Lithium chloride - anhydrous, 99.99% metals basis , CAS No.7447-41-8

CAS: 7447-41-8 Cat. No.: L130112 Fórmula: LiCl Peso molecular: 42.39 Número EC: 231-212-3
Disponible para pedir
Synonyms
CCRIS 5924 | HSDB 4281 | Lithium chloride, puriss. p.a., ACS reagent, anhydrous, >=99.0% (AT) | NCGC00093980-01 | (2R)-2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-3-naphthalen-2-ylpropanoic acid | (S)-N-(9-FLUORENYLMETHOXYCARBONYL)-2-AMINO-4-PENTYNOIC ACI
Storage
Argon charged,Room temperature
Shipped In
Normal
★
Talla
Alemania (EU)
USA*
Precio
Cantidad
5g
L130112-5g
—
1 Disponible
61,52€
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Por qué esta calidad

anhydrous, 99.99% metals basis para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.

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Almacenamiento y envío

Argon charged,Room temperature Envío Normal. Consulte el COA específico del lote para conocer las especificaciones exactas.

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Documentos de calidad

SDS, COA, ficha técnica y hoja de especificaciones disponibles para descargar. COA específico del lote accesible mediante búsqueda por número de lote.

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Prueba documental

Citado en 1479 publicaciones revisadas por pares sobre cromatografía, síntesis orgánica y reacciones de acoplamiento cruzado.

Especificaciones

Sinónimos
CCRIS 5924 | HSDB 4281 | Lithium chloride, puriss. p.a., ACS reagent, anhydrous, >=99.0% (AT) | NCGC00093980-01 | (2R)-2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-3-naphthalen-2-ylpropanoic acid | (S)-N-(9-FLUORENYLMETHOXYCARBONYL)-2-AMINO-4-PENTYNOIC ACI
Especificaciones y pureza
anhydrous, 99.99% metals basis
Mecanismos bioquímicos y fisiológicos
Lithium Chloride is an antiviral metal halide utilized in a variety of assays to study cell-fate and neurobiology. In developing Xenopus embryos, lithium chloride is observed to exert inhibition of GSK-3β, yet not reported to be a general inhibitor of oth
Condiciones de almacenamiento de almacenamiento
Argon charged,Room temperature
Enviado en
Normal
Nombres e identificadores
Pubchem Sid
Sonrisas canónicas
[Li+].[Cl-]
IUPAC Name
lithium;chloride
InChIKey
KWGKDLIKAYFUFQ-UHFFFAOYSA-M
INCHI
1S/ClH.Li/h1H;/q;+1/p-1
Isómeros SMILES
[Li+].[Cl-]
WGK Alemania
3
RTECS
OJ5950000
Peso molecular
42.39

Documentación

📋 Hoja de datos de seguridad (SDS)

Documento completo sobre peligros, manipulación, almacenamiento y cumplimiento normativo.

<<<<<<< HEAD Descargar SDS → ======= Descargar SDS → >>>>>>> release248-p3

✅ Certificado de análisis (COA)

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📊 Ficha técnica

Resumen de referencia rápida de las especificaciones y aplicaciones del producto.

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🔬 Hoja de especificaciones

Atributos de calidad completos y criterios de aceptación para esta calidad.

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Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomInorganic compounds
SuperclassMixed metal/non-metal compounds
ClaseAlkali metal salts
SubclassAlkali metal chlorides
Intermediate Tree Nodes Not available
Direct ParentAlkali metal chlorides
Alternative Parents Inorganic lithium salts  Inorganic chloride salts  
Molecular FrameworkNot available
Substituents Alkali metal chloride - Inorganic lithium salt - Inorganic chloride salt - Inorganic salt
DescripciónThis compound belongs to the class of inorganic compounds known as alkali metal chlorides. These are inorganic compounds in which the largest halogen atom is Chlorine, and the heaviest metal atom is an alkali metal.
External Descriptors inorganic chloride - lithium salt
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSK3B Tclin Glycogen synthase kinase-3 beta (11785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ARSA Tbio Cerebroside-sulfatase (655 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSK3A Tclin Glycogen synthase kinase-3 alpha (3764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NB-4 (999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SH-SY5Y (11521 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FEN1 Tchem Flap endonuclease 1 (12055 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pfk 6-phospho-1-fructokinase (7870 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Impa1 Inositol monophosphatase 1 (16203 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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8 results found

Lot NumberCertificate TypeFechaArticulo
E2408449E2408449Certificate of AnalysisApr 23, 2024 L130112
E2408450E2408450Certificate of AnalysisApr 23, 2024 L130112
E2408451E2408451Certificate of AnalysisApr 23, 2024 L130112
I2312555I2312555Certificate of AnalysisSep 06, 2023 L130112
I2312556I2312556Certificate of AnalysisSep 06, 2023 L130112
C2321693C2321693Certificate of AnalysisApr 09, 2023 L130112
G2213367G2213367Certificate of AnalysisJul 04, 2022 L130112
G2213369G2213369Certificate of AnalysisJul 04, 2022 L130112
Propiedades químicas y físicas
SolubilidadSoluble in water (1 mg/ml), alcohol, ether, pyridine, nitrobenzene, acetone, and amyl alcohol.
SensibilidadHygroscopic;Moisture sensitive
Punto de ebullición (°C)1360℃
Punto de fusión (°C)605 °C (lit.)
Peso molecular42.400 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass41.9849 Da
Monoisotopic Mass41.9849 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count2
Formal Charge0
Complexity2.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Preguntas frecuentes y artículos
A Practical Guide to Organozinc Reagents for Synthesis (Organozinc Reagents): Structural Features, Key Reactions, and a Practical Selection Navigation (Including Aladdin Product Tables)
Selection of Common Research Salts: A Task Map for Alkali Metal Salts & Alkaline Earth Metal Salts (with Product Tables 1–6)
Perovskite PV/PeLED Precursor Guide: Selecting Metal Halide Salts, Key Conditions, and Reproducible Performance (including Product Tables 1–4 and a Selection Navigation Guide)
Plant Omics Panorama: Workflow Frameworks and Multi-Omics Integration from Genomics to Transcriptomics, Proteomics, and Metabolomics
Experimental Judgment in mRNA In Vitro Transcription: Template Design, 5′ Capping, and dsRNA Control
Establishment and Application of Animal Models of Epilepsy (EP)
Regioselective Deprotonative Metalation of Pyridines: C–H Acidity, Coordination Effects, and Metal Systems
Photoinduced Alkane C(sp³)–H Functionalization in the Absence of an Added Photocatalyst: Trace-Iron Effects
Citations of This Product
Calculadoras de soluciones
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