Basic Description

Synonyms	2',6'-Pipecoloxylidide, 1-methyl-, (+)- \| (1S,2S,4aR,4bR,7S,9aR,10S,10aR)-2-Hydroxy-1-methyl-8-methylene-13-oxododecahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid \| 2beta,4a-dihydroxy-1-methyl-8-methylene-4aalpha,4bbeta-gibbane-
Specifications & Purity	≥90%
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Application： Used for its stimulating effect on cell division and cell elongation, seed germination and flowering in long day plants

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Prenol lipids
    - Subclass Diterpenoids
      - Level5 Gibberellins
        Level6 C19-gibberellins
        Level7 C19-gibberellin 6-carboxylic acids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Prenol lipids
Subclass	Diterpenoids
Intermediate Tree Nodes	Gibberellins - C19-gibberellins
Direct Parent	C19-gibberellin 6-carboxylic acids
Alternative Parents	Diterpene lactones Oxepanes Gamma butyrolactones Dicarboxylic acids and derivatives Tetrahydrofurans Secondary alcohols Cyclic alcohols and derivatives Carboxylic acid esters Oxacyclic compounds Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic heteropolycyclic compounds
Substituents	20-norgibberellane-6-carboxylic acid - Diterpene lactone - Caprolactone - Oxepane - Dicarboxylic acid or derivatives - Gamma butyrolactone - Cyclic alcohol - Tetrahydrofuran - Carboxylic acid ester - Lactone - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Carboxylic acid - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Alcohol - Carbonyl group - Organooxygen compound - Organic oxygen compound - Aliphatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as c19-gibberellin 6-carboxylic acids. These are c19-gibberellins with a carboxyl group at the 6-position.
External Descriptors	Gibberellins
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	488186682
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488186682
IUPAC Name	(1R,2R,5R,8R,9S,10R,11S,12S)-12-hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid
INCHI	InChI=1S/C19H24O5/c1-9-7-18-8-10(9)3-4-11(18)19-6-5-12(20)17(2,16(23)24-19)14(19)13(18)15(21)22/h10-14,20H,1,3-8H2,2H3,(H,21,22)/t10-,11-,12+,13-,14-,17-,18+,19-/m1/s1
InChIKey	RSQSQJNRHICNNH-NFMPGMCNSA-N
Smiles	CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O
Isomeric SMILES	C[C@@]12[C@H](CC[C@@]3([C@@H]1[C@@H]([C@]45[C@H]3CC[C@H](C4)C(=C)C5)C(=O)O)OC2=O)O
WGK Germany	3
Molecular Weight	332.39
Reaxy-Rn	14455050
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14455050&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

19 results found

Lot Number	Certificate Type	Date	Item
H2321122	Certificate of Analysis	Jun 10, 2025	G135838
E2310221	Certificate of Analysis	Feb 07, 2025	G135838
E2310229	Certificate of Analysis	Feb 07, 2025	G135838
E2310236	Certificate of Analysis	Feb 07, 2025	G135838
E2310491	Certificate of Analysis	Feb 07, 2025	G135838
E2310233	Certificate of Analysis	Feb 07, 2025	G135838
E2310222	Certificate of Analysis	Feb 07, 2025	G135838
E2310489	Certificate of Analysis	Feb 07, 2025	G135838
F2506531	Certificate of Analysis	Jun 27, 2024	G135838
F2506540	Certificate of Analysis	Jun 27, 2024	G135838
C2214331	Certificate of Analysis	Dec 13, 2023	G135838
C2212425	Certificate of Analysis	Dec 13, 2023	G135838
E2310228	Certificate of Analysis	Nov 22, 2022	G135838
F2419065	Certificate of Analysis	Nov 22, 2022	G135838
F2404022	Certificate of Analysis	Nov 22, 2022	G135838
G1803090	Certificate of Analysis	Apr 14, 2022	G135838
C2212424	Certificate of Analysis	Feb 22, 2022	G135838
C2214304	Certificate of Analysis	Feb 22, 2022	G135838
K2208109	Certificate of Analysis	Feb 22, 2022	G135838

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Chemical and Physical Properties

Solubility	Soluble in methanol or ethanol. Also soluble in aqueous sodium bicarbonate or sodium acetate
Boil Point(°C)	574 °C
Molecular Weight	332.400 g/mol
XLogP3	1.700
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	1
Exact Mass	332.162 Da
Monoisotopic Mass	332.162 Da
Topological Polar Surface Area	83.800 Å²
Heavy Atom Count	24
Formal Charge	0
Complexity	685.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	8
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Documents & Articles

Phytohormones commonly used in tissue culture and their functions

Categories: Technical articles

Tags:

cell culture Vitamins Salt Plant tissue culture Hormones Natural products Biopharmacuticals Biobuffers Plant cell culture

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Lian-Ming ZHANG, Xiao-Ping WEI, Yan-Xi WEI, Jian-Ping LI, Ying ZENG. (2014) Determination of Trace Gibberellin A3 by Magnetic Self-assembly Molecularly Imprinted Electrochemical Sensor. CHINESE JOURNAL OF ANALYTICAL CHEMISTRY, 42 (1580).

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SKU	Size	Availability	Price
G135838-1mg	1mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$49.90
G135838-5mg	5mg	10	$195.90
G135838-25mg	25mg	10	$880.90
G135838-100mg	100mg	6	$3,170.90
G135838-250mg	250mg	4	$7,133.90
G135838-1g	1g	1	$25,679.90

Gibberellin A4 - ≥90%, high purity , CAS No.468-44-0