| Identification | More | [Name]
[3-(Dimethylamino)propyl]triphenylphosphonium bromide hydrobromide | [CAS]
27710-82-3 | [Synonyms]
(3-DIMETHYLAMINOPROPYL)TRIPHENYLPHOSPHONIUM BROMIDE HYDROBROMIDE
PHOSPHONIUM, [3-(DIMETHYLAMINO)PROPYL]TRIPHENYL BROMIDE HYDROBROMIDE
(3-dimethylaminopropyl)triphenylphospho-nium brom.hydrobromi
PHOSPHONIUM,[3-(DIMETHYLAMINO)PROPYL]TRIPHENYL BROMIDE HBr
[3-(Dimethylamino)propyl]triphenyl bromide hydrobromide
(3-DIMETHYLAMINOPROPYL)-TRIPHENYL-PHOSPH
forOlopatadine
PHOSPHONIUM, [3-(DIMETHYLAMINO)PROPYL]TRIPHENYL BROMIDE HYDROBROMIDE (FOR OLOPATADINE)
[3-(Dimethylamino)propyl] triphenylphosphonium bromide hydrobromide ( For Olopatadine )
[3-(Dimethylamino)propyl]triphenylphosphonium bromide hydrobromide (Olopatadine)
(3-DIMETHYLAMINOPROPYL)TRIPHENYLPHOSPHONIUM BROMIDE HYDROBROMIDE 98%
(3-DIMETHYLAMINOPROPYL)TRIPHENYLPHOSPHONIUM BROMIDE HBR | [EINECS(EC#)]
608-135-2 | [Molecular Formula]
C23H28Br2NP | [MDL Number]
MFCD00077740 | [Molecular Weight]
509.26 | [MOL File]
27710-82-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
283-285 °C
| [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
Off-White | [Stability:]
Hygroscopic | [InChI]
InChI=1S/C23H27NP.2BrH/c1-24(2)19-12-20-25(21-13-6-3-7-14-21,22-15-8-4-9-16-22)23-17-10-5-11-18-23;;/h3-11,13-18H,12,19-20H2,1-2H3;2*1H/q+1;;/p-1 | [InChIKey]
NEQVFHFOWYYPBS-UHFFFAOYSA-M | [SMILES]
[P+](C1C=CC=CC=1)(C1C=CC=CC=1)(C1C=CC=CC=1)CCCN(C)C.[Br-].Br | [CAS DataBase Reference]
27710-82-3(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [F ]
3-10 |
| Hazard Information | Back Directory | [Uses]
(3-(Dimethylamino)propyl)triphenylphosphonium bromide is used as a reactant for preparing chlorpheniramine analogs reverse chloroquine resistance in Plasmodium falciparum by inhibiting PfCRT. |
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