Pular para o conteúdo
Merck
Todas as fotos(1)

Documentos Principais

Visualizar Toda a Documentação

10810

Sigma-Aldrich

trans-β-Apo-8′-carotenal

≥96.0% (UV)

Sinônimo(s):

Apocarotenal

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(1)

About This Item

Fórmula empírica (Notação de Hill):
C30H40O
Número CAS:
1107-26-2
Peso molecular:
416.64
Beilstein:
2064131
Número CE:
214-171-6
Número MDL:
MFCD00042626
Código UNSPSC:
12352205
ID de substância PubChem:
57646819
NACRES:
NA.79

fonte biológica

synthetic

Ensaio

≥96.0% (UV)

Formulário

powder

perda

≤0.5% loss on drying, 20 °C (HV)

pf

137-141 °C

solubilidade

chloroform: 1 mg/mL, clear to very faintly turbid, intense red-orange

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

[H]C(=O)\C(C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(C)\C=C\C1=C(C)CCCC1(C)C

InChI

1S/C30H40O/c1-24(13-8-9-14-25(2)16-11-18-27(4)23-31)15-10-17-26(3)20-21-29-28(5)19-12-22-30(29,6)7/h8-11,13-18,20-21,23H,12,19,22H2,1-7H3/b9-8+,15-10+,16-11+,21-20+,24-13+,25-14+,26-17+,27-18+

chave InChI

DFMMVLFMMAQXHZ-DOKBYWHISA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Aplicação


  • Tackling the challenge of selective analytical clean-up of complex natural extracts: the curious case of chlorophyll removal: This study outlines a methodology for the selective analytical clean-up of complex natural extracts, which can be applied to enhance the purity and stability of trans-β-Apo-8′-carotenal, particularly useful in the context of life science manufacturing and research and development. This approach is crucial for maintaining the integrity of bioactive compounds during synthesis and storage (Bijttebier et al., 2014).

Ações bioquímicas/fisiológicas

Natural carotenoid that is formed from β-carotene in vivo and is an inducer of cytochrome P450 1A (CYP1A) in rats and in Ah-receptor-responsive mice.

Outras notas

Internal standard in the detection of citrus carotenoids by reversed-phase HPLC.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCG8064
BCCF6307
BCCF4598
BCCF4518
BCCC7705

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 5

1 of 5

β-Carotene synthetic, ≥95% (HPLC), crystalline

Sigma-Aldrich

C4582

β-Carotene

α-Carotene analytical standard

Supelco

50887

α-Carotene

Canthaxanthin ≥95.0% (HPLC)

Sigma-Aldrich

11775

Canthaxanthin

9-cis-Retinal vitamin A analog

Sigma-Aldrich

R5754

9-cis-Retinal

Cholesterol Esterase from Pseudomonas sp. lyophilized powder, ≥200,000 units/g protein

Sigma-Aldrich

C1403

Cholesterol Esterase from Pseudomonas sp.

Yuka Matsushita-Ishiodori et al.
Biochemical and biophysical research communications, 359(1), 157-162 (2007-05-29)
Mutations in human spastin (SPG4) cause an autosomal dominant form of hereditary spastic paraplegia. Sequence analysis revealed that spastin contains the AAA (ATPases associated with diverse cellular activities) domain in the C-terminal region. Recently, it was reported that spastin interacts
Feng Liu et al.
Proteomics, 6(9), 2673-2692 (2006-04-06)
Hematopoietic stem cells are capable of self-renewal and differentiation into different hematopoietic lineages. To gain a comprehensive understanding of hematopoietic stem/progenitor cells, a systematic proteomic survey of human CD34+ cells collected from human umbilical cord blood was performed, in which
C Duszka et al.
The Journal of nutrition, 126(10), 2550-2556 (1996-10-01)
The purposes of this study were to determine the location of beta-carotene dioxygenase (EC 1.13.11.21) activity within the rat gastrointestinal tract, within the villus and within enterocytes, and to identify the metabolites produced in each intestinal fraction. In Wistar female
J R Kanofsky et al.
Photochemistry and photobiology, 73(4), 349-358 (2001-05-03)
A cationic carotenoid derivative (GRP-carotenal) was synthesized by the reaction of Girard's reagent P and beta-apo-8'-carotenal. The singlet-oxygen quenching constants for GRP-carotenal were 1.3 +/- 0.1 x 10(10) and 1.0 +/- 0.1 x 10(10) M-1 s-1 in acetonitrile and in
G Drikos et al.
European biophysics journal : EBJ, 16(4), 193-205 (1988-01-01)
During the visual process, light absorption in the 11-cis retinylidene chromophore leads to a rapid cis-trans-isomerization which initiates the phototransduction step. Important spectroscopic properties of this chromophore can be derived from polarized UV-absorption spectra of crystalline 11-cis-retinal if a parallel
Exibir todos os documentos relacionados

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica