Lithium bromide - PrimorTrace™, ≥99.99% metals basis, used for Lithium bromide (LiBr) can be used as a catalyst for the following studies: Convert (aromatic - and α, β - unsaturated) aldehydes into dithioacetals through solvent-free dithioacetal reaction.

CAS: 7550-35-8 Cat. No.: L108935 Formula: LiBr Molecular Weight: 86.85 EC Number: 231-439-8 PubChem CID: 82050
AVAILABLE TO ORDER
GRADE & PURITY PrimorTrace™ ? PrimorTrace™ — Aladdin's trace-metal-analysis line with ultra-low metal background. Use for ICP/AAS trace-metal work where contamination must be minimal. ≥99.99% metals basis
Synonyms
LITHIUM BROMATUM | Lithium monobromide | Lithium bromide (LiBr) | MFCD00011077 | 2Z3E1OF81V | D08135 | lithium;bromide | SMR000279821 | AMXOYNBUYSYVKV-UHFFFAOYSA-M | LITHIUM BROMIDE [WHO-DD] | MFCD00066850 | CCRIS 7361 | AKOS015832995 | bromolithium | LIT
Storage
Protected from light,Room temperature,Argon charged
Shipped In
Normal
★
Size
Germany (EU)
USA*
Price
Qty
5g
L108935-5g
—
2 In stock
€69.33
25g
L108935-25g
—
2 In stock
€203.83
100g
L108935-100g
—
1 In stock
€485.85
Enter a quantity for the sizes you want to add.
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Why this grade

PrimorTrace™, ≥99.99% metals basis PrimorTrace™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 401 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Extremely deliquescent, non-toxic, odorless, slightly bitter in taste, highly soluble in water and releases heat, soluble in organic solvents such as methanol, acetone, ethanol, ether, and ethylene glycol, and slightly soluble in pyridine Used as a water vapor absorbent, air humidity regulator, absorption refrigerant, etc.

Specifications

Synonyms
LITHIUM BROMATUM | Lithium monobromide | Lithium bromide (LiBr) | MFCD00011077 | 2Z3E1OF81V | D08135 | lithium;bromide | SMR000279821 | AMXOYNBUYSYVKV-UHFFFAOYSA-M | LITHIUM BROMIDE [WHO-DD] | MFCD00066850 | CCRIS 7361 | AKOS015832995 | bromolithium | LIT
Specifications & Purity
PrimorTrace™, ≥99.99% metals basis
Application
Lithium bromide (LiBr) can be used as a catalyst for the following studies: Convert (aromatic - and α, β - unsaturated) aldehydes into dithioacetals through solvent-free dithioacetal reaction. Synthesize olefins through the condensation reaction of carbon
Storage
Protected from light,Room temperature,Argon charged
Shipped In
Normal
Grade
PrimorTrace™
Purity
≥99.99% metals basis
Names and Identifiers
Pubchem Sid
Canonical Smiles
[Li+].[Br-]
IUPAC Name
lithium;bromide
InChIKey
AMXOYNBUYSYVKV-UHFFFAOYSA-M
INCHI
1S/BrH.Li/h1H;/q;+1/p-1
Isomeric SMILES
[Li+].[Br-]
WGK Germany
3
PubChem CID
82050
Molecular Weight
86.85

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomInorganic compounds
SuperclassMixed metal/non-metal compounds
ClassAlkali metal salts
SubclassAlkali metal bromides
Intermediate Tree Nodes Not available
Direct ParentAlkali metal bromides
Alternative Parents Inorganic lithium salts  
Molecular FrameworkNot available
Substituents Alkali metal bromide - Inorganic lithium salt - Inorganic salt
DescriptionThis compound belongs to the class of inorganic compounds known as alkali metal bromides. These are inorganic compounds in which the largest halogen atom is Bromine, and the heaviest metal atom an alkali metal.
External Descriptors lithium salt - bromide salt
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

13 results found

Lot NumberCertificate TypeDateItem
F2608389Certificate of AnalysisJun 10, 2026 L108935
F2608390Certificate of AnalysisJun 10, 2026 L108935
F2608391Certificate of AnalysisJun 10, 2026 L108935
F2506543Certificate of AnalysisJun 14, 2025 L108935
F2506544Certificate of AnalysisJun 14, 2025 L108935
F2506548Certificate of AnalysisJun 14, 2025 L108935
I2410126Certificate of AnalysisSep 12, 2024 L108935
I2410127Certificate of AnalysisSep 12, 2024 L108935
I2410128Certificate of AnalysisSep 12, 2024 L108935
E2417054Certificate of AnalysisMay 24, 2024 L108935
A2403082Certificate of AnalysisSep 21, 2023 L108935
L2116576Certificate of AnalysisSep 21, 2023 L108935
D2306057Certificate of AnalysisApr 11, 2023 L108935
Chemical and Physical Properties
SolubilitySoluble in water (at 20°C 1490g/L), alcohol and glycol.
SensitivityHygroscopic.Light sensitive.Moisture sensitive
x_boil_point_char1265°C
x_melt_point_char550℃
Molecular Weight86.900 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass85.9343 Da
Monoisotopic Mass85.9343 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
FAQs and Articles
Formaldehyde
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)
Experimental Judgment for Differential Deprotection of Double Boc and Related N-Boc Systems: Substrate Type, Site-Response Differences, and Initial Condition Selection
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
Construction and Transformation of Aziridines in Drug Synthesis: Ring Strain, N-Substituent Control, Selective Ring Opening, and Scaffold Expansion
Citations of This Product
Solution Calculators
Reviews

Customer Reviews

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