2-cis,4-trans-Abscisic acid

ALDRICH/862169 - synthetic, 98%

Synonym: (±)-Abscisic acid; (2Z,4E)-5-(1-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl)-3-methyl-2,4-pentadienoic acid; ABA; Dormin

CAS Number: 14375-45-2
Empirical Formula (Hill Notation): C₁₅H₂₀O₄
Molecular Weight: 264.32
MDL Number: MFCD00075619
Linear Formula: C₁₅H₂₀O₄
Product Type: Chemical

Catalog Number	PKG Qty.	Price


45-862169-50MG	50 mg	$35.80 1/EA	Add To Favorites
45-862169-250MG	250 mg	$152.00 1/EA	Add To Favorites

This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 862169-250MG

Properties
Descriptions
Safety Info.
Basic Data

assay	98%
form	powder
InChI	1S/C15H20O4/c1-10(7-13(17)18)5-6-15(19)11(2)8-12(16)9-14(15,3)4/h5-8,19H,9H2,1-4H3,(H,17,18)/b6-5+,10-7-
InChI key	JLIDBLDQVAYHNE-LXGGSRJLSA-N
mp	186-188 °C (lit.)
Quality Level	100
SMILES string	CC(C=CC1(O)C(C)=CC(=O)CC1(C)C)=CC(O)=O
storage temp.	2-8°C

Application:	Chiral Separation of Abscisic Acid: Research demonstrated direct chiral separation of abscisic acid using high-performance liquid chromatography with a phenyl column and a gamma-cyclodextrin mobile phase, advancing the analytical methods essential for studying plant stress hormones (Terashima et al., 2023 ). Xanthine Oxidase Inhibitory Activity: A study including abscisic acid derivatives showed significant xanthine oxidase inhibitory activity, offering potential health benefits and therapeutic applications (Miyata et al., 2019 ). Anticancer Potential: Extracts containing abscisic acid from mangrove endophytic fungi exhibited cytotoxic properties and induced G(0)/G(1) cell cycle arrest and apoptosis in human cancer cells, highlighting their potential in cancer treatment strategies (Zhou et al., 2018 ). Antidiabetic Activity: Extracts involving abscisic acid from an endophytic fungus showed promising antidiabetic activity, potentially improving treatment options for diabetes through natural product research (Uzor et al., 2017 ). Glucose Tolerance and Insulinemia Reduction: A groundbreaking study found that microgram amounts of abscisic acid in fruit extracts significantly improve glucose tolerance and reduce insulin levels in rats and humans, suggesting its use as a dietary supplement for managing diabetes (Magnone et al., 2015 ).
General description:	2-cis,4-trans-Abscisic acid (ABA) is an organic compound used as a starting material in in organic synthesis. It is also used as a chiral auxiliary during asymmetric synthesis. ABA derivatives can be used to control the stereochemistry of reactions by serving as chiral templates that induce the formation of specific products.
Packaging:	50, 250 mg in amber glass bottle

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Purity	98%
mp	186-188 °C (lit.)
Storage Temp.	2-8°C
UNSPSC	12352100

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