n-Octanol - Moligand™, HPLC grade, ≥99.5% , CAS No.111-87-5

CAS: 111-87-5 Cat. No.: O119018 Formula: C8H18O Molecular Weight: 130.23 EC Number: 203-917-6
AVAILABLE TO ORDER
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. HPLC grade ? HPLC grade — purity and low UV-absorbing impurities suited to liquid chromatography. Use as the everyday solvent/reagent for routine HPLC. ≥99.5%
Synonyms
AI3-02169 | O0212 | OCTYL ALCOHOL [FCC] | Alcohol C8 | Alcohol C-8 | Dytol M-83 | Heptyl carbinol | 1-OCTANOL [FHFI] | 1-Octanol, puriss., >=99.5% (GC) | C00756 | N-octyl-alcohol | 1-octanol | 1-Octanol, SAJ first grade, >=75.0% | DTXCID101940 | KALCOHL-0
Storage
Room temperature
Shipped In
Normal
★
Size
Germany (EU)
USA*
Price
Qty
100ml
O119018-100ml
—
5 In stock
€12.93
500ml
O119018-500ml
3 In stock
4 In stock
€51.11
Enter a quantity for the sizes you want to add.
🧪
Why this grade

Moligand™, HPLC grade, ≥99.5% HPLC grade,Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature 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 275 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

1-Octanol is a synthetic reagent used to produce esters. 1-Octanol also inhibits T-type calcium channels and is used to determine the partition coefficient between compounds and the cytosol.
A T-type calcium channel blocker

Specifications

Synonyms
AI3-02169 | O0212 | OCTYL ALCOHOL [FCC] | Alcohol C8 | Alcohol C-8 | Dytol M-83 | Heptyl carbinol | 1-OCTANOL [FHFI] | 1-Octanol, puriss., >=99.5% (GC) | C00756 | N-octyl-alcohol | 1-octanol | 1-Octanol, SAJ first grade, >=75.0% | DTXCID101940 | KALCOHL-0
Specifications & Purity
Moligand™, HPLC grade, ≥99.5%
Storage
Room temperature
Shipped In
Normal
Grade
HPLC grade, Moligand™
Purity
≥99.5%
Names and Identifiers
Canonical Smiles
CCCCCCCCO
IUPAC Name
octan-1-ol
InChIKey
KBPLFHHGFOOTCA-UHFFFAOYSA-N
INCHI
1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3
Isomeric SMILES
CCCCCCCCO
RTECS
RH6550000
Alternate CAS
220713-26-8,68603-15-6,111-87-5
NSC Number
9823
MeSH Entry Terms
1 Octanol;1-Octanol;Alcohol, n-Octyl;n Octanol;n Octyl Alcohol;n-Octanol;n-Octyl Alcohol
Molecular Weight
130.23
Reaxy-Rn
1697461
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1697461&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
SuperclassLipids and lipid-like molecules
ClassFatty Acyls
SubclassFatty alcohols
Intermediate Tree Nodes Not available
Direct ParentFatty alcohols
Alternative Parents Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Fatty alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
External Descriptors a small molecule
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
GJA10 Tdark Gap junction alpha-10 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJA8 Tbio Gap junction alpha-8 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJA4 Tbio Gap junction alpha-4 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJB6 Tbio Gap junction beta-6 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJB1 Tbio Gap junction beta-1 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJB3 Tbio Gap junction beta-3 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJD4 Tdark Gap junction delta-4 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJE1 Tdark Putative gap junction epsilon-1 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJB4 Tbio Gap junction beta-4 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJA1 Tbio Gap junction alpha-1 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJA5 Tbio Gap junction alpha-5 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJA9 Tbio Gap junction alpha-9 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJB7 Tbio Gap junction beta-7 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJB2 Tbio Gap junction beta-2 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJD3 Tbio Gap junction delta-3 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJB5 Tbio Gap junction beta-5 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJD2 Tbio Gap junction delta-2 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJA3 Tbio Gap junction alpha-3 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJC1 Tbio Gap junction gamma-1 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJC2 Tbio Gap junction gamma-2 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GJC3 Tbio Gap junction gamma-3 protein (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cutibacterium acnes (887 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zygosaccharomyces bailii (36 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lithobates pipiens (29 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bursaphelenchus xylophilus (372 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Colletotrichum gloeosporioides (560 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 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.

119 results found

Lot NumberCertificate TypeDateItem
I2602514Certificate of AnalysisSep 04, 2026 O119018
I2602520Certificate of AnalysisSep 04, 2026 O119018
I2602522Certificate of AnalysisSep 04, 2026 O119018
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G2627256Certificate of AnalysisJul 30, 2026 O119018
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C2605649Certificate of AnalysisMar 16, 2026 O119018
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B2429431Certificate of AnalysisMar 11, 2024 O119018
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G2310600Certificate of AnalysisJul 14, 2023 O119018
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C2325791Certificate of AnalysisApr 13, 2023 O119018
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J2218184Certificate of AnalysisOct 19, 2022 O119018
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G2218040Certificate of AnalysisJul 30, 2022 O119018
F2222482Certificate of AnalysisJun 24, 2022 O119018
C2223043Certificate of AnalysisAug 09, 2021 O119018
C2223070Certificate of AnalysisAug 09, 2021 O119018
H2219145Certificate of AnalysisAug 09, 2021 O119018
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Chemical and Physical Properties
SolubilityInsoluble in water; Degree of Solubility in water: 0.3 mg/l 20 °C; Miscible with Chloroform,Ether,Alcohol
x_refractive_index1.4295
x_flash_point_drop_fahrenheit181.4 °F
x_flash_point_drop_centigrade83℃
x_boil_point_char194.45°C
x_melt_point_char-16°C(lit.)
Molecular Weight130.229 g/mol
XLogP33.000
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count6
Exact Mass130.136 Da
Monoisotopic Mass130.136 Da
Topological Polar Surface Area20.200 Ų
Heavy Atom Count9
Formal Charge0
Complexity43.800
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
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