Substance

ID:328744

(Benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate

Names and Identifiers
Synonyms
BOPCastros reagent卡特缩合剂(Benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate苯并三氮唑-1-基氧基三(二甲氨基)磷鎓六氟磷酸盐BOP ReagentBOP 试剂
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
Registration numbers
CAS Number
MDL Number
EC Number
Beilstein Number
PubChem SID
Properties
Safety Information
RID/ADR
UN 1325 4.1/PG 2
GHS Pictograms
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS02
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
European Hazard Symbols
Irritant Irritant (Xi)
Explosive Explosive (E)
UN Number
1325
Packing Group
2
GHS Precautionary statements
P210-P261
MSDS Link
Storage Temperature
2-8°C
Hazard Class
4.1
Safety Statements
35
German water hazard class
3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Supplemental Hazard Statements
Risk of explosion if heated under confinement.
GHS Signal Word
Danger
Risk Statements
2-11-37/38-44
GHS Hazard statements
H228-H315-H335
Product Information
Empirical Formula (Hill Notation)
C12H22F6N6OP2
Purity
97%
Physical Property
Melting Point
>130 °C (dec.)(lit.)
Molecule Details
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
Molecular Spectra
No Data Available
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References
No Data Available
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