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Merck

M1556000

Methyl 12-hydroxystearate

European Pharmacopoeia (EP) Reference Standard

Sinónimos:

12-Hydroxystearic acid methyl ester, Methyl 12-hydroxyoctadecanoate

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About This Item

Fórmula empírica (notación de Hill):
C19H38O3
Número de CAS:
Peso molecular:
314.50
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

pharmaceutical primary standard

API family

methyl 12-hydroxystearate

manufacturer/tradename

EDQM

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

CCCCCCC(O)CCCCCCCCCCC(=O)OC

InChI

1S/C19H38O3/c1-3-4-5-12-15-18(20)16-13-10-8-6-7-9-11-14-17-19(21)22-2/h18,20H,3-17H2,1-2H3

InChI key

RVWOWEQKPMPWMQ-UHFFFAOYSA-N

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General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Methyl 12-hydroxystearate EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

Related product

Referencia del producto
Descripción
Precios

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Certificados de análisis (COA)

Lot/Batch Number

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Allergic contact dermatitis to methyl hydroxystearate in a rubber respirator.
Emma C Benton et al.
Contact dermatitis, 67(4), 238-239 (2012-09-11)
Hiroki Ebata et al.
Macromolecular bioscience, 8(1), 38-45 (2007-10-24)
Novel green and sustainable elastomers having both good biodegradability and chemical recyclability properties were designed and synthesized using potentially biobased materials and lipase as an environmentally benign catalyst. High molecular weight poly[(12-hydroxydodecanoate)-co-(12-hydroxystearate)] [poly(12HD-co-12HS)] samples with varying monomer ratios were prepared
M S Jie et al.
Lipids, 27(1), 59-64 (1992-01-01)
Methyl oleate (18:1) and linoleate (18:2) were readily transformed to the corresponding gem-dichlorocyclopropane derivatives in high yield, using triethylbenzylammonium chloride as the phase-transfer catalyst in the presence of aqueous NaOH and CHCl3. Reaction of dichlorocarbene with methyl 12-hydroxystearate furnished methyl

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