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About This Item
Empirical Formula (Hill Notation):
C19H38O3
CAS Number:
Molecular Weight:
314.50
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:
Product Name
Methyl 12-hydroxystearate, European Pharmacopoeia (EP) Reference Standard
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
SMILES string
CCCCCCC(O)CCCCCCCCCCC(=O)OC
InChI key
RVWOWEQKPMPWMQ-UHFFFAOYSA-N
grade
pharmaceutical primary standard
API family
methyl 12-hydroxystearate
manufacturer/tradename
EDQM
application(s)
pharmaceutical (small molecule)
format
neat
storage temp.
2-8°C
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Application
Methyl 12-hydroxystearate EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.
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.
Other Notes
Sales restrictions may apply.
Packaging
The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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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