Thermo Scientific Chemicals

(3-Carboxypropyl)triphenylphosphonium bromide, 97%, Thermo Scientific Chemicals

Catalog number: A19302.14
25 g, Each
Thermo Scientific Chemicals

(3-Carboxypropyl)triphenylphosphonium bromide, 97%, Thermo Scientific Chemicals

Catalog number: A19302.14
25 g, Each
Quantity
Catalog number: A19302.14
also known as A19302-14
Price (EUR)
Quantity
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Chemical Identifiers

CAS
17857-14-6
IUPAC Name
(3-carboxypropyl)triphenylphosphanium bromide
Molecular Formula
C22H22BrO2P
InChI Key
NKVJKVMGJABKHV-UHFFFAOYSA-N
SMILES
[Br-].OC(=O)CCC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
Melting Point (clear melt)
243.0-252.0?C
Form
Powder
Appearance (Color)
White
Assay (Titration ex Bromide)
≥96.0 to ≤104.0%

Description

Reactant for preparation of Piperamide analogs as histone deacetylase (HDAC) inhibitors with antitumor activity, Boron-containing benzoxaboroles as antimalarial agents, Methyl alkenyl quinolones as antimycobacterial agents, Solandelactone E via Sharpless epoxidation, Taber cyclopropanation, chemoselective reductions and lithiation-borylation-allylation sequence, Organotin compounds as antifungal agents, Oleanolic acid derivatives as inhibitors of protein tyrosine phosphatase 1B for negative regulation of insulin pathway (a promising target for treatment of diabetes and obesity), 11-oxa prostaglandin analogs with ocular hypotensive activity.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Reactant for preparation of Piperamide analogs as histone deacetylase (HDAC) inhibitors with antitumor activity, Boron-containing benzoxaboroles as antimalarial agents, Methyl alkenyl quinolones as antimycobacterial agents, Solandelactone E via Sharpless epoxidation, Taber cyclopropanation, chemoselective reductions and lithiation-borylation-allylation sequence, Organotin compounds as antifungal agents, Oleanolic acid derivatives as inhibitors of protein tyrosine phosphatase 1B for negative regulation of insulin pathway (a promising target for treatment of diabetes and obesity), 11-oxa prostaglandin analogs with ocular hypotensive activity.

Solubility
Soluble in water. soluble in ethanol.

Notes
Hygroscopic. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, water, moisture.
RUO – Research Use Only

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    Safety and Handling


    Classification of the substance or mixture
    CLP classification - Regulation(EC) No 1272/2008
    Skin Corrosion/Irritation
    Category 2
    Serious Eye Damage/Eye Irritation
    Category 2
    Specific target organ toxicity - (single exposure)
    Category 3
    Label Elements
    Signal Word

    Warning

    Hazard Statements

    H315 - Causes skin irritation

    H319 - Causes serious eye irritation

    H335 - May cause respiratory irritation

    Precautionary Statements

    P280 - Wear protective gloves/protective clothing/eye protection/face protection

    P302 + P352 - IF ON SKIN: Wash with plenty of soap and water

    P304 + P340 - IF INHALED: Remove person to fresh air and keep comfortable for breathing

    P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing

    P312 - Call a POISON CENTER or doctor if you feel unwell