It is stable at common pressure and temperature, and it should be protected from oxides and water. Store under inert gas.

Structure, properties, spectra, suppliers and links for: BTPPC, 1100-88-5. It will need reagent NaOC(CH3)3 and solvent dioxane with the reaction time of 2 hours. Customer Service, Synonym: Call a POISON CENTER or doctor/physician if you feel unwell. Precautionary Statements: James McNulty; David McLeod. Insoluble in acetone. Benzylidene triphenylphosphoranes (formed with n-BuLi) are coupled by reaction with sulfur to give stilbenes, with elimination of triphenylphosphine sulfide: Chem. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing.

16. or 1-978-521-6350 Continue rinsing. National Technical Information Service.

1100-88-5 Revision Date California Prop.

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benzyltriphenylphosphonium chloride solubility

benzyltriphenylphosphonium chloride solubility

benzyltriphenylphosphonium chloride, to product, a percent yield of 50.7% was calculated.

Clear, Iodine, crystalline, 99.99+% (metals basis). InChI: InChI=1S/C25H22P.ClH/c1-5-13-22(14-6-1)21-26(23-15-7-2-8-16-23,24-17-9-3-10-18-24)25-19-11-4-12-20-25;/h1-20H,21H2;1H/q+1;/p-1 (3)Std. K9. May cause respiratory irritation. STBB0728K9 - enter the lot number STBB0728 without the filling-code Privacy Policy Questions?

This reaction will need solvent dimethylformamide with the reaction time of 3 hours.

Wear respiratory protection.

CAS: 1100-88-5 MDL: MFCD00011913 EINECS: 214-154-3 Synonyms: Benzyltriphenylphosphonium chloride Cl and molecular weight is 388.87.

• Is the solution warm to the touch at this point? 05427ES–021 - enter the lot number 05427ES without the filling-code

Reproduction of any materials from the site is strictly forbidden without permission. Cl Boiling Point: Molecular Weight: 388.87 Flash Point: 300°C Transport Information *Required Fields, [Hangzhou]86-571-87562588,87562561,87562573, Benzyltriphenylphosphonium tetrafluoroborate, Benzyltriphenylphosphonium, salt with isooctylphenol (1:1), 2-(Methylthio)pyrimidine-5-carboxylic acid, L-Leucinamide,N-acetyl-L-leucyl-N-[(1S)-1-formyl-3-(methylthio)propyl]-, Pyrazine,3,6-diethoxy-2,5-dihydro-2-(1-methylethyl)-, (2R)-, Quaternary ammonium compounds, alkylbenzyldimethyl, chlorides, BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX). email: ecommerce@alfa.com, Specialty/Bulk Sales

Molecular Weight 388.87 . Keep, Remove your current shopping cart and replace with the saved cart? • What color is the salt? Terms of Use, Keep your current shopping and add the saved Cart? IF ON SKIN: Wash with plenty of soap and water. Crosslinking agent for tube-like natural halloysite / fluorelastomer nanocompositesReactant for synthesis of: • Platinum chloro tetrazole complexes via azidation• Trans-stilbenes and cinnamates via Wittig olefination• Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment• Pentiptycenes for use as light-driven molecular brakesReactant for formation of archipelago structures for formation of petroleum asphaltenes. 8.

Fatal if swallowed. All Rights Reserved.

you enter 062K1064. Amine- and sulfonamide-promoted Wittig olefination reactions in water. Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others. 1978, 66 (1), 110-117.

Beilstein/REAXYS Number 3599868 . Sigma-Aldrich Products are sold exclusively through Sigma-Aldrich, Inc. The lab manual reports the melting point of trans-9-(2- phenylethenyl) anthracene as 1310 C. 2.)

If your I agree

Soluble in water and alcohol. Also used as phase-transfer catalysts in the synthesis of certain organic compounds.

Type in Product Names, Product Numbers, or CAS Numbers to see suggestions. P260 - P273 - P280 - P304 + P340 + P310 - P305 + P351 + P338 - P314. Benzyltriphenylphosphonium chloride can be used as a reactant for the synthesis of: • Platinum chloro-tetrazole complexes via azidation.• Trans-stilbenes and cinnamates via Wittig olefination.• Achiral N-hydroxyformamide inhibitors of ADAM-TS4 and ADAM-TS5 for osteoarthritis treatment.• Pentiptycenes for use as light-driven molecular brakes.• Archipelago structures for formation of petroleum asphaltenes.It is also used as a crosslinking agent for tube-like natural halloysite / fluorelastomer nanocomposites. Fatal if inhaled. Uses of Phosphonium,triphenyl(phenylmethyl)-, chloride (1:1): it can be used to produce 1-methoxy-4-trans-styryl-benzene at the temperature of 105 °C.

In many cases a COA can be faxed © 2020  Merck KGaA, Darmstadt, Germany and/or its affiliates. © Copyright 2020 Alfa Aesar, Thermo Fisher Scientific. It is used as a reactant for the synthesis of chemical compounds. Remove/Take off immediately all contaminated clothing. See also Appendix 1.

B32807 - Benzyltriphenylphosphonium chloride, Pricing & availability is not currently available. The yield is about 62%. In some cases, a COA may not be available on-line.

Tel: 1-800-343-7276 or 1-978-521-6405 Causes serious eye damage. Ber., 103, 2995 (1970). Site Use Terms 2011, 17 (32), 8794-8798. If you find a lot number such as TO09019TO - enter the lot Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. The yield is about 67%.

Interactions between large organic ions of opposite charge: VI.

Fax: 1-978-521-6366 InChIKey: USFRYJRPHFMVBZ-UHFFFAOYSA-M, Please post your buying leads,so that our qualified suppliers will soon G.I Mukhayer; S.S Davis. Keep, Replace your shopping cart with these items? Using the melting point apparatus, the melting point of the product synthesized in this laboratory experiment was found to be between 131 oc and 1340C.

P260-P264b-P270-P271-P280-P284-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P312-P330-P361-P363-P501c, Do not breathe dust/fume/gas/mist/vapours/spray. Use only outdoors or in a well-ventilated area.

Add 1 pipet of water, using this to try to rinse down any phophonium salt that’s stuck on the sides • Note: does the salt dissolve? Also used as phase-transfer catalysts in the synthesis of certain organic compounds. search was unable to find the COA you are looking for, you will be Benzyltriphenylphosphonium chloride is used as the accelerator of the Bisphenol AF curing system for fluoroelastomer.

You can disable the usage of cookies by changing the settings of your browser. Preparation: this chemical can be prepared by chloromethyl-benzene and triphenylphosphane by heating. OTS0555817. (M-F, 8AM-5PM EST) Wash contaminated clothing before reuse. Wear protective gloves/protective clothing/eye protection/face protection. Fax: 1-800-322-4757 When you are using this chemical, please be cautious about it as the following: This chemical is toxic in contact with skin and if swallowed. If you find a lot number with a filling-code such as 65 Components This product does not contain any chemicals known to State of California to cause cancer, birth defects, or any other reproductive harm.

(M-F, 8AM-7PM EST) 62K1064 – you will only find the COO if

Toxic in contact with skin. All Rights Reserved.

1100-88-5 Revision Date New Jersey Right To Know Components Benzyltriphenylphosphonium chloride CAS-No. Weigh out 0.480 g of benzyltriphenylphosphonium chloride 1 and place it into the test tube. Need larger quantities for your development, manufacturing or research applications?

  |   Rinse mouth.

Tel: 1-800-343-0660 or 1-978-521-6300 It is used as a reactant for the synthesis of chemical compounds.

Hazard Statements:

Wittig olefination with carbonyl compounds can be carried out under basic, 2-phase conditions; the phosphonium salt acts as its own phase-transfer catalyst: Synthesis, 295 (1973). Benzyltriphenylphosphonium chloride SDS Safety Data Sheet for Benzyltriphenylphosphonium chloride 821685. Journal of Colloid and Interface Science.

email: specialquotes@alfa.com, Technical Service BTPPC, Linear Formula C 6 H 5 CH 2 P(Cl)(C 6 H 5) 3.

It is irritating to eyes, respiratory system and skin and can cause burns. ... Solubility in mg/100g standard fat at 20°C provides substance information on the substance solubility in standard fat in milligram per 100 gram at a temperature of 20°C. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. (M-F, 8AM-5PM EST) When using it, you need wear suitable protective clothing, gloves and eye/face protection. If you find a lot number with a filling-code such as Benzyltriphenylphosphonium chloride CAS-No.

Hygroscopic. IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

presented with a COA Request form.

Insoluble in acetone. Wash face, hands and any exposed skin thoroughly after handling Do not eat, drink or smoke when using this product. ©2008 LookChem.com,License:ICP NO. following the words 'Lot' or 'Batch'. NSC 116712,

... Benzyltriphenylphosphonium chloride is used as the accelerator of the Bisphenol AF curing system for fluoroelastomer. More important for COO: enter a "0" if only two numbers are By browsing our website without changing the browser settings you grant us permission to store that information on your device. Lot and Batch Numbers can be found on a product's label

It is stable at common pressure and temperature, and it should be protected from oxides and water. Store under inert gas.

Structure, properties, spectra, suppliers and links for: BTPPC, 1100-88-5. It will need reagent NaOC(CH3)3 and solvent dioxane with the reaction time of 2 hours. Customer Service, Synonym: Call a POISON CENTER or doctor/physician if you feel unwell. Precautionary Statements: James McNulty; David McLeod. Insoluble in acetone. Benzylidene triphenylphosphoranes (formed with n-BuLi) are coupled by reaction with sulfur to give stilbenes, with elimination of triphenylphosphine sulfide: Chem. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing.

16. or 1-978-521-6350 Continue rinsing. National Technical Information Service.

1100-88-5 Revision Date California Prop.

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