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54764

Neoxanthin

≥90% (HPLC), antioxidant, solid

Synonym(s):

(3S,3′S,5R,5′R,6R,6′S,9′-cis)-6,7-Didehydro-5′,6′-epoxy-5′,6′-dihydro-β,β-carotene-3,3′,5(6H)-triol, 9′-cis-Neoxanthin

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About This Item

Empirical Formula (Hill Notation):
C40H56O4
CAS Number:
Molecular Weight:
600.87
MDL number:
UNSPSC Code:
12352202
NACRES:
NA.32
Assay:
≥90% (HPLC)
Form:
solid
Quality level:
Pricing and availability is not currently available.
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Product Name

Neoxanthin, ≥90% (HPLC)

Quality Level

assay

≥90% (HPLC)

form

solid

λ

in ethanol

UV absorption

λ: 435-439 nm Amax

storage temp.

−20°C

SMILES string

C/C(C([H])=[C@]=C1[C@](C)(O)C[C@@H](O)CC1(C)C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(/C=C/[C@@]2(O3)[C@@]3(C)C[C@@H](O)CC2(C)C)C

InChI

1S/C40H56O4/c1-29(17-13-19-31(3)21-22-35-36(5,6)25-33(41)27-38(35,9)43)15-11-12-16-30(2)18-14-20-32(4)23-24-40-37(7,8)26-34(42)28-39(40,10)44-40/h11-21,23-24,33-34,41-43H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,24-23+,29-15+,30-16+,31-19+,32-20+/t22?,33-,34-,38+,39+,40-/m0/s1

InChI key

PGYAYSRVSAJXTE-CLONMANBSA-N

Application

Neoxanthin has been used as a reference standard to determine the phenolic content and antioxidant activity of Phaeodactylum tricornutum extracts by high-performance liquid chromatography (HPLC).[1]

Biochem/physiol Actions

Neoxanthin is an allenic xanthophyll[2] and one of the major carotenoids found in plants such as spinach and barley leaves.[3] A trace amount of this pigment is also found in olive oil. Neoxanthin exists as two geometric isomers such as trans-neoxanthin and 9′-cis-neoxanthin. It acts as a precursor of abscisic acid. It plays a role in photoprotection by providing general antioxidant activity.[3] Neoxanthin exhibits apoptotic and anti-proliferative effects.[4]

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1 of 1

This Item
7299452444SML1229
form

solid

form

-

form

solid

form

powder

assay

≥90% (HPLC)

assay

≥97.0% (HPLC)

assay

≥90.0% (HPLC)

assay

≥98% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

UV absorption

λ: 435-439 nm Amax

UV absorption

-

UV absorption

λ: 438-442 nm Amax

UV absorption

-

λ

in ethanol

λ

-

λ

in ethanol

λ

-


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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Andrew A Pascal et al.
Nature, 436(7047), 134-137 (2005-07-08)
In order to maximize their use of light energy in photosynthesis, plants have molecules that act as light-harvesting antennae, which collect light quanta and deliver them to the reaction centres, where energy conversion into a chemical form takes place. The
Molecular approaches toward targeted cancer therapy with some food plant products: On the role of antioxidants and immune microenvironment
Khuda-Bukhsh A R, et al.
Cancer, 191-202 (2021)
Eiichi Kotake-Nara et al.
Cancer letters, 220(1), 75-84 (2005-03-02)
Neoxanthin and fucoxanthin, which have the characteristic structure of 5,6-monoepoxide and an allenic bond, were previously found to reduce the viability of human prostate cancer cells most intensively among 15 dietary carotenoids tested. In the present study, the induction of



Global Trade Item Number

SKUGTIN
415014-5G04061832084398
54764-1MG04061826696750

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