weight
- 544.684101
Names & synonyms
2122-49-8tris(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl) phosphiteDTXSID80330392RefChem:386578DTXCID90281487Tri-(4-hydroxy-TEMPO)phosphitetris(2,2,6,6-tetramethyl-1-oxyl-4-piperidyl) phosphiteNSC251799Tri-(4-hydroxy-TEMPO) phosphiteSCHEMBL1557996NSC-251799DS-017774
Show more names
JADEWIN 705Inhibitor705Polymerization inhibitor 705INHIBITOR 705 TRUELICHT IN705High efficiency inhibitor ZJ-705Efficient polymerization inhibitor ZJ-705Tri-(4-hydroxy-TEMPO) phosphite 2122-49-8TH-705 High Efficiency Polymerization Inhibitoris(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl) phosphite
G79498Tris(1-hydroxy-2266-tetramethylpiperidin-4-yl) phosphitePiperidinooxy,2,6,6-tetramethyl-, phosphite (3:1) (ester)1-Piperidinyloxy,4',4''-[phosphinidynetris(oxy)]tris-(2,2,6,6-tetramethyl)-
Properties
Computed structural properties
- XLogP
- 4.1
- Topological polar surface area
- 98.1 Ų
- Hydrogen bond donors
- 3
- Hydrogen bond acceptors
- 9
- Rotatable bonds
- 6
- Heavy atoms
- 37
- Formal charge
- 0
- Complexity
- 659
Physicochemical properties
- Melting point
- 143 °C · 143 °C
- InChI
- InChI=1S/C27H51N3O6P/c1-22(2)13-19(14-23(3,4)28(22)31)34-37(35-20-15-24(5,6)29(32)25(7,8)16-20)36-21-17-26(9,10)30(33)27(11,12)18-21/h19-21H,13-18H2,1-12H3
- InChIKey
- NBEDFLJHKNWIAD-UHFFFAOYSA-N
- SMILES
- P(OC1CC(C)(C)N([O])C(C)(C)C1)(OC1CC(C)(C)N([O])C(C)(C)C1)OC1CC(C)(C)N([O])C(C)(C)C1 |^1:8,20,32|
- CAS DataBase Reference
- 2122 · 2122-49-8
Chemistry & industry
Applications
UsesPolymerization inhibitor 705 can be used as a novel and highly efficient polymerization inhibitor for olefin monomers, acrylates, methacrylates, acrylic acid, acrylonitrile, styrene, butadiene, vinyl chloride, unsaturated polyesters, and other unsaturated compounds, as well as pesticides. Its polymerization inhibition performance is superior to phenols, aromatic amines, ethers, quinones, and nitro compounds. It is suitable for preventing the self-polymerization of olefins and unsaturated monomers during production, separation, purification, storage, and transportation, and for controlling and regulating the degree of polymerization of olefins and their derivatives in organic synthesis reactions.
Suppliers100 total
上海利卡斯实业有限公司19821976800 · [email protected]
湖北永阔科技有限公司027-59223108 15972152991 · [email protected]
湖北万得化工有限公司15377098680 15377098680 · [email protected]
广州纳珑化工有限公司13192879270; 13192879270 · [email protected]
湖北科麦迪化工有限公司18372743325 · [email protected]
杭州景优化工有限公司87211835 13957193240 · [email protected]
河南赢创生物科技有限公司16650615803 · [email protected]
广东百科试剂有限公司13532366769 13686183698 · [email protected]
江西瑞威尔生物科技有限公司18502762009 · [email protected]
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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