GIBBERELLIC ACID

Code: PHR1567-500MG D2-231

Analysis Note

These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.

Application

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€175.89 500MG
€216.34 inc. VAT

Analysis Note

These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.

Application

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Gibberellic Acid may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by high performance liquid chromatography (HPLC) and fluorometric techniques.

Biochem/physiol Actions

Phytohormone that controls important aspects of plant growth: germination, elongation, and flowering. The effects are mediated by inducing degradation of the DELLA repressor protein, and probably other minor signalling pathways.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAA4483 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

General description

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.Gibberellic Acid is produced because of the metabolism of Gibberella fujikuroi (imperfect stage, Fusarium moniliforme). It is known as a growth substance for plants. Owing to its influence on growth rate as well as morphology of plants, and flower induction, gibberellic acid has been extensively synthesized by chemical and pharmaceutical industries.

Gibberellic acid is an endogenous plant growth regulator

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

agencytraceable to USP 1291005
application(s)pharmaceutical (small molecule)
CofAcurrent certificate can be downloaded
formatneat
gradepharmaceutical secondary standard, certified reference material
InChI keyIXORZMNAPKEEDV-OBDJNFEBSA-N
InChI1S/C19H22O6/c1-9-7-17-8-18(9,24)5-3-10(17)19-6-4-11(20)16(2,15(23)25-19)13(19)12(17)14(21)22/h4,6,10-13,20,24H,1,3,5,7-8H2,2H3,(H,21,22)/t10-,11+,12-,13-,16-,17+,18+,19-/m1/s1
packagingpkg of 500 mg
Quality Level300
SMILES stringC[C@]12[C@@H](O)C=C[C@@]3(OC1=O)[C@@H]4CC[C@]5(O)C[C@]4(CC5=C)[C@H]([C@H]23)C(O)=O
storage temp.2-30°C
technique(s)gas chromatography (GC): suitable, HPLC: suitable
Cas Number77-06-5
This product has met the following criteria to qualify for the following awards:



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