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diphenylantimony diisopropyldithiophosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126443-52-5 Structure
  • Basic information

    1. Product Name: diphenylantimony diisopropyldithiophosphate
    2. Synonyms: diphenylantimony diisopropyldithiophosphate
    3. CAS NO:126443-52-5
    4. Molecular Formula: C18H24O2PS2Sb
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126443-52-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: diphenylantimony diisopropyldithiophosphate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diphenylantimony diisopropyldithiophosphate(126443-52-5)
    11. EPA Substance Registry System: diphenylantimony diisopropyldithiophosphate(126443-52-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 126443-52-5(Hazardous Substances Data)

126443-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126443-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,4 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126443-52:
(8*1)+(7*2)+(6*6)+(5*4)+(4*4)+(3*3)+(2*5)+(1*2)=115
115 % 10 = 5
So 126443-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H15O2PS2.2C6H5.Sb/c1-5(2)7-9(10,11)8-6(3)4;2*1-2-4-6-5-3-1;/h5-6H,1-4H3,(H,10,11);2*1-5H;/p-1/rC12H10Sb.C6H15O2PS2/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-5(2)7-9(10,11)8-6(3)4/h1-10H;5-6H,1-4H3,(H,10,11)/p-1

126443-52-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenylantimony,propan-2-yloxy-propan-2-ylsulfanyl-sulfanylidenephosphanium

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:126443-52-5 SDS

126443-52-5Downstream Products

126443-52-5Relevant articles and documents

Cleavage reactions of triphenylantimony with dialkyl (or alkylenyl) dithiophosphoric acids

Chaturvedi,Nagar,Rai

, p. 1025 - 1033 (2008/10/09)

Triphenylantimony reacts with dialkyl (or alkylenyl) dithiophosphoric acids in 1:1 and 1:2 molar ratio to form complexes of the types Ph3-n Sb[S2P(OR)2]n and Ph3-nSb[S2POGO]n (R

Phenylantimony(III) diorganophosphorodithioates: the crystal structure of diphenylantimony(III) di-isopropylphosphorodithioate, Ph2SbS2P(OiPr)2; unusual polymerisation through semibonding

Silvestru, Christian,Curtui, Maria,Haiduc, Ionel,Begley, Michael J.,Sowerby, D. Bryan

, p. 49 - 58 (2007/10/02)

The diphenylantimony(III) phosphorodithioates, Ph2SbS2P(OR)2 where R = Me, Et, iPr and Ph, have been prepared and the methyl and isopropyl derivatives obtained as crystalline solids.The compounds have been characterised by infrared and NMR spec

O,O-DIALKYL DITHIOPHOSPHATE COMPLEXES OF DIPHENYL ANTIMONY (III)

Karra, R.,Singh, Y. P.,Rai, A. K.

, p. 145 - 150 (2007/10/02)

Reactions of diphenylantimony chloride with the sodium salts of O,O-dialkyldithiophosphoric acids in 1:1 molar ratio in benzene solution yield neutral complexes with the general formula (RO)2PS2SbPh2 (where R = CH3, C2H5, n-C3H7, i-C3H7, n-C4H9, i-C4H9).These complexes are monomeric in nature and have been characterized by IR, 1H, 13C and 31P spectroscopy.The 31P nmr spectral data are consistent with the chelating behaviour of the dithiophosphate moieties. - Key words: O,O-dialkyldithiophosphates; Diphenyl antimony; Chelates; Monomers; Spectral Studies; Five-coordinated antimony.

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