Cyclohexylamine - Moligand™, Standard for GC, ≥99.5%(GC) , CAS No.108-91-8

CAS: 108-91-8 Cat. No.: C105033 Formula: C6H13N Molecular Weight: 99.18 Beilstein Registry Number: 12,5 EC Number: 203-629-0
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GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. Standard for GC ? GC reference standard — characterized compound for calibrating GC methods. Use to build calibration curves and verify GC quantitation. ≥99.5%(GC)
Synonyms
Cyclohexanamine | CYCLOHEXYLAMINE [MI] | n-cyclohexylamine | BIDD:ER0290 | BP-21278 | 4-12-00-00008 (Beilstein Handbook Reference) | Cyclohexylamine, 99.5% | Cyclohexylamine, ReagentPlus(R), 99% | MFCD00001486 | C00571 | DTXCID203996 | InChI=1/C6H13N/c7-6
Storage
Protected from light,Room temperature
Shipped In
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Size
USA
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Price
Qty
5ml
C105033-5ml
4 In stock
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$13.90

$20.90
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Why this grade

Moligand™, Standard for GC, ≥99.5%(GC) Moligand™,Standard for GC for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Protected from light,Room temperature Ships FedEx DG Service Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 42 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
Cyclohexanamine | CYCLOHEXYLAMINE [MI] | n-cyclohexylamine | BIDD:ER0290 | BP-21278 | 4-12-00-00008 (Beilstein Handbook Reference) | Cyclohexylamine, 99.5% | Cyclohexylamine, ReagentPlus(R), 99% | MFCD00001486 | C00571 | DTXCID203996 | InChI=1/C6H13N/c7-6
Specifications & Purity
Moligand™, Standard for GC, ≥99.5%(GC)
Storage
Protected from light,Room temperature
Shipped In
FedEx DG Service
Grade
Moligand™, Standard for GC
Purity
≥99.5%(GC)
Names and Identifiers
Pubchem Sid
Canonical Smiles
C1CCC(CC1)N
IUPAC Name
cyclohexanamine
InChIKey
PAFZNILMFXTMIY-UHFFFAOYSA-N
INCHI
1S/C6H13N/c7-6-4-2-1-3-5-6/h6H,1-5,7H2
Isomeric SMILES
C1CCC(CC1)N
WGK Germany
1
UN Number
2357
Packing Group
II
Molecular Weight
99.18
Beilstein
12,5
Reaxy-Rn
471175
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=471175&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.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClassOrganonitrogen compounds
SubclassCyclohexylamines
Intermediate Tree Nodes Not available
Direct ParentCyclohexylamines
Alternative Parents Organopnictogen compounds  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents Cyclohexylamine - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Amine - Aliphatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as cyclohexylamines. These are organic compounds containing a cyclohexylamine moiety, which consist of a cyclohexane ring attached to an amine group.
External Descriptors a small molecule
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
SLC22A1 Tchem Solute carrier family 22 member 1 (646 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.

4 results found

Lot NumberCertificate TypeDateItem
E2105025Certificate of AnalysisJul 30, 2026 C105033
E2331382Certificate of AnalysisMar 04, 2025 C105033
I2221256Certificate of AnalysisJun 12, 2024 C105033
K1815041Certificate of AnalysisMar 13, 2024 C105033
Chemical and Physical Properties
SolubilitySoluble in water and miscible with most organic solvents.
SensitivityLight sensitive.
Refractive Index1.46
Flash Point(°C)27 °C
Boil Point(°C)134°C
Melt Point(°C)18 °C
Molecular Weight99.170 g/mol
XLogP31.500
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass99.1048 Da
Monoisotopic Mass99.1048 Da
Topological Polar Surface Area26.000 Ų
Heavy Atom Count7
Formal Charge0
Complexity46.100
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
Standard for GC: A Practical Guide
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
Experimental Considerations for the Use of ADMP in the Conversion of Primary Amines to Organic Azides: Substrate Nucleophilicity, Base Matching, and Medium Selection
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
Citations of This Product
Solution Calculators
Reviews

Customer Reviews

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