20211-76-1

Usage

Uses

Used in Fluid Catalytic Cracking (FCC) Catalysts:
Lanthanum Chloride Hydrate is used as a crucial raw material in the production of FCC catalysts, particularly for the manufacturing of high-octane gasoline from heavy crude oil. Lanthanum-rich Lanthanide compounds play a vital role in cracking reactions within the FCC process.
Used in Water Treatment:
Lanthanum Chloride Hydrate finds application in the water treatment industry, where it is employed for the precipitation of phosphate from solutions, thus aiding in the removal of harmful contaminants.
Used in Biochemical Research:
In the field of biochemical research, Lanthanum(III) chloride hydrate is utilized to block the activity of divalent cation channels, predominantly Calcium channels. This property makes it a valuable tool for studying the function and regulation of these channels in various biological systems.
Used as a Scintillator Material:
When doped with Cerium, Lanthanum Chloride Hydrate is used as a scintillator material in various applications, such as in gamma detectors, due to its ability to emit light upon interaction with ionizing radiation.
Used in the Synthesis of Aqueous Sol-Gel Lanthanum Phosphate Nanorods:
Lanthanum(III) chloride serves as a precursor for the synthesis of aqueous sol-gel lanthanum phosphate nanorods, which have potential applications in various fields, including catalysis and energy storage.
Used as a Filter Aid and Flocculent:
Lanthanum(III) chloride is also used as an effective flocculent and filter aid in industrial processes, enhancing the separation and purification of various substances.
Used as a Catalyst in Organic Synthesis:
Acting as a Lewis acid catalyst, Lanthanum(III) chloride is employed in the high-pressure oxidative chlorination of methane to chloromethane and other organic synthesis reactions, contributing to the production of valuable chemicals and materials.

InChI:InChI=1/3ClH.La.H2O/h3*1H;;1H2/q;;;+3;/p-3

Upstream product

• 7647-01-0 hydrogenchloride 
• 7732-18-5 water 
• 10025-84-0 LaCl₃*3H₂O 
• 10025-84-0 lanthanum(III) chloride heptahydrate 
• 10025-84-0 lanthanum(III) chloride hexahydrate 

Downstream Products

• 1215781-47-7 La₂(o-methylbenzoate)6(1,10-phenanthroline)2*H₂O 

Relevant academic research and scientific papers

Solubility in the LaCl3-LnCl3-HCl-H2O (Ln = Pr, Nd) systems at 25°C

The solubility in the quaternary water-salt systems LaCl 3-NdCl3-HCl-H2O (1) and LaCl3- PrCl3-HCl-H2O (2) at 25°C was studied in the section of 40 wt % hydrochloric acid, a system with a eutonic discontinuity. The composition at the point of discontinuity for the eutonic solution is the following. In system 1: 4.67 wt % LaCl3 · 7H2O, 0.37 wt % PrCl3 · 7H2O, 37.98 wt % HCl, and 56.98 wt % H2O; in system 2: 4.37 wt % LaCl3 · 7H 2O, 0.93 wt % NdCl3 · 6H2O, 37.88 wt % HCl, and 56.82 wt % H2O.

Facile solid-state chemical synthesis of novel ternary lanthanide complexes at room temperature

This paper reports a facile one-step synthesis of two ternary lanthanide complexes via room temperature solid-state reactions of lanthanide chloride hydrates with two ligands, potassium sorbate (PS), and 8-hydroxyquinoline (8-hq). The structural features, composition, and the morphologies of two complexes are characterized by elemental analysis, UV-Vis, FT-IR, XRD, SEM, and EDX. The thermal property of two ternary lanthanide complexes was also investigated. UV-Vis and FT-IR results confirm the coordination of lanthanide ion with two ligands. XRD results show that signals of complexes are not from reactants, and are believed to originate from the corresponding ternary lanthanide complex.

Synthesis, structure, thermal and luminescent behaviors of lanthanide-Pyridine-3,5-dicarboxylate frameworks series

The isostructural series of lanthanide pyridine-3,5-dicarboxylates of the formula [Ln2pdc3(dmf)2]·(dmf) x(H2O)y where Ln are lanthanides from La(III) to Lu(III); pdc2--C5/s

Dehydration and oxidation in the preparation of Ce-doped LaCl3 scintillation crystals

Ce3+ activated LaCl3 is a promising scintillation crystal for radiation detection. The starting raw materials used to grow LaCl3 crystals are rather hygroscopic and XRD proves that LaCl3·7H2O and LaCl

Synthesis, structure, and antibacterial properties of ternary rare-earth complexes with o-methylbenzoic Acid and 1,10-phenanthroline1

Ternary rare-earth complexes with o-methylbenzoic acid (o-MBA) and 1,10-phenanthroline (Phen) Ln2(o-MBA)6(Phen)2 ? nH2O(n = 0, 1) (Ln = La, Pr, Y, Yb) were synthesized and characterized by elemental analysis, IR

Thermochemical properties of the rare earth complexes with pyromellitic acid

Fourteen rare earth complexes with pyromellitic acid were synthesized and characterized by means of chemical and elemental analysis, and TG-DTG. The constant-volume combustion energies of complexes, ΔcU, were measured by a precise rotating-bomb

Poly[[tetra-aqua-tris(μ3-2,2-dimethyl-malonato) dilanthanum(III)] mono-hydrate]

In the title complex, {[La2(C5H6O4)3(H2O)4]·H2O} n , the La atoms are connected by bridging O atoms from carboxyl-ate groups to build, through centres of inversion, two-dimensional layers parallel to the ac plane containing deca-nuclear 20-membered rings.

Synthesis, crystal structures, and luminescent properties of two types of lanthanide phosphonates

Hydrothermal reactions of different lanthanide(III) salts with an amino-diphosphonate ligand (H4L= C6H5CH 2N(CH2PO3H2)2) led to two series of lanthanide phosphonates, namely, Ln(H2L)(H3L) (Ln = La, 1; Pr, 2; Nd, 3; Sm, 4; Eu, 5; Gd, 6; Tb, 7). Compounds 1-5 feature a one-dimensional (1D) chain structure in which dimers of two edge-sharing LnO8 polyhedra are interconnected by bridging phosphonate groups, such 1D arrays are further interlinked via strong hydrogen bonds between non-coordinated phosphonate oxygen atoms into a two-dimensional (2D) layer with the phenyl groups of the ligands orientated toward the interlayer space. Compounds 6 and 7 also show a different ID array in which the LnO6 octahedra are bridged by phosphonate groups via corner-sharing, such chains are also further interlinked by hydrogen bonds into a 2D supramolecular layer. Compounds 5 and 7 emit red and green light with a lifetime of 2.1 and 3.7ms, respectively.

Synthesis and structural characterization of new lanthanide coordination polymers with nitrilotriacetic acid

Reported herein are the hydrothermal synthesis and crystal structures of four lanthanide coordination polymers with nitrilotriacetic acid (H 3NTA) [Ln(NTA)(H2O)]n (Ln=La, 1; Pr, 2; Nd, 3; Eu, 4). Despite similar syntheses, compounds 1 to 4 show transformation in coordination mode of NTA and coordination number of Ln3+ duo to lanthanide contraction. The Ln(III) ions in 1 and 2 are nine-coordinated and connected through octadentate bridging ligands (NTA) to form a three-dimensional network. The Ln(III) ions in 3 and 4 are eight-coordinated and bridged by heptadentate bridging ligands (NTA) to form an extended two-dimensional layer structure, which further construct a three-dimensional supramolecular structure via coordination bond and three-centered hydrogen bonding between adjacent layers.

Hydrothermal synthesis and structural characterization of three novel lanthanide coordination polymers with fumarate and 1,10-phenanthroline

Three novel lanthanide complexes, [Ln2(fum)3(phen) 2(H2O)2]n (Ln=La, 1; Pr, 2. fum=fumarate dianion; phen=1,10-phenanthroline) and [Er2(fum) 3(phen)2]n