Cyclohexylamine - Moligand™, ≥99%(GC) , CAS No.108-91-8

CAS: 108-91-8 Cat. No.: C105035 분자식: C6H13N 분자량: 99.18 Beilstein Registry Number: 12,5 EC 번호: 203-629-0
주문 가능
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. ≥99%(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
FedEx DG Service
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Size
USA
독일 (EU)*
Price
Qty
100ml
C105035-100ml
3 재고 있음
—
US$14.90
500ml
C105035-500ml
3 재고 있음
—
US$27.90
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥99%(GC) Moligand™ 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

동의어
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
사양 및 순도
Moligand™, ≥99%(GC)
보관 조건
Protected from light,Room temperature
배송
FedEx DG Service
등급
Moligand™
순수함
≥99%(GC)
이름과 식별자
Pubchem Sid
정식 스마일
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
이성체 SMILES
C1CCC(CC1)N
WGK 독일
1
UN 번호
2357
포장 그룹
II
분자량
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.

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
SuperclassOrganic nitrogen compounds
분류Organonitrogen 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
설명This 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 구조
상호 작용 화학 구조 모델





관련 대상(인간)
SLC22A1 Tchem Solute carrier family 22 member 1 (646 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
작용 메커니즘
인증서(CoA, COO, BSE/TSE 및 분석 차트)
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.

24 results found

Lot NumberCertificate Type날짜항목
K2218187Certificate of AnalysisSep 04, 2026 C105035
F2624138Certificate of AnalysisJul 09, 2026 C105035
A2218368Certificate of AnalysisOct 29, 2025 C105035
E2105028Certificate of AnalysisFeb 07, 2025 C105035
E2105029Certificate of AnalysisFeb 07, 2025 C105035
E2331384Certificate of AnalysisJun 06, 2023 C105035
E2331383Certificate of AnalysisJun 03, 2023 C105035
E2305263Certificate of AnalysisMay 13, 2023 C105035
E2305271Certificate of AnalysisMay 13, 2023 C105035
E2331387Certificate of AnalysisMay 08, 2023 C105035
J2610106Certificate of AnalysisMay 08, 2023 C105035
E2305248Certificate of AnalysisMay 08, 2023 C105035
D2318511Certificate of AnalysisApr 22, 2023 C105035
D2318495Certificate of AnalysisApr 22, 2023 C105035
K2218169Certificate of AnalysisNov 21, 2022 C105035
K2210262Certificate of AnalysisNov 15, 2022 C105035
I2221259Certificate of AnalysisSep 27, 2022 C105035
I2221260Certificate of AnalysisSep 27, 2022 C105035
I2221261Certificate of AnalysisSep 27, 2022 C105035
I2212512Certificate of AnalysisSep 17, 2022 C105035
I2212513Certificate of AnalysisSep 17, 2022 C105035
I2212514Certificate of AnalysisSep 16, 2022 C105035
A2218364Certificate of AnalysisJan 24, 2022 C105035
A2218365Certificate of AnalysisJan 20, 2022 C105035
화학 및 물리적 특성
용해성Soluble in water and miscible with most organic solvents.
감도Light sensitive.
굴절률1.46
발화점(°C)27 °C
끓는점(°C)134°C
녹는점(°C)18 °C
분자량99.170 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
자주 묻는 질문과 기사
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
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