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  • 176302-73-1 Structure
  • Basic information

    1. Product Name: Strontium chloride-Sr82
    2. Synonyms: Strontium chloride-Sr82
    3. CAS NO:176302-73-1
    4. Molecular Formula: Cl2Sr
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 176302-73-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Strontium chloride-Sr82(CAS DataBase Reference)
    10. NIST Chemistry Reference: Strontium chloride-Sr82(176302-73-1)
    11. EPA Substance Registry System: Strontium chloride-Sr82(176302-73-1)
  • 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: 176302-73-1(Hazardous Substances Data)

176302-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176302-73-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,3,0 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 176302-73:
(8*1)+(7*7)+(6*6)+(5*3)+(4*0)+(3*2)+(2*7)+(1*3)=131
131 % 10 = 1
So 176302-73-1 is a valid CAS Registry Number.

176302-73-1Relevant articles and documents

Theoretical and Experimental Study of the Crystal Structures, Lattice Vibrations, and Band Structures of Monazite-Type PbCrO4, PbSeO4, SrCrO4, and SrSeO4

Errandonea, Daniel,Muoz, Alfonso,Rodrguez-Hernndez, Placida,Proctor, John E.,Sapia, Fernando,Bettinelli, Marco

, p. 7524 - 7535 (2015/08/11)

The crystal structures, lattice vibrations, and electronic band structures of PbCrO4, PbSeO4, SrCrO4, and SrSeO4 were studied by ab initio calculations, Raman spectroscopy, X-ray diffraction, and optical-absorpt

Novel alkali earth borohydride Sr(BH4)2 and borohydride-chloride Sr(BH4)Cl

Ravnsbaek,Nickels,Cerny,Olesen,David,Edwards,Filinchuk,Jensen

, p. 10877 - 10885 (2013/10/22)

Two novel alkali earth borohydrides, Sr(BH4)2 and Sr(BH4)Cl, have been synthesized and investigated by in-situ synchrotron radiation powder X-ray diffraction (SR-PXD) and Raman spectroscopy. Strontium borohydride, Sr(BH4)2, was synthesized via a metathesis reaction between LiBH4 and SrCl2 by two complementary methods, i.e., solvent-mediated and mechanochemical synthesis, while Sr(BH4)Cl was obtained from mechanochemical synthesis, i.e., ball milling. Sr(BH4)2 crystallizes in the orthorhombic crystal system, a = 6.97833(9) A, b = 8.39651(11) A, and c = 7.55931(10) A (V = 442.927(10) A3) at RT with space group symmetry Pbcn. The compound crystallizes in α-PbO2 structure type and is built from half-occupied brucite-like layers of slightly distorted [Sr(BH4)6] octahedra stacked in the a-axis direction. Strontium borohydride chloride, Sr(BH4)Cl, is a stoichiometric, ordered compound, which also crystallizes in the orthorhombic crystal system, a = 10.8873(8) A, b = 4.6035(3) A, and c = 7.4398(6) A (V = 372.91(3) A3) at RT, with space group symmetry Pnma and structure type Sr(OH)2. Sr(BH4)Cl dissociates into Sr(BH4)2 and SrCl2 at ~170 C, while Sr(BH4)2 is found to decompose in multiple steps between 270 and 465 C with formation of several decomposition products, e.g., SrB 6. Furthermore, partly characterized new compounds are also reported here, e.g., a solvate of Sr(BH4)2 and two Li-Sr-BH 4 compounds.

Synthesis and structural characterization of new phases in the cubic M 3Te2O6X2 (M = Sr, Ba; X = Cl, Br) structure family

Stoeger, Berthold,Weil, Matthias,Silich, Konstantin A.,Olenev, Andrey V.,Berdonosov, Peter S.,Dolgikh, Valery A.

, p. 1322 - 1329 (2011/11/05)

Four alkaline earth oxotellurate(IV) halides with common formula M 3Te2O6X2 (M = Sr, Ba; X = Cl, Br) have been prepared as polycrystalline powders and/or in the form of single crystals. All compounds crystallize in the cubic space group Fd (3) m with cell parameters a = 15.9351(4) A for Sr3Te2O 6Cl2 (single-crystal X-ray data), 16.052(5) A for Sr3Te2O6Br2 (powder X-ray data), 16.688(2) A for Ba3Te2O6Cl2 (single-crystal X-ray data) and 16.8072(3) A for Ba3Te 2O6Br1.64Cl0.36 (single-crystal X-ray data). The results of the crystal structure analyses reveal a rigid (3)[M3Te2O6]2+ framework which can be described as being composed of regular octahedra of two types of chemically non-bonded M6 octahedra that are capped by trigonal pyramidal [TeO3] anions located above every second face of one of the M 6 octahedra. The halide X- anions are situated in the voids of the [M3Te2O6]2+ framework. Dependent on the nature of the halogen, the anions show various kinds of occupational disorder which eventually led to a revision of the previous structure model of Ba3Te2O6Cl2. A comparative discussion with other structures of general formula M 3Ch2O6X2 (M = divalent metal; Ch = Te, Se; X = Cl, Br) is presented. Copyright

A group of new selenite-chlorides of strontium and d-metals (Co,Ni): Synthesis, thermal behavior and crystal chemistry

Berdonosov, Peter S.,Olenev, Andrey V.,Kuznetsov, Alexei N.,Dolgikh, Valery A.

, p. 77 - 82 (2009/04/14)

The new selenite-chlorides with composition Sr3(SeO3)2Cl2 (I) and Sr2M(SeO3)2Cl2 (M=Co, Ni (II and III)) were obtained. They crystallize in monoclinic system I: space

Strontium-copper selenite-chlorides: Synthesis and structural investigation

Berdonosov, Peter S.,Olenev, Andrei V.,Dolgikh, Valery A.

, p. 2368 - 2373 (2010/01/05)

Two new complex selenite-chlorides of strontium and copper Sr2Cu(SeO3)2Cl2 (I) and SrCu2(SeO3)2Cl2 (II) were obtained and characterized by X-ray diffraction technique,

Hydration of strontium chloride and rare-earth element oxychlorides

Basiev,Batyrev,Voronov,Konyushkin,Kuznetsov,Osiko,Samartsev,Samoilova,Fedorov

, p. 1035 - 1037 (2008/02/04)

Hydration and dehydration (on calcination) of SrCl2, YOCl, and HoOCl powders were studied.

On the chemical vapor transport of ternary transition metal- and earth

Steiner, Udo

, p. 1706 - 1714 (2008/10/09)

The chemical vapor transport of transition metal tungstates MWO4 (M=Mn, Co, Ni, Cu, Zn, Cd) was investigated in dependence on mean transport temperature (923 K to 1223 K) and amount of transport agent Cl2. All tungstates migrate in a temperature gradient ΕT = 100 K from the region of higher temperature to the lower temperature with migration rates of 0.5 to 8 mg/h depending on experimental conditions. The transport behaviour was determined by continuous measurement of mass change during the transport experiments. The results were compared to thermo chemical calculations and the influence of moisture content discussed in detail. MgWO4 migrates under the influence of Cl2 in a temperature gradient 1273 K to 1173 K (migration rate 0.7 mg/h), CaWO4 and SrWO4 in a temperature gradient 1423 K to 1323 K (migration rate 0.1 mg/h).

Ammonia Absorption on Alkaline Earth Halides as Ammonia Separation and Storage Procedure

Liu, Chun Yi,Aika, Ken-Ichi

, p. 123 - 131 (2007/10/03)

For the low pressure ammonia synthesis (~1 MPa, 573-623 K), 40-80 kPa of ammonia produced must be separated. For this purpose, the absorption behavior of five kinds of alkaline earth metal halides (MgCl2, CaCl2, CaBr2, SrC

Dentifrice-compatible silica particulates

-

, (2008/06/13)

Novel silica particulates especially adapted for formulation to dentifrice compositions exhibit unique physical and chemical properties. In one embodiment, silica particulates have a unique surface chemistry as to be at least 50% compatible with zinc values, and have a number of OH functions, expressed as OH/nm2, of at most 15 and a zero charge point (PZC) of from 3 to 6.5. In a second embodiment, particulates have a surface chemistry as to be at least 65%, and preferably at least 90% compatible with guanidine values, notably chlorhexidine, and acidity function thereof, Ho, of at least 3.3. In a third embodiment, silica particulates are compatible with organic amines, and have a pH, in aqueous suspension, which varies according to the equations pH≤7.5-0.7 log(C) and pH≥5.0-0.5 log(C) and which also varies as a function of the electrical conductivity thereof, according to the equations pH≤8.5-0.4 log(D) and pH≥7.0-0.6 log(D) wherein (C) represents the weight concentration of said silica suspension, expressed % SiO2 and (D) represents the electrical conductivity of such aqueous silica suspension expressed in microsiemens*cm-1. In a fourth embodiment, novel silica particulates are compatible with such metal cations as zinc, tin, strontium, and the like, as well as with the fluorides, and have a unique surface chemistry such that the number of OH- functions thereof, expressed in OH- /nm2, is equal to or less than 10, and also have a zero charge point (ZCP) ranging from 3 to 6.5 and a pH, in aqueous suspension, which varies as a function of the electrical conductivity thereof according to the equation pH=b-a log (D) in which a is a constant equal to or less than 0.6; b is a constant equal to or less than 8.5; and (D) represents the electrical conductivity of such aqueous silica suspension, expressed in microsiemens*cm-1

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