Basic Description

Synonyms	(4E)-1-methyl-4-(6-methylhept-5-en-2-ylidene)cyclohexene \| 4PU30 cpd \| NCGC00164383-01 \| Forchlorfenuron (KT-30, CPPU) \| 1-(2-Chloro-4-pyridyl)-3-phenylurea \| AC-11699 \| s5306 \| Forchlorfenuron 10 microg/mL in Methanol \| Forchlorfenuron \| K62IP7463J \| Q-2
Specifications & Purity	for cell culture, ≥98%
Biochemical and Physiological Mechanisms	CPPU is a cytokinin oxidase/dehydrogenase (CKO) inhibitor.Synthetic cytokinin and plant growth regulator. Potent septin polymerization inducer. Promotes cell division and differentiation. Delays senescence. Alters septin organization without affecting act
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Grade	for cell culture
Note	Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description	Forchlorfenuron (CPPU) is a cytokinin that enhances in vitro direct shoot organogenesis of Citrus aurantium L. epicotyl segments.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Pyridines and derivatives
    - Subclass Halopyridines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Pyridines and derivatives
Subclass	Halopyridines
Intermediate Tree Nodes	Not available
Direct Parent	2-halopyridines
Alternative Parents	Benzene and substituted derivatives Aryl chlorides Heteroaromatic compounds Isoureas Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organochlorides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	2-halopyridine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Isourea - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidic acid derivative - Azacycle - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as 2-halopyridines. These are organic compounds containing a pyridine ring substituted at the 2-position by a halogen atom.
External Descriptors	a small molecule
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

Associated Targets(Human)

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504756187
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504756187
IUPAC Name	1-(2-chloropyridin-4-yl)-3-phenylurea
INCHI	InChI=1S/C12H10ClN3O/c13-11-8-10(6-7-14-11)16-12(17)15-9-4-2-1-3-5-9/h1-8H,(H2,14,15,16,17)
InChIKey	GPXLRLUVLMHHIK-UHFFFAOYSA-N
Smiles	C1=CC=C(C=C1)NC(=O)NC2=CC(=NC=C2)Cl
Isomeric SMILES	C1=CC=C(C=C1)NC(=O)NC2=CC(=NC=C2)Cl
WGK Germany	3
RTECS	YS7182500
Molecular Weight	247.68
Beilstein	22(5)9,173
Reaxy-Rn	481338
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=481338&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.

11 results found

Lot Number	Certificate Type	Date	Item
C2408401	Certificate of Analysis	Jan 29, 2024	F118861
C2408382	Certificate of Analysis	Jan 29, 2024	F118861
C2408384	Certificate of Analysis	Jan 29, 2024	F118861
C2408381	Certificate of Analysis	Jan 29, 2024	F118861
C2408383	Certificate of Analysis	Jan 29, 2024	F118861
K22301129	Certificate of Analysis	Nov 14, 2022	F118861
K22301111	Certificate of Analysis	Nov 14, 2022	F118861
K22301117	Certificate of Analysis	Nov 14, 2022	F118861
K2208108	Certificate of Analysis	Nov 11, 2022	F118861
K2201624	Certificate of Analysis	Nov 05, 2022	F118861
D1925063	Certificate of Analysis	Mar 24, 2022	F118861

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Chemical and Physical Properties

Solubility	Soluble in Methanol
Sensitivity	heat sensitive
Melt Point(°C)	172°C
Molecular Weight	247.680 g/mol
XLogP3	2.400
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	247.051 Da
Monoisotopic Mass	247.051 Da
Topological Polar Surface Area	54.000 Å²
Heavy Atom Count	17
Formal Charge	0
Complexity	256.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
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. Baisen Chen, Rongxia Tan, Yufei Hu, Gongke Li. (2023) Chemiluminescence method based on the KIO4−K2CO3−Mn2+ reaction for rapid and sensitive determination of forchlorfenuron in dried fruit. LUMINESCENCE, 38 (9): (1639-1646).
2. Yanmei Ren, Ping Xiang, Qilong Xie, Haixiu Yang, Shuhui Liu. (2021) Rapid analysis of forchlorfenuron in fruits using molecular complex-based dispersive liquid–liquid microextraction. Food Additives and Contaminants Part A-Chemistry Analysis Control Exposure & Risk Assessment, 38 (4): (637-645).
3. Pengfei Li,Yanke Lu,Jiangxue Cao,Mengyuan Li,Chunliu Yang,Hongyuan Yan. (2020-06-09) Imidazolium ionic-liquid-modified phenolic resin for solid-phase extraction of thidiazuron and forchlorfenuron from cucumbers.. Journal of chromatography. A, 1623 (461192-461192).
4. Yueru Wang, Hansong Wang, Jiaxuan Chen, Bolun Mei, Yu Li, Tao Li, Baozeng Ren. (2024) Solid-liquid equilibrium of forchlorfenuron in four binary solvents: Experiments, hansen solubility parameter and molecular simulation. JOURNAL OF MOLECULAR LIQUIDS, 403 (124739).

Solution Calculators

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SKU	Size	Availability	Price
F118861-1g	1g	3	$25.90
F118861-5g	5g	3	$96.90
F118861-25g	25g	1	$228.90
F118861-100g	100g	1	$820.90

Forchlorfenuron - for cell culture，98%, high purity , CAS No.68157-60-8