Lithium chloride - UltraBio™, Ultra pure, ≥99%(T) , CAS No.7447-41-8

CAS: 7447-41-8 Cat. No.: L433505 Fórmula: LiCl Peso molecular: 42.39 Número EC: 231-212-3
Disponible para pedir
CALIDAD & PUREZA UltraBio™ ? UltraBio™ — Aladdin's line for molecular-biology applications. Use for nuclease-free, high-consistency reagents across molecular workflows. Ultra pure ? Ultra-pure grade with very low impurity content across the board. Use for trace analysis, electronics, or processes intolerant of contamination. ≥99%(T)
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
Room temperature,Argon charged,Desiccated
Shipped In
Normal
★
Talla
USA
Alemania (EU)*
Precio
Cantidad
25g
L433505-25g
Fabricado bajo pedido · 8–12 semanas
79,90US$
100g
L433505-100g
Fabricado bajo pedido · 8–12 semanas
259,90US$
Enter a quantity for the sizes you want to add.
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Por qué esta calidad

UltraBio™, Ultra pure, ≥99%(T) Ultra pure,UltraBio™ para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.

🌡

Almacenamiento y envío

Room temperature,Argon charged,Desiccated 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
UltraBio™, Ultra pure, ≥99%(T)
Condiciones de almacenamiento de almacenamiento
Room temperature,Argon charged,Desiccated
Enviado en
Normal
Grado
Ultra pure, UltraBio™
Pureza
≥99%(T)
Nombres e identificadores
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)

Datos de calidad específicos del lote. Introduzca su número de lote para obtener el COA exacto.

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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:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeFechaArticulo
F2623231F2623231Certificate of AnalysisMay 07, 2026 L433505
F2623262F2623262Certificate of AnalysisMay 07, 2026 L433505
Propiedades químicas y físicas
SolubilidadH2O: 1M, clear, colorless
SensibilidadMoisture 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
UltraBio™: Defining Excellence in Molecular Biology Applications
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
Reseñas

Reseñas de cliente

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