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Allylbenzene - 98%, high purity , CAS No.300-57-2

    Grade & Purity:
  • ≥98%
In stock
Item Number
A101037
Grouped product items
SKU Size
Availability
Price Qty
A101037-5ml
5ml
4
$12.90
A101037-25ml
25ml
Available within 1-2 weeks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$48.90
A101037-100ml
100ml
4
$129.90
A101037-500ml
500ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$581.90

Basic Description

Synonyms 3-Phenyl-1-propene | FD14063 | UNII-3VT7C9MEQ9 | Benzene, 2-propenyl- | F0001-0925 | (prop-2-en-1-yl)benzene | STL268883 | 2-Propen-1-yl-benzene | Benzene, 2-propen-1-yl- | 3VT7C9MEQ9 | EINECS 206-095-7 | DTXSID00861855 | NSC18609 | NSC-18609 | Allylbenze
Specifications & Purity ≥98%
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Benzene and substituted derivatives
Alternative Parents Aromatic hydrocarbons  Cyclic olefins  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Monocyclic benzene moiety - Aromatic hydrocarbon - Cyclic olefin - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors Not available

Associated Targets(non-human)

Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Candida albicans (78123 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mus musculus (284745 Activities)
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 488180966
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488180966
IUPAC Name prop-2-enylbenzene
INCHI InChI=1S/C9H10/c1-2-6-9-7-4-3-5-8-9/h2-5,7-8H,1,6H2
InChIKey HJWLCRVIBGQPNF-UHFFFAOYSA-N
Smiles C=CCC1=CC=CC=C1
Isomeric SMILES C=CCC1=CC=CC=C1
WGK Germany 3
RTECS CY2275000
UN Number 3295
Molecular Weight 118.18
Beilstein 1098501
Reaxy-Rn 1098501
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098501&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.

16 results found

Lot Number Certificate Type Date Item
B2321051 Certificate of Analysis Jun 17, 2025 A101037
F2310004 Certificate of Analysis Apr 17, 2025 A101037
F2310001 Certificate of Analysis Mar 03, 2025 A101037
F2310002 Certificate of Analysis Mar 03, 2025 A101037
B2505146 Certificate of Analysis Feb 07, 2025 A101037
J1818031 Certificate of Analysis Apr 10, 2024 A101037
D2425134 Certificate of Analysis Mar 25, 2024 A101037
D2425135 Certificate of Analysis Mar 25, 2024 A101037
D2403650 Certificate of Analysis Mar 25, 2024 A101037
F2310003 Certificate of Analysis May 27, 2023 A101037
E2327642 Certificate of Analysis May 10, 2023 A101037
B2321049 Certificate of Analysis Feb 25, 2023 A101037
B2321059 Certificate of Analysis Feb 25, 2023 A101037
D2120018 Certificate of Analysis Jan 16, 2023 A101037
K2201619 Certificate of Analysis Dec 08, 2021 A101037
L2101010 Certificate of Analysis Dec 08, 2021 A101037

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Chemical and Physical Properties

Refractive Index 1.511
Flash Point(°F) 92 °F
Flash Point(°C) 33℃
Boil Point(°C) 156-157°C
Melt Point(°C) 557 °C
Molecular Weight 118.180 g/mol
XLogP3 3.200
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 2
Exact Mass 118.078 Da
Monoisotopic Mass 118.078 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 9
Formal Charge 0
Complexity 78.000
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

Citations of This Product

1. Dong Li, Kaixuan Wang, Jiahong Tang, Yizhou Zhao, Hanan Elhaes, Muhammad Tahir, Medhat A. Ibrahim, Yujing Li.  (2023)  Efficient photosensitized singlet oxygen generation in two-dimensional perovskite nanosheets via energy transfer.  APPLIED SURFACE SCIENCE,  613  (155991). 
2. Dingxuan Ma, Yaowen Zhang, Huihui Zhao, Kang Liu, Lei Wang.  (2022)  Directing two copper porphyrin based polymers as highly efficient heterogeneous catalysts for styrene oxidation.  APPLIED SURFACE SCIENCE,  571  (151363). 
3. Gaoyi Yi, Jingxia He, Baian Ji, Die Gao, Kailian Zhang, Lujun Wang, Jing Zeng, Zhining Xia, Qifeng Fu.  (2020)  Solvothermal-assisted in situ rapid growth of octadecylamine functionalized polydopamine-based permanent coating as stationary phase for open-tubular capillary electrochromatography.  JOURNAL OF CHROMATOGRAPHY A,  1628  (461436). 
4. Yingpeng Huo, Jiwen Hu, Yuanyuan Tu, Zhenzhu Huang, Shudong Lin, Yangfei Hu, Chao Feng.  (2020)  Platinum-Imidazolyl Schiff Base Complexes Immobilized in Periodic Mesoporous Organosilica Frameworks as Catalysts for Hydrosilylation.  APPLIED ORGANOMETALLIC CHEMISTRY,  34  (8): (e5697). 
5. Hui Lin, Yanhong Tang, Shuang Dong, Ruibo Lang, Hongge Chen.  (2020)  A new monooxygenase from Herbaspirillum huttiense catalyzed highly enantioselective epoxidation of allylbenzenes and allylic alcohols.  Catalysis Science & Technology,  10  (7): (2145-2151). 
6. Xueping Tao, Mengting Su, Panpan Chen, Meiting Yan, Dan Wang, Lan Xia, Li Rao, Zhining Xia, Qifeng Fu.  (2024)  Zirconium(IV) coordination-mediated rapid and versatile post-modification of polydopamine coating as stationary phase for open-tubular capillary electrochromatography.  JOURNAL OF CHROMATOGRAPHY A,  1736  (465415). 

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