methyl stearate (Q27137527)

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chemical compound

n-Octadecanoic acid methyl ester
Metholene 2218
Kemester 9718
Methyl ester of octadecanoic acid
Stearic acid methyl ester
Kemester 4516
Octadecanoic acid, methyl ester
Methyl octadecanoate
N-Octadecanoic acid, methyl ester
Methyl N-octadecanoate
Octadecanoic acid,methyl ester
Kemester 9018
Methyl (Z)-9-octadecenoate
Stearic acid, methyl ester

Language	Label	Description	Also known as
English	methyl stearate	chemical compound	n-Octadecanoic acid methyl ester Metholene 2218 Kemester 9718 Methyl ester of octadecanoic acid Stearic acid methyl ester Kemester 4516 Octadecanoic acid, methyl ester Methyl octadecanoate N-Octadecanoic acid, methyl ester Methyl N-octadecanoate Octadecanoic acid,methyl ester Kemester 9018 Methyl (Z)-9-octadecenoate Stearic acid, methyl ester

Statements

type of chemical entity

0 references

biogenic acyclic ester

0 references

0 references

298.287±0 dalton

1 reference

language of work or name

Methyl octadecanoate (English)

7 October 2016

chemical formula

C₁₉H₃₈O₂

1 reference

language of work or name

Methyl octadecanoate (English)

19 November 2016

canonical SMILES

CCCCCCCCCCCCCCCCCC(=O)OC

1 reference

language of work or name

Methyl octadecanoate (English)

19 November 2016

40 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

Astragalus membranaceus

1 reference

Volatile Flavor Components of ASTRAGALI RADIX (Astragalus membranaceusBunge)

Typhonium flagelliforme

1 reference

The cytotoxicity and chemical constituents of the hexane fraction of Typhonium flagelliforme (Araceace).

1 reference

Volatile components of zinchoge flower (Daphne odora Thunb.).

Myrtus communis

1 reference

Gas chromatographic—mass spectrometric investigations of the volatile components of myrtle berries (Myrtus communis L.)

Lepidium meyenii

1 reference

The in vitro biological activity of Lepidium meyenii extracts.

Haminoea templadoi

1 reference

Identification of the New 10,15-Eicosadienoic Acid and Related Acids in the Opisthobranch Haminaea templadoi

Aplysina lacunosa

1 reference

Isolation and characterization of novel 2-hydroxy fatty acids from the phospholipids of the sponge Smenospongia aurea

Aplysina fistularis

1 reference

Isolation and characterization of novel 2-hydroxy fatty acids from the phospholipids of the sponge Smenospongia aurea

Casimiroa greggii

1 reference

Oil of Chapote Amarillo (Sargentia greggi): 2,5-Dimethoxyflavone in the Unsaponified Fraction

1 reference

The Scent of Lotus Flowers

Azadirachta indica

1 reference

Volatile fraction of neem oil as a spermicide

Polygala senega

1 reference

Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots

1 reference

Volatile components of clove essential oil (Eugenia caryophyllus SPRENG): Neutral fraction.

Artemisia annua

1 reference

Composition of the essential oil from the root of Artemisia annua

Clusia burchellii

1 reference

Polyisoprenylated benzophenones from Clusia floral resins

Clusia grandiflora

1 reference

Polyisoprenylated benzophenones from Clusia floral resins

Clusia hilariana

1 reference

Polyisoprenylated benzophenones from Clusia floral resins

Clusia lanceolata

1 reference

Polyisoprenylated benzophenones from Clusia floral resins

1 reference

Polyisoprenylated benzophenones from Clusia floral resins

Clusia spiritu-sanctensis

1 reference

Polyisoprenylated benzophenones from Clusia floral resins

Clusia weddelliana

1 reference

Polyisoprenylated benzophenones from Clusia floral resins

Mentha pulegium

1 reference

Influence of in vitro growth conditions in the production of defence compounds in Mentha pulegium L.

Adenophora triphylla

1 reference

Phenolic Glycosides from Roots of Adenophora tetraphylla Collected in Heilongjiang, China.

Bauhinia purpurea

1 reference

Chemical Constituents of Heartwood ofBauhinia purpurea

Begonia heracleifolia

1 reference

Phytochemical and biological investigation of Begonia heracleifolia

Cinnamomum kotoense

1 reference

Antitubercular constituents from the stem wood of Cinnamomum kotoense

Hedysarum polybotrys

1 reference

Studies on the constituents of Hedysarum polybotrys Hand.-Mazz.

European Corn Borer

1 reference

Identification of an oviposition-deterring pheromone in the eggs of the European corn borer

Paris polyphylla var. chinensis

1 reference

Studies on the Constituents ofParis Formosana HayataPart II

Stellaria media

1 reference

Lipid constituents from stellaria media

Andrographis paniculata

1 reference

Antimicrobial compounds from leaf extracts of Jatropha curcas, Psidium guajava, and Andrographis paniculata.

Acyrthosiphon pisum

1 reference

A peculiar fatty acid, (Z,Z)-9,12,17-octadecatrienoic acid, identified in the phospholipids of the pea aphid,Acyrthosiphon pisum (Harris) (homoptera: aphididae)

Bathynella natans

1 reference

Tetratriacontanonaenoic acid, first natural acid with nine double bonds isolated from a crustacean Bathynella natans

Botryococcus braunii

1 reference

The fatty acids of the alga Botryococcus braunii

Cinnamomum philippinense

1 reference

Chemical constituents from the leaves of Cinnamomum philippinense

Diospyros mollis

1 reference

Components of fruits of Diospyros mollis

Gynura japonica

1 reference

Cerebrosides from the Rhizomes ofGynura Japonica

Maerua oblongifolia

1 reference

A lupane triterpenoid from Maerua oblongifolia

Plumeria obtusa

1 reference

Chemical constituents of leaves and stem bark of Plumeria obtusa.

Pueraria montana var. lobata

2 references

Volatile flavor components of Puerariae radix (Pueraria lobata Ohwi).

Isoflavonoids and the other constituents in callus tissues of Pueraria lobata.

Swietenia macrophylla

1 reference

A new phragmalin-type limonoid and anti-inflammatory constituents from the fruits of Swietenia macrophylla

Vaccinium vitis-idaea

2 references

The Aroma of Cranberries. II. Vaccinium macrocarpon Ait.

The Aroma of Cranberries. I. Vaccinium vitis-idaea L..

Hellenia speciosa

1 reference

Benzoquinones from Costus speciosus seeds

Neolitsea daibuensis

1 reference

Secondary metabolites from the roots of Neolitsea daibuensis and their anti-inflammatory activity

Smenospongia aurea

1 reference

Isolation and characterization of novel 2-hydroxy fatty acids from the phospholipids of the sponge Smenospongia aurea

Bonagota salubricola

1 reference

Identification and synthesis of the sex pheromone of Phtheochroa cranaodes (Lepidoptera: Tortricidae)

Mangifera indica

1 reference

Volatile components from mango (Mangifera indica L.) cultivars

1 reference

Cuticular waxes from potato (Solanum tuberosum) leaves

Apium graveolens

1 reference

Phytochemical and biological characterization of Italian "sedano bianco di Sperlonga" Protected Geographical Indication celery ecotype: A multimethodological approach

Humulus lupulus

1 reference

Bioactive components of the hop strobilus: comparison of different extraction methods by capillary electrophoretic and chromatographic methods

Garcinia dulcis

1 reference

Volatile constituents of fruits of Garcinia dulcis Kurz. from Cuba

Nicotiana tabacum

1 reference

Toxicological evaluation of aerosols of a tobacco extract formulation and nicotine formulation in acute and short-term inhalation studies

Zingiber officinale

1 reference

Chemistry, antioxidant and antimicrobial investigations on essential oil and oleoresins of Zingiber officinale

Astragalus trimestris

1 reference

Volatile Flavor Components of ASTRAGALI RADIX (Astragalus membranaceusBunge)

Astragalus mongholicus

1 reference

Volatile Flavor Components of ASTRAGALI RADIX (Astragalus membranaceusBunge)

Etlingera philippinensis

1 reference

Chemical constituents from the leaves of Cinnamomum philippinense

Commons category

Methyl stearate

0 references

Identifiers

InChI=1S/C19H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h3-18H2,1-2H3

1 reference

language of work or name

Methyl octadecanoate (English)

19 November 2016

HPEUJPJOZXNMSJ-UHFFFAOYSA-N

2 references

language of work or name

Methyl octadecanoate (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

Global Substance Registration System

language of work or name

methyl stearate (English)

19 November 2016

HPEUJPJOZXNMSJ-UHFFFAOYSA-N

CAS Common Chemistry

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=112-61-8

1 reference

language of work or name

Methyl stearate (English)

19 November 2016

2 references

language of work or name

Methyl octadecanoate (English)

19 November 2016

matched by identifier from

HPEUJPJOZXNMSJ-UHFFFAOYSA-N

mapping relation type

2 references

language of work or name

Methyl stearate (English)

7 October 2016

matched by identifier from

International Chemical Identifier

InChI=1S/C19H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h3-18H2,1-2H3

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

HPEUJPJOZXNMSJ-UHFFFAOYSA-N

UniChem compound ID

1 reference

MassBank accession ID

MSBNK-Fac_Eng_Univ_Tokyo-JP002661

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP003341

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP006225

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MSBNK-Fac_Eng_Univ_Tokyo-JP006250

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MSBNK-Fac_Eng_Univ_Tokyo-JP007105

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MSBNK-Fac_Eng_Univ_Tokyo-JP007714

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splash10-00dr-9100000000-e33d3c888348ee4595da

0 references

splash10-0002-1091000000-a8ca040a24cfff37f7e8

0 references

splash10-00du-9120000000-8de4d0b66a666bceb8d7

0 references

splash10-059f-9000000000-7bd9ba6fa57c2802c608

0 references

splash10-05fu-9000000000-71ef3d29b74452696ed8

0 references

splash10-001i-0090000000-8195d392b620d10c645d

0 references

splash10-001i-0090000000-804ba6de8c20d2188541

0 references

splash10-000i-9400000000-c995390ea83b8014e944

0 references

splash10-000i-9410000000-1df88d06542f79b504a3

0 references

NMRShiftDB structure ID

1 reference

matched by identifier from

HPEUJPJOZXNMSJ-UHFFFAOYSA-N

CAMEO Chemicals ID

0 references

0 references

1 reference

Hazardous Substances Data Bank

publication date

28 October 2019

METHYL STEARATE (English)

10 May 2021

DSSTox substance ID

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

matched by identifier from

HPEUJPJOZXNMSJ-UHFFFAOYSA-N

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

language of work or name

methyl stearate (English)

19 November 2016

ECHA Substance Infocard ID

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Methyl stearate (English)

CAS no.: 112-61-8 (English)

09.651

1 reference

CAS no.: 112-61-8 (English)

23 January 2021

09.651

1 reference

CosIng database

28 December 2019

METHYL STEARATE (English)

CAS no.: 112-61-8 (English)

Cannabis Database ID

1 reference

Cannabis Database

1 reference

Global Substance Registration System

language of work or name

methyl stearate (English)

19 November 2016

Human Metabolome Database ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

HPEUJPJOZXNMSJ-UHFFFAOYSA-N

3 references

language of work or name

Methyl stearate (English)

7 October 2016

based on heuristic

inferred from InChIKey

matched by identifier from

HPEUJPJOZXNMSJ-UHFFFAOYSA-N

2 references

Global Substance Registration System

language of work or name

methyl stearate (English)

19 November 2016

matched by identifier from

HPEUJPJOZXNMSJ-UHFFFAOYSA-N

Probes And Drugs ID

0 references

1 reference

https://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

30 June 2018

IEDB Epitope ID

1 reference

Immune Epitope Database and Analysis Resource

IEDB Epitope ID

19 May 2022

Google Knowledge Graph ID

0 references

Sitelinks

Wikipedia(2 entries)

dewiki Stearinsäuremethylester
zhwiki 硬脂酸甲酯

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)

commonswiki Category:Methyl stearate

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