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Merck

14631

Supelco

(±)-Jasmonensäure

analytical standard

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About This Item

Empirische Formel (Hill-System):
C12H18O3
CAS-Nummer:
Molekulargewicht:
210.27
MDL-Nummer:
UNSPSC-Code:
85151701
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Assay

≥90.0% (GC)

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

food and beverages

Format

neat

Lagertemp.

2-8°C

SMILES String

CC\C=C/C[C@H]1[C@@H](CCC1=O)CC(O)=O

InChI

1S/C12H18O3/c1-2-3-4-5-10-9(8-12(14)15)6-7-11(10)13/h3-4,9-10H,2,5-8H2,1H3,(H,14,15)/b4-3-/t9-,10-/m0/s1

InChIKey

ZNJFBWYDHIGLCU-CMIOBCHKSA-N

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Allgemeine Beschreibung

(±)-Jasmonic acid is a plant lipid derivative and a naturally available growth regulator found in higher plants.

Anwendung

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

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Analysenzertifikate (COA)

Lot/Batch Number

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Die Dokumentenbibliothek aufrufen

Jasmonic acid distribution and action in plants: regulation during development and response to biotic and abiotic stress.
Creelman AR and Mullet EJ
Proceedings of the National Academy of Sciences of the USA, 92(10), 4114-4119 (1995)
Qingyuan Li et al.
Scientific reports, 6, 36463-36463 (2016-11-08)
Camellia is a well-known ornamental flower native to Southeast of Asia, including regions such as Japan, Korea and South China. However, most species in the genus Camellia are cold sensitive. To elucidate the cold stress responses in camellia plants, we
R A Creelman et al.
Proceedings of the National Academy of Sciences of the United States of America, 89(11), 4938-4941 (1992-06-01)
Jasmonic acid (JA) and its methyl ester, methyl jasmonate (MeJA), are plant lipid derivatives that resemble mammalian eicosanoids in structure and biosynthesis. These compounds are proposed to play a role in plant wound and pathogen responses. Here we report the

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