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(Benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate_Molecular_structure_CAS_56602-33-6)
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(Benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate

Catalog No. 226084 Name Sigma Aldrich
CAS Number 56602-33-6 Website http://www.sigmaaldrich.com
M. F. C12H22F6N6OP2 Telephone 1-800-521-8956
M. W. 442.2806212 Fax
Purity 97% Email
Storage Chembase ID: 94885

SYNONYMS

Title
苯并三氮唑-1-基氧基三(二甲氨基)磷鎓六氟磷酸盐
IUPAC name
(1H-1,2,3-benzotriazol-1-yloxy)tris(dimethylamino)phosphanium; hexafluoro-λ5-phosphanuide
IUPAC Traditional name
(1,2,3-benzotriazol-1-yloxy)tris(dimethylamino)phosphanium hexafluorophosphate
Synonyms
BOP Reagent
BOP
Castros reagent
BOP 试剂
卡特缩合剂

DATABASE IDS

CAS Number 56602-33-6
MDL Number MFCD00011948
PubChem SID 24853542
Beilstein Number 4287025
EC Number 260-279-1

PROPERTIES

Empirical Formula (Hill Notation) C12H22F6N6OP2
Purity 97%
Melting Point >130 °C (dec.)(lit.)
GHS Pictograms GHS02
GHS Pictograms GHS07
GHS Signal Word Danger
GHS Hazard statements H228-H315-H335
European Hazard Symbols Explosive Explosive (E)
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P210-P261
RID/ADR UN 1325 4.1/PG 2
Risk Statements 2-11-37/38-44
Safety Statements 35
Storage Temperature 2-8°C
Supplemental Hazard Statements Risk of explosion if heated under confinement.
Hazard Class 4.1
UN Number 1325
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Reagent for: Peptide coupling1 Synthesis of esters2 Esterification of carboxylic acids3,4 Plasmid CAN-encapsulating liposomes5 Synthesis of magnolamide for antioxidative activity6Catalyst for preparation of 9-acridinecaroboxamide derivative7
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reagent for: Peptide coupling1 Synthesis of esters2 Esterification of carboxylic acids3,4 Plasmid CAN-encapsulating liposomes5 Synthesis of magnolamide for antioxidative activity6Catalyst for preparation of 9-acridinecaroboxamide derivative7

REFERENCES