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n-Hexane - anhydrous, ≥98% , CAS No.110-54-3

CAS: 110-54-3 Cat. No.: H140380 Formula: C6H14 Molecular Weight: 86.18 Beilstein Registry Number: 1730733 EC Number: 203-777-6
2580 Citations COA
n-Hexane - anhydrous, ≥98% CAS No(110-54-3) by Aladdin Scientific
AVAILABLE TO ORDER
GRADE & PURITY Anhydrous Grade ? Anhydrous grade — water removed and packaged dry for moisture-sensitive chemistry. Use in reactions where even trace water would interfere or quench. ≥98%
Synonyms
Hexane, Laboratory Reagent, >=95% | FT-0657006 | n-Hexane, ACS grade | DTXCID001917 | Heksan | N-HEXANE [MI] | n-Hexane 100 microg/mL in Methanol | Epitope ID:116866 | Hexane, JIS special grade, >=96.0% | AI3-24253 | HEXANE | Hexane, for HPLC, >=97.0% (GC
Storage
Room temperature
Shipped In
FedEx DG Service
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Size
USA
Germany (EU)*
Price
Qty
100ml
H140380-100ml
1 In stock
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$74.90

$105.90
Save $31.00 (29.27%)
500ml
H140380-500ml
2 In stock
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$165.90

$192.90
Save $27.00 (14.00%)
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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Documents & Articles Citations of This Product Solution Calculators Reviews
🧪
Why this grade

anhydrous, ≥98% Anhydrous Grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships FedEx DG Service 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 2580 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
Hexane, Laboratory Reagent, >=95% | FT-0657006 | n-Hexane, ACS grade | DTXCID001917 | Heksan | N-HEXANE [MI] | n-Hexane 100 microg/mL in Methanol | Epitope ID:116866 | Hexane, JIS special grade, >=96.0% | AI3-24253 | HEXANE | Hexane, for HPLC, >=97.0% (GC
Specifications & Purity
anhydrous, ≥98%
Storage
Room temperature
Shipped In
FedEx DG Service
Grade
Anhydrous Grade
Purity
≥98%
Names and Identifiers
Pubchem Sid508813812
Canonical SmilesCCCCCC
IUPAC Namehexane
InChIKeyVLKZOEOYAKHREP-UHFFFAOYSA-N
INCHI1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3
Isomeric SMILES CCCCCC
WGK Germany 2
RTECS MN9275000
UN Number 1208
Packing Group II
Molecular Weight 86.18
Beilstein 1730733
Reaxy-Rn 1730733
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1730733&ln=

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

KingdomOrganic compounds
SuperclassHydrocarbons
ClassSaturated hydrocarbons
SubclassAlkanes
Intermediate Tree Nodes Not available
Direct ParentAlkanes
Alternative Parents Not available
Molecular FrameworkAliphatic acyclic compounds
Substituents Acyclic alkane - Alkane - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alkanes. These are acyclic branched or unbranched hydrocarbons having the general formula CnH2n+2 , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms.
External Descriptors a small molecule
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Listeria monocytogenes (2626 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bursaphelenchus xylophilus (372 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

84 results found

Lot NumberCertificate TypeDateItem
E2621483Certificate of AnalysisApr 20, 2026 H140380
E2621426Certificate of AnalysisApr 20, 2026 H140380
E2621486Certificate of AnalysisApr 20, 2026 H140380
E2621484Certificate of AnalysisApr 20, 2026 H140380
E2621418Certificate of AnalysisApr 20, 2026 H140380
E2621439Certificate of AnalysisApr 20, 2026 H140380
E2621438Certificate of AnalysisApr 17, 2026 H140380
E2621424Certificate of AnalysisApr 17, 2026 H140380
E2621420Certificate of AnalysisApr 15, 2026 H140380
E2621429Certificate of AnalysisApr 15, 2026 H140380
E2621434Certificate of AnalysisApr 15, 2026 H140380
D2615472Certificate of AnalysisMar 09, 2026 H140380
D2615473Certificate of AnalysisMar 09, 2026 H140380
D2615474Certificate of AnalysisMar 09, 2026 H140380
C2612528Certificate of AnalysisFeb 03, 2026 H140380
C2612527Certificate of AnalysisFeb 03, 2026 H140380
C2612526Certificate of AnalysisFeb 03, 2026 H140380
C2612524Certificate of AnalysisJan 22, 2026 H140380
C2612525Certificate of AnalysisJan 22, 2026 H140380
L2512479Certificate of AnalysisNov 28, 2025 H140380
L2512473Certificate of AnalysisNov 28, 2025 H140380
L2504353Certificate of AnalysisNov 28, 2025 H140380
L2504354Certificate of AnalysisNov 28, 2025 H140380
I2509390Certificate of AnalysisSep 03, 2025 H140380
I2509396Certificate of AnalysisSep 03, 2025 H140380
I2509400Certificate of AnalysisSep 03, 2025 H140380
I2509404Certificate of AnalysisSep 03, 2025 H140380
L2502107Certificate of AnalysisSep 03, 2025 H140380
I2509399Certificate of AnalysisSep 03, 2025 H140380
I2509402Certificate of AnalysisSep 03, 2025 H140380
I2509407Certificate of AnalysisSep 03, 2025 H140380
I2509409Certificate of AnalysisSep 03, 2025 H140380
I2509408Certificate of AnalysisSep 03, 2025 H140380
B2519230Certificate of AnalysisJan 15, 2025 H140380
B2519231Certificate of AnalysisJan 15, 2025 H140380
B2519227Certificate of AnalysisJan 15, 2025 H140380
B2519228Certificate of AnalysisJan 15, 2025 H140380
B2519229Certificate of AnalysisJan 15, 2025 H140380
A2507364Certificate of AnalysisDec 26, 2024 H140380
A2507363Certificate of AnalysisDec 26, 2024 H140380
A2507365Certificate of AnalysisDec 26, 2024 H140380
A2507367Certificate of AnalysisDec 26, 2024 H140380
H2408577Certificate of AnalysisJul 29, 2024 H140380
K2321474Certificate of AnalysisNov 02, 2023 H140380
K2321478Certificate of AnalysisNov 02, 2023 H140380
K2321475Certificate of AnalysisNov 02, 2023 H140380
K2321476Certificate of AnalysisNov 02, 2023 H140380
J2312509Certificate of AnalysisSep 13, 2023 H140380
I2307497Certificate of AnalysisAug 17, 2023 H140380
I2307496Certificate of AnalysisAug 07, 2023 H140380
H2310293Certificate of AnalysisAug 04, 2023 H140380
H2310292Certificate of AnalysisAug 04, 2023 H140380
H2310295Certificate of AnalysisJul 21, 2023 H140380
H2310300Certificate of AnalysisJul 21, 2023 H140380
H2310288Certificate of AnalysisJul 21, 2023 H140380
G2318798Certificate of AnalysisJul 03, 2023 H140380
G2318792Certificate of AnalysisJul 03, 2023 H140380
F23131518Certificate of AnalysisJun 06, 2023 H140380
F23131662Certificate of AnalysisJun 06, 2023 H140380
F23131532Certificate of AnalysisJun 06, 2023 H140380
F23131534Certificate of AnalysisJun 06, 2023 H140380
F23131551Certificate of AnalysisJun 06, 2023 H140380
F23131424Certificate of AnalysisJun 06, 2023 H140380
E2317434Certificate of AnalysisMar 29, 2023 H140380
E2317439Certificate of AnalysisMar 29, 2023 H140380
E2317431Certificate of AnalysisMar 29, 2023 H140380
L2220256Certificate of AnalysisNov 30, 2022 H140380
L2220252Certificate of AnalysisNov 30, 2022 H140380
L2220169Certificate of AnalysisNov 30, 2022 H140380
L2220257Certificate of AnalysisNov 30, 2022 H140380
L2220246Certificate of AnalysisNov 30, 2022 H140380
L2220155Certificate of AnalysisNov 30, 2022 H140380
K2224589Certificate of AnalysisNov 04, 2022 H140380
K2224588Certificate of AnalysisNov 04, 2022 H140380
K2224587Certificate of AnalysisNov 04, 2022 H140380
G2209231Certificate of AnalysisJun 30, 2022 H140380
G2209226Certificate of AnalysisJun 30, 2022 H140380
G2209225Certificate of AnalysisJun 30, 2022 H140380
F2229272Certificate of AnalysisJun 15, 2022 H140380
F2229271Certificate of AnalysisJun 15, 2022 H140380
F2229197Certificate of AnalysisJun 15, 2022 H140380
C2201255Certificate of AnalysisMar 08, 2022 H140380
C2201253Certificate of AnalysisMar 08, 2022 H140380
C2201239Certificate of AnalysisMar 08, 2022 H140380
Chemical and Physical Properties
SolubilitySoluble in ethanol, ether, acetone and chloroform, insoluble in water.
Refractive Index1.375
Flash Point(°F)-8°F
Flash Point(°C)-22℃
Boil Point(°C)69°C
Melt Point(°C)-95°C(lit.)
Molecular Weight86.180 g/mol
XLogP33.900
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count3
Exact Mass86.1096 Da
Monoisotopic Mass86.1096 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count6
Formal Charge0
Complexity12.000
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 Count1
Documents & Articles
The Guide to Anhydrous Grade for Reagents
Categories: Reagent Specifications, Grading and Purity
Tags:
Anhydrous Grade
A New Esterification Method — Rapid Esterification Mediated by the Coupling Reagent NDTP
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
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Esterification Method
Distillation Grade Reagents: Definition, Quality Control and Representative Aladdin Products
Categories: Reagent Specifications, Grading and Purity
Tags:
Grade Distillation grade
Carotenoids: Structural Features, Dietary Sources and Research Applications – With an Aladdin Natural Pigments Product Selection Guide
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Carotenoids
Fatty Acids from Basics to Lab Practice: Structural Classification, Research Uses, and Selection Tips (with an Aladdin Representative Product Quick-Reference Table)
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Fatty acids Long-chain carbon compounds
Recent Advances in Methods for Measuring Starch-Related Indices in Plants and Their Application-Oriented Selection
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Spectrophotometry Starch Soluble starch Total starch Amylose Amylopectin Resistant starch Iodine blue value Colorimetric assay
Plant Omics Panorama: Workflow Frameworks and Multi-Omics Integration from Genomics to Transcriptomics, Proteomics, and Metabolomics
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Proteomics Plant omics Genomics Transcriptomics Metabolomics Multi-omics integration Phenomics Epigenomics
Revisiting Titanium Tetrachloride: New Advances in the Direct Amidation and Esterification of Carboxylic Acids
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Extraction Methods and Process Selection for Flavonoid Compounds
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
flavonoid compounds extraction methods solvent extraction ultrasound-assisted extraction microwave-assisted extraction enzyme-assisted extraction supercritical fluid extraction process optimization
Preparation Methods and Precautions for Silane Coupling Agent Primer Solutions
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Silane Coupling Agent Primer Solutions
Guide to Traditional Natural Varnish Resins: Transparency, Gloss, Film Formation, Aging, and Application Selection of Dammar, Mastic, and Copal
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Natural resin Coating Material
Synthesis Strategy of Pentafluorothio Group-Synthesis of SF₅Cl
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Fluorinated block Halogenation Reagents Pentafluorosulfide Fluorination Reagent Pentafluorosulfidation Reaction Photocatalytic Reaction Continuous Flow Synthesis Process
Comparison of Bilirubin Detection Methods: Application Selection of the Diazo Method, Vanadate Oxidation Method, Bilirubin Oxidase Method, and HPLC
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Bilirubin Detection HPLC method Total Bilirubin Direct Bilirubin Indirect Bilirubin Diazo Method Vanadate Oxidation Method Bilirubin Oxidase Method
In Vitro Exposure Simulation and Bioaccessibility Assessment of Particulate Chemicals from Consumer Products Using Simulated Lung Fluid
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Bioaccessibility Simulated Lung Fluid In Vitro Exposure Simulation Particulate Chemicals Consumer Product Safety Inhalation Exposure Risk Assessment Organic Pollutants
One-Pot Arylation of the Piperidine α-C–H Bond: From Directed Lithiation and Li→Zn Transmetalation to Negishi Coupling
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Piperidine Saturated nitrogen-containing heterocyclic ring
Discovery and Structural Optimization of the Noncovalent 3CL Protease Inhibitor S-217622
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
3C-like protease main protease
Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Mitsunobu Reaction BEHT Protonated Betaine Alcohol Activation Primary Amines Secondary Amines Bimolecular Nucleophilic Substitution Inversion Of Configuration Α-Chiral Amines
Solid Supports in Packed Gas Chromatography Columns: Definition, Mechanisms of Action, Classification, and Selection
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Gas Chromatography
Citations of This Product
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