Skip to Content
Merck
CN

420107

Bromotris(dimethylamino)phosphonium hexafluorophosphate

98%

Synonym(s):

BroP, Bromotris(N-methylmethanaminato)-phosphorus hexafluorophosphate

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
BrP[N(CH3)2]3PF6
CAS Number:
50296-37-2
Molecular Weight:
388.07
UNSPSC Code:
12352101
PubChem Substance ID:
24866311
MDL number:
MFCD00191864

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Bromotris(dimethylamino)phosphonium hexafluorophosphate, 98%

InChI

1S/C6H18BrN3P.F6P/c1-8(2)11(7,9(3)4)10(5)6;1-7(2,3,4,5)6/h1-6H3;/q+1;-1

SMILES string

F[P-](F)(F)(F)(F)F.CN(C)[P+](Br)(N(C)C)N(C)C

InChI key

XELPBWPBGHCIKX-UHFFFAOYSA-N

assay

98%

reaction suitability

reaction type: Coupling Reactions

mp

>300 °C (lit.)

application(s)

peptide synthesis

Looking for similar products? Visit Product Comparison Guide

Application

Reagent for:
Conjugate addition of nitroalkanes to an acrylate equivalent
A novel polymer supported approach to nucleoside modification
Asymmetric hydrogenations
Peptide coupling
Pyrrolidine hydroxylation
Synthesis of cyclic PNA-based compound directed against HIV-1 TAR RNA

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

wgk

WGK 3

pictograms

Health hazardCorrosion
GHS08,GHS05

signalword

Danger

hcodes

H314,H350

Hazard Classifications

Carc. 1B - Skin Corr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
011821/4V
1452305V
1452305
011821/4
09810TC

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

V R Scott et al.
Antimicrobial agents and chemotherapy, 32(8), 1154-1157 (1988-08-01)
Jasplakinolide is a cyclodepsipeptide which represents a new class of antifungal agents with potent activity against Candida albicans. Jasplakinolide is fungicidal against C. albicans with both a MIC and a minimum lethal concentration of 25 micrograms/ml in a broth dilution
S C Posey et al.
The Journal of biological chemistry, 274(7), 4259-4265 (1999-02-06)
Participation of the actin cytoskeleton in the transduction of proliferative signals has been established through the use of compounds that disrupt the cytoskeleton. To address the possibility that actin also participates in the transduction of an apoptotic signal, we have
Zizhuo Su et al.
Journal of vascular research, 57(5), 254-260 (2020-06-12)
The exocytosis of cyclophilin A (CyPA) by a vesicular pathway in response to reactive oxygen species has been determined. However, other sources of extracellular CyPA remain obscure. The aim of this study was to determine the role of autophagy in
A M Senderowicz et al.
Journal of the National Cancer Institute, 87(1), 46-51 (1995-01-04)
Jasplakinolide, a cyclodepsipeptide produced by an Indo-Pacific sponge, Jaspis johnstoni, has been reported to inhibit the growth of breast cancer cells. The effects of jasplakinolide on the proliferation of three human immortalized prostate carcinoma cell lines (PC-3, LNCaP, and TSU-Pr1)
J A Rosado et al.
The Journal of biological chemistry, 275(11), 7527-7533 (2000-03-14)
The nature of the mechanism underlying store-mediated Ca(2+) entry has been investigated in human platelets through a combination of cytoskeletal modifications. Inhibition of actin polymerization by cytochalasin D or latrunculin A had a biphasic time-dependent effect on Ca(2+) entry, showing
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service