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(±)-Jasmonic acid

analytical standard

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About This Item

Formula empirica (notazione di Hill):
C12H18O3
Numero CAS:
Peso molecolare:
210.27
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Saggio

≥90.0% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

food and beverages

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

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
ZNJFBWYDHIGLCU-CMIOBCHKSA-N

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Descrizione generale

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

Applicazioni

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

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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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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