Online Database of Chemicals from Around the World

Decyl alcohol
[CAS 112-30-1]

List of Suppliers
Jinan Huifengda Chemical Co., Ltd. China
www.jnhfdchem.com
+86 (531) 8887-2378
+86 (531) 8869-1900
jnhfdchem@163.com
Chemical distributor since 2006
chemBlink Standard supplier since 2007
Chemceed Corportaion USA
www.chemceed.com
+1 (715) 726-2300
+1 (715) 726-2300
inquiry@chemceed.com
Chemical distributor
chemBlink Standard supplier since 2009
Hefei TNJ Chemical Industry Co., Ltd. China
www.tnjchem.com
+86 (551) 6541-8684
+86 (551) 6541-8697
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink Standard supplier since 2010
BOC Sciences USA
www.bocsci.com
+1 (631) 485-4226
+1 (631) 614-7828
info@bocsci.com
Chemical manufacturer
chemBlink Standard supplier since 2010
Hangzhou Leap Chem Co., Ltd. China
www.leapchem.com
+86 (571) 8771-1850
market19@leapchem.com
QQ Chat
Chemical manufacturer since 2006
chemBlink Standard supplier since 2015
Alfa Aesar. USA
www.alfa.com
+1 (978) 521-6300
+1 (978) 521-6350
info@alfa.com
Chemical manufacturer
Avonchem/Chromos Express Ltd. UK
www.avonchem.co.uk
+44 (1625) 434-300
+44 (1625) 869-777
info@avonchem.co.uk
Chemical manufacturer
ChemSampCo, Inc. USA
www.chemsampco.com
+1 (609) 656-2440
+1 (609) 656-2446
sales@chemsampco.com
Chemical manufacturer since 1960
Chemos GmbH & Co. KG Germany
www.chemos.de
+49 871-966346-0
+49 871-966346-13
chemos@chemos.de
Chemical distributor
ChemPur GmbH Germany
www.chempur.de
+49 (721) 933-840
+49 (721) 47-2001
info@chempur.de
Chemical manufacturer
Whyte Chemicals UK
www.whytechemicals.co.uk
+44 (20) 8346-5946
+44 (20) 8349-4589
sales@whytechemicals.co.uk
Chemical distributor
City Chemical LLC USA
www.citychemical.com
+1 (203) 932-2489
+1 (203) 937-8400
sales@citychemical.com
Chemical distributor
Molekula Ltd UK
www.molekula.com
+44 (1747) 831-066
+44 (1747) 831-199
info@molekula.com
Chemical manufacturer
Carbone Scientific Co., Ltd. UK
www.carbonesci.com
+44 (870) 486-8629
+44 (870) 288-7399
sales@carbonesci.com
Chemical distributor
Chiron AS Norway
www.chiron.no
+47 (73) 874-490
+47 (73) 874-499
chiron@chiron.no
Chemical manufacturer

Identification
ClassificationOrganic raw materials >> Alcohols, phenols, phenolic compounds and derivatives >> Acyclic alcohol
NameDecyl alcohol
Synonyms1-Decanol; Capric alcohol
Molecular StructureDecyl alcohol molecular structure (CAS 112-30-1)
Molecular FormulaC10H22O
Molecular Weight158.28
CAS Registry Number112-30-1
EC Number203-956-9
FEMA2365
SMILESCCCCCCCCCCO
Properties
Density0.8±0.1 g/cm3 Calc.*, 0.829 g/mL (Expl.)
Melting point5 - 7 °C (Expl.)
Boiling point227.8±3.0 °C 760 mmHg (Calc.)*, 231 °C (Expl.)
Flash point101.7±4.6 °C (Calc.)*, 81.7 °C (Expl.)
Solubilitywater: insoluble, alcohol, ether: soluble (Expl.)
Index of refraction1.435 (Calc.)*, 1.437 (Expl.)
*Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbolssymbol symbol   GHS07;GHS09 Warning  Details
Risk StatementsH315-H319-H411-H412  Details
Safety StatementsP264-P264+P265-P273-P280-P302+P352-P305+P351+P338-P321-P332+P317-P337+P317-P362+P364-P391-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Skin irritationSkin Irrit.2H315
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.4H332
Acute hazardous to the aquatic environmentAquatic Acute1H400
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.4H302
Specific target organ toxicity - single exposureSTOT SE3H336
Serious eye damageEye Dam.1H318
Flammable liquidsFlam. Liq.2H225
Acute toxicityAcute Tox.3H331
Aspiration hazardAsp. Tox.1H304
Reproductive toxicityRepr.2H361
Specific target organ toxicity - single exposureSTOT SE2H371
Transport InformationUN 3082
SDSAvailable
up chemBlink Chemical Story
Decyl alcohol, or 1-decanol, is a straight-chain ten-carbon primary alcohol. Its structure places one polar hydroxyl group at the end of a long hydrophobic hydrocarbon chain, giving it the amphiphilic character that underlies many of its uses. It occurs naturally in some plant-derived materials but is also manufactured industrially as part of the fatty-alcohol family. 1-Decanol is used as a chemical intermediate and in formulations for surfactants, lubricants, plasticizers, flavors, fragrances, and personal-care materials. The terminal hydroxyl group can be esterified, etherified, oxidized, or converted into other derivatives, while the C10 chain contributes hydrophobicity. It is therefore less a single-purpose chemical than a versatile starting point for molecules that need a medium-length alkyl group plus a reactive oxygen-containing end.

Exact chemical identity matters because free forms, salts, stereoisomers, hydrates, metabolites, intermediates, and finished products can carry different registry numbers even when their names are closely related. These distinctions affect molecular weight, physical properties, analytical standards, formulation, and interpretation of literature. A reliable chemical database therefore follows the exact substance instead of automatically transferring every property of a related form.

Functional groups are also a map of intended reactivity. Carbonyls, alcohols, amines, halides, alkenes, and heterocycles provide different opportunities for bond formation, while hydrocarbon frameworks influence shape and solubility. In multistep synthesis, the usefulness of an intermediate often comes from being able to transform one position selectively while leaving another group available for a later operation.

Modern chemical development depends as much on characterization as on synthesis. Identity, purity, stereochemistry, water or salt content, and process-related impurities may all need control. Well-characterized intermediates and reference materials therefore matter even when they never become a final commercial product: they make complex manufacturing and research reproducible.

A responsible Chemical Story distinguishes documented use from structural possibility. A familiar molecular scaffold can suggest a hypothesis, but resemblance alone does not establish a biological target, approved indication, or commercial application. When exact-CAS literature is limited, verified chemistry and clearly documented uses are more informative than speculation.

Seen broadly, practical performance emerges from the whole molecular system. Structure, stereochemistry, physical form, synthetic route, reaction environment, and, for biological molecules, metabolism can all determine what a substance actually does. Connecting these details to a documented historical, industrial, or biological role turns a registry entry into a meaningful chemical story.

Exact chemical identity matters because free forms, salts, stereoisomers, hydrates, metabolites, intermediates, and finished products can carry different registry numbers even when their names are closely related. These distinctions affect molecular weight, physical properties, analytical standards, formulation, and interpretation of literature. A reliable chemical database therefore follows the exact substance instead of automatically transferring every property of a related form.

Functional groups are also a map of intended reactivity. Carbonyls, alcohols, amines, halides, alkenes, and heterocycles provide different opportunities for bond formation, while hydrocarbon frameworks influence shape and solubility. In multistep synthesis, the usefulness of an intermediate often comes from being able to transform one position selectively while leaving another group available for a later operation.

Modern chemical development depends as much on characterization as on synthesis. Identity, purity, stereochemistry, water or salt content, and process-related impurities may all need control. Well-characterized intermediates and reference materials therefore matter even when they never become a final commercial product: they make complex manufacturing and research reproducible.

References:
1. PubChem. 1-Decanol, CID 8174.
2. OECD/SIDS assessment information for 1-decanol and related long-chain alcohols.

Market Analysis Reports
Related Products
Decursinol  Decursinol ange...  21-Decyano-25-D...  Decyano-Saframy...  Decyclopentyl Z...  N-Decylacetamid...  Decyl acetate  Decyl 2-(acetyl...  Decyl 2-(acetyl...  N-Decyl Acrylam...  n-Decyl-9,9,10,...  Decyl alcohol, ...  Decylamine  Decylamine, ace...  1-Decylamine Hy...  1-Decylamine Hy...  2-n-Decylaminoe...  N-Decylaminoeth...  (Z)-4-[[2-[[2-(...  N3''-[2-(Decyla...