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Merck
CN

R0271

13-cis-Retinol

synthetic, ≥90% (HPLC)

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About This Item

Empirical Formula (Hill Notation):
C20H30O
CAS Number:
Molecular Weight:
286.45
UNSPSC Code:
41116107
PubChem Substance ID:
MDL number:
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biological source

synthetic

assay

≥90% (HPLC)

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

shipped in

dry ice

storage temp.

−20°C

SMILES string

CC(=C/CO)\C=C\C=C(C)\C=C\C1=C(C)CCCC1(C)C

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Sealed ampule

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

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José Angel Campos-Sandoval et al.
Journal of medicinal chemistry, 54(13), 4378-4387 (2011-05-20)
Serum retinol binding protein (sRBP) is released from the liver as a complex with transthyretin (TTR), a process under the control of dietary retinol. Elevated levels of sRBP may be involved in inhibiting cellular responses to insulin and in generating
Laura H Riihimäki-Lampén et al.
Journal of medicinal chemistry, 53(1), 514-518 (2009-11-27)
The binding of therapeutically relevant synthetic retinoid derivatives to bovine and reindeer beta-lactoglobulin (betaLG) is demonstrated using fluorescence quenching and ultrafiltration/HPLC methods. Furthermore, synthesis of methyl (E)-3-[4-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)vinyl]phenyl]-acrylate 4 and (E)-3-[4-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)vinyl]phenyl]acrylic acid 5 is described. All studied compounds bind to both
George Magoulas et al.
European journal of medicinal chemistry, 44(6), 2689-2695 (2009-02-14)
Novel mono- and diacylated spermines, readily obtained using isolable succinimidyl active esters of acidic retinoids for the selective acylation of free spermine or in situ activated acidic retinoids for acylating selectively protected spermine followed by deprotection, were shown to inhibit
Hyojung Kim et al.
Bioorganic & medicinal chemistry, 16(12), 6387-6393 (2008-05-31)
A new hybrid, retinyl retinoate 1, was synthesized with a condensing reaction between retinol and retinoic acid to improve the photo-stability, and the in vitro biological activity of the hybrid was analyzed. This retinol derivative had enhanced thermal stability and
Xueliang Fang et al.
Journal of medicinal chemistry, 48(5), 1481-1488 (2005-03-04)
A comprehensive herbal medicine information system for cancer (CHMIS-C) has been developed. The current version of the database integrates information on more than 200 anticancer herbal recipes that have been used for the treatment of different types of cancer in

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