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Merck

R3375

Retinyl palmitate

Type IV, ~1,800,000 USP units/g, oil

Sinónimos:

Vitamin A palmitate, all−trans−Retinol palmitate

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Fórmula empírica (notación de Hill):
C36H60O2
Número CAS:
Peso molecular:
524.86
UNSPSC Code:
12352205
NACRES:
NA.79
PubChem Substance ID:
EC Number:
201-228-5
Beilstein/REAXYS Number:
1917366
MDL number:

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Nombre del producto

Retinyl palmitate, Type IV, ~1,800,000 USP units/g, oil

InChI key

VYGQUTWHTHXGQB-FFHKNEKCSA-N

InChI

1S/C36H60O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-25-35(37)38-30-28-32(3)23-20-22-31(2)26-27-34-33(4)24-21-29-36(34,5)6/h20,22-23,26-28H,7-19,21,24-25,29-30H2,1-6H3/b23-20+,27-26+,31-22+,32-28+

SMILES string

CC1=C(/C=C/C(C)=C/C=C/C(C)=C/COC(CCCCCCCCCCCCCCC)=O)C(C)(C)CCC1

biological source

synthetic (organic)

type

Type IV

assay

≥90% (HPLC)

form

oil

specific activity

~1,800,000 USP units/g

color

yellow to orange

mp

26 °C

storage temp.

2-8°C

Quality Level

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Este artículo
R15121602502PHR1235
assay

≥90% (HPLC)

assay

-

assay

-

assay

-

biological source

synthetic (organic)

biological source

synthetic (organic)

biological source

-

biological source

-

form

oil

form

solid or viscous liquid

form

-

form

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

mp

26 °C

mp

26 °C

mp

-

mp

-

color

yellow to orange

color

yellow to yellow-green

color

-

color

-

Application

Retinyl palmitate has been used as:
  • a retinoid derivative to modulate expression of connexin Cx26 and Cx30 in the cochlea[1]
  • a standard in high performance liquid chromatography(HPLC)
  • as a retinoid substrate in the isomerase assay of eyecup protein homogenates[2]

Biochem/physiol Actions

Retinoids are ligands to nuclear receptors and have antioxidant functionality.[3] Retinyl palmitate is widely used in pharmaceutical and cosmetic applications.[4] In sunscreen, it protects from UVB-induced DNA damage and apoptosis.[5] Retinyl palmitate is used to treat photoaging in skincare cosmetics.[4] Retinyl palmitate is an effective chemopreventive agent to treat lung cancer.[6] It also regulates various biological processes including cell differentiation and proliferation.[4]
Review: Vitamin A metabolism.

General description

Retinal, retinol and retinoic acid are the aldehyde, alcohol and acid forms of vitamin A, respectively.[4] The retinoids comprise a cyclohexenyl ring with a 20-carbon with double bonds in cis and trans configuration.[4] Retinyl palmitate is a major storage form of vitamin A. Retinyl esters provide pools of vitamin A that are converted into retinol and other retinoids as needed.[7] Retinoids also exist as retinyl esters such as retinyl propionate, retinyl acetate and retinyl palmitate.[4]

Packaging

Sealed ampule.

Physical form

Oil at room temperature

pictograms

Health hazard

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Repr. 1B

Clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Visite la Librería de documentos

Vitamin A or E and a catechin synergize as vaccine adjuvant to enhance immune responses in mice by induction of early interleukin-15 but not interleukin-1beta responses
Patel S, et al.
Immunology, 148(4), 352-362 (2016)
Effects of retinoid treatment on cochlear development, connexin expression and hearing thresholds in mice
Kim Y and Lin X
Journal of Otorhinolaryngology, Hearing and Balance Medicine settings, 1(1), 2-2 (2018)
Laboratory evaluation during high-dose vitamin A administration: a randomized study on lung cancer patients after surgical resection
Infante M, et al.
Journal of Cancer Research and Clinical Oncology, 117(2), 156-162 (1991)
Retinoids in cosmeceuticals
Sorg O, et al.
Dermatologic Therapy, 19(5), 289-296 (2006)
Safety of retinyl palmitate in sunscreens: a critical analysis
Wang SQ, et al.
Journal of the American Academy of Dermatology, 63(5), 903-906 (2010)

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