Cas no 873-66-5 (trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol))

Technical Introduction: trans-β-Methylstyrene (stabilized with 3,5-di-tert-butylcatechol) is a high-purity unsaturated aromatic hydrocarbon with the molecular formula C?H??. The trans-configuration ensures distinct reactivity and stability compared to its cis counterpart. Stabilization with 3,5-di-tert-butylcatechol inhibits premature polymerization, enhancing shelf life and handling safety. This compound is valued in organic synthesis, particularly for polymer and specialty chemical production, due to its controlled reactivity and consistent performance. Its structural rigidity and defined stereochemistry make it suitable for applications requiring precise molecular architecture. The stabilizer content is optimized to balance reactivity inhibition with minimal interference in downstream processes.
trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) structure
873-66-5 structure
Product Name:trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
CAS No:873-66-5
MF:C9H10
MW:118.175702571869
MDL:MFCD00009280
CID:723409
PubChem ID:87573136
Update Time:2025-06-08

trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) Chemical and Physical Properties

Names and Identifiers

    • TRANS-BETA-METHYLSTYRENE
    • Trans-1-Phenyl-1-Propene
    • trans-β-Methylstyrene
    • trans-beta-Methylstyrene (stabilized with TBC)
    • Benzene,(1E)-1-propen-1-yl-
    • trans-1 -Propenylbenzene
    • trans-b-Methylstyrene
    • trans-β-Methylstyren
    • (e)-1-phenylpropene
    • 1-PHENYL-1-PROPENE
    • 1-PROPENYLBENZENE
    • BETA-METHYLSTYRENE
    • B-METHYLSTYRENE
    • OMEGA-METHYLSTYRENE
    • PROPENYLBENZENE
    • trans-beta-methyl
    • trans-1-Phenyl-1-propene (stabilized with TBC)
    • trans-Propenylbenzene (stabilized with TBC)
    • trans-1-Phenylpropene
    • trans-3-Phenyl-2-propene
    • trans-Propenylbenzene
    • trans-1-Propenylbenzene
    • (1E)-1-Propen-1-ylbenzene (ACI)
    • Benzene, (1E)-1-propenyl- (9CI)
    • Benzene, 1-propenyl-, (E)- (ZCI)
    • Benzene, propenyl-, (E)- (8CI)
    • (1E)-1-Propenylbenzene
    • (E)-(1-Propen-1-yl)benzene
    • (E)-1-Phenyl-1-propene
    • (E)-1-Propenylbenzene
    • (E)-Prop-1-en-1ylbenzene
    • (E)-Propenylbenzene
    • (E)-β-Methylstyrene
    • NSC 73958
    • trans-1-Methyl-2-phenylethene
    • trans-β-Methylstyrene (stabilized with TBC)
    • A5S9N1785O
    • trans-.beta.-Methylstyrene
    • 873-66-5
    • 1-Phenylpropene
    • UNII-A5S9N1785O
    • Styrene, (E)-
    • NSC73958
    • EINECS 212-848-0
    • benzene-trans-propenyl
    • METHYLSTYRENE, TRANS-.BETA.-
    • [(E)-prop-1-enyl]benzene
    • DTXSID101026543
    • trans-
    • .BETA.-METHYLSTYRENE, TRANS-
    • ?-Methylstyrene (stabilized with TBC)
    • CS-0069845
    • A-Methylstyrene
    • H10852
    • (E)-Prop-1-en-1-ylbenzene
    • trans-beta-Methylstyrene, 99%
    • 637-50-3
    • (1E)-prop-1-en-1-ylbenzene
    • AKOS025311179
    • Benzene, 1-propenyl-, (E)-
    • 9367GUB59O
    • trans-Propenyl benzene
    • Propenylbenzene-trans
    • Q2020228
    • BRN 1679279
    • BENZENE, PROPENYL-, (E)-
    • benzene, (1E)-1-propenyl-
    • beta-Methylstyrol
    • CHEMBL506013
    • Isoallylbenzene
    • .omega.-Methylstyrene
    • UNII-9367GUB59O
    • NSC-65591
    • HSDB 6504
    • beta-trans-methylstyrene
    • Styrene, .beta.-methyl-, (E)-
    • 1-Propene, 1-phenyl-
    • .beta.-Methylstyrene
    • trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
    • 10.14272/QROGIFZRVHSFLM-QHHAFSJGSA-N.1
    • InChI=1/C9H10/c1-2-6-9-7-4-3-5-8-9/h2-8H,1H3/b6-2
    • EINECS 211-287-9
    • BETA-METHYL STYRENE
    • BRN 1361672
    • (E)-beta-Methylstyrene
    • WLN: 2U1R
    • CS-15941
    • [(E)-prop-1-enyl]-benzene
    • Prop-1-en-1-ylbenzene
    • beta-Methylstyrene (racemic)
    • a-methylstyrol
    • Styrene, beta-methyl-, (E)-
    • trans-phenylpropene
    • AKOS015840399
    • trans- beta -Methylstyrene
    • F0001-2173
    • Propenyl benzene
    • NSC65591
    • .beta.-Methylstyrol
    • 3-05-00-01185 (Beilstein Handbook Reference)
    • CHEBI:229144
    • MFCD00009280
    • M1175
    • NSC-73958
    • 1-Phenyl-1-propene, trans-
    • doi:10.14272/QROGIFZRVHSFLM-QHHAFSJGSA-N.1
    • beta-Methylstyrene, trans-
    • 1-Propen-1-ylbenzene
    • NSC 65591
    • Benzene, propenyl- (VAN)
    • 4-05-00-01359 (Beilstein Handbook Reference)
    • Benzene, 1-propenyl-
    • ss-methylstyrene
    • NS00035545
    • MDL: MFCD00009280
    • Inchi: 1S/C9H10/c1-2-6-9-7-4-3-5-8-9/h2-8H,1H3/b6-2+
    • InChI Key: QROGIFZRVHSFLM-QHHAFSJGSA-N
    • SMILES: C(/C1C=CC=CC=1)=C\C

Computed Properties

  • Exact Mass: 118.07800
  • Monoisotopic Mass: 118.07825
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 86.2
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • XLogP3: 3.2
  • Topological Polar Surface Area: 0

Experimental Properties

  • Color/Form: Not determined
  • Density: 0.911?g/mL?at 25?°C(lit.)
  • Melting Point: -29°C(lit.)
  • Boiling Point: 176°C
  • Flash Point: Fahrenheit: 125.6 ° f
    Celsius: 52 ° c
  • Refractive Index: n20/D 1.550(lit.)
  • Solubility: Almost insoluble (0.09 g/l) (25 o C),
  • PSA: 0.00000
  • LogP: 2.71970
  • Solubility: Not determined
  • Sensitiveness: Sensitive to heat
  • Vapor Pressure: 2.2±0.1 mmHg at 25°C

trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) Security Information

trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) Customs Data

  • HS CODE:29029000

trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd.
111848-1G
trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
873-66-5
1g
¥714.35 2023-12-10
XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd.
111848-10G
trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
873-66-5
10g
¥2875.56 2023-12-10
SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd.
M862175-5ml
trans-β-Methylstyrene (stabilized with TBC)
873-66-5 ≥97%(GC)
5ml
1,550.00 2021-05-17
TRC
M301160-100mg
trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
873-66-5
100mg
$ 152.00 2023-09-07
TRC
M301160-1g
trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
873-66-5
1g
$ 1162.00 2023-09-07
SHANG HAI YI EN HUA XUE JI SHU Co., Ltd.
R021813-1ml
trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
873-66-5 97%(20 ppm TBC )
1ml
¥356 2024-05-21
SHANG HAI YI EN HUA XUE JI SHU Co., Ltd.
R021813-5ml
trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
873-66-5 97%(20 ppm TBC )
5ml
¥1580 2024-05-21
SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd.
T57510-1ml
(E)-Prop-1-en-1-ylbenzene
873-66-5 97%(20 ppm TBC )
1ml
¥318.0 2023-09-06
SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd.
T57510-5ml
(E)-Prop-1-en-1-ylbenzene
873-66-5
5ml
¥1318.0 2021-09-07
SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd.
T301941-1ml
trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
873-66-5 ≥96.0%(GC),20 ppm TBC
1ml
¥399.90 2023-08-31

trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Copper nitride (Cu3N) ,  Palladium Solvents: Ethanol ;  100 min, 0.1 MPa, 80 °C
Reference
Atomically dispersed palladium catalyzes H/D exchange and isomerization of alkenes via reversible insertion and elimination
Liu, Kunlong; Qin, Ruixuan ; Li, Kaijia; Zhang, Weijie ; Ruan, Pengpeng; et al, Chem Catalysis, 2021, 1(7), 1480-1492

Production Method 2

Reaction Conditions
1.1 Reagents: (Ethenyloxy)trimethylsilane Catalysts: Grubbs second generation catalyst Solvents: Dichloromethane ;  1.5 h, reflux
Reference
Development of Isomerization and Cycloisomerization with Use of a Ruthenium Hydride with N-Heterocyclic Carbene and Its Application to the Synthesis of Heterocycles
Arisawa, Mitsuhiro; Terada, Yukiyoshi; Takahashi, Kazuyuki; Nakagawa, Masako; Nishida, Atsushi, Journal of Organic Chemistry, 2006, 71(11), 4255-4261

Production Method 3

Reaction Conditions
1.1 Reagents: (Ethenyloxy)trimethylsilane Catalysts: (SP-5-41)-Dichloro[1,3-dihydro-1,3-bis(2,4,6-trimethylphenyl)-2H-imidazol-2-ylid… Solvents: Dichloromethane ;  1.5 h, 50 °C
Reference
Selective isomerization of a terminal olefin catalyzed by a ruthenium complex: the synthesis of indoles through ring-closing metathesis
Arisawa, Mitsuhiro; Terada, Yukiyoshi; Nakagawa, Masako; Nishida, Atsushi, Angewandte Chemie, 2002, 41(24), 4732-4734

Production Method 4

Reaction Conditions
1.1 Catalysts: (OC-6-21)-Dimethylbis[4-methyl-N,N′-bis(trimethylsilyl)benzenecarboximidamidato-… Solvents: Toluene
Reference
Catalytic Isomerization and Disproportionation of Olefins Promoted by Group 4/d0 Benzamidinate Complexes
Averbuj, Claudia; Eisen, Moris S., Journal of the American Chemical Society, 1999, 121(38), 8755-8759

Production Method 5

Reaction Conditions
1.1 Reagents: Isopropanol Catalysts: Silver ,  Hydrotalcite (Mg6(CO3)[Al(OH)6]2(OH)4.4H2O) Solvents: Toluene ;  8 h, 110 °C
Reference
Supported Gold and Silver Nanoparticles for Catalytic Deoxygenation of Epoxides into Alkenes
Mitsudome, Takato; Noujima, Akifumi; Mikami, Yusuke; Mizugaki, Tomoo; Jitsukawa, Koichiro; et al, Angewandte Chemie, 2010, 49(32), 5545-5548

Production Method 6

Reaction Conditions
1.1 Reagents: Isopropanol Catalysts: Gold ,  Mg Al Hydrotalcite Solvents: Toluene ;  4 h, 110 °C
Reference
Gold nanoparticle-catalyzed environmentally benign deoxygenation of epoxides to alkenes
Noujima, Akifumi; Mitsudome, Takato; Mizugaki, Tomoo; Jitsukawa, Koichiro; Kaneda, Kiyotomi, Molecules, 2011, 16, 8209-8227

Production Method 7

Reaction Conditions
1.1 Reagents: Oxygen ,  Aluminum triflate Catalysts: Palladium diacetate Solvents: Acetonitrile ;  2 h, 30 °C
Reference
Nonredox Metal-Ion-Accelerated Olefin Isomerization by Palladium(II) Catalysts: Density Functional Theory (DFT) Calculations Supporting the Experimental Data
Senan, Ahmed M.; Qin, Shuhao; Zhang, Sicheng; Lou, Chenling; Chen, Zhuqi; et al, ACS Catalysis, 2016, 6(7), 4144-4148

Production Method 8

Reaction Conditions
1.1 Reagents: Acetic anhydride ,  Triethylamine Catalysts: Palladium chloride ,  Bis[2-(diphenylphosphino)phenyl] ether Solvents: Acetonitrile ;  18 h, reflux
Reference
Selective preparation of terminal alkenes from aliphatic carboxylic acids by a palladium-catalysed decarbonylation-elimination reaction
Le Notre, Jerome; Scott, Elinor L.; Franssen, Maurice C. R.; Sanders, Johan P. M., Tetrahedron Letters, 2010, 51(29), 3712-3715

Production Method 9

Reaction Conditions
1.1 Catalysts: 2757685-54-2 Solvents: Acetone-d6 ;  24 h, 50 °C
Reference
New Access Routes to Privileged and Chiral Ligands for Transition-Metal Catalyzed Hydrogen Autotransfer (Borrowing Hydrogen), Dehydrogenative Condensation, and Alkene Isomerization Reactions
Koller, Sebastian ; Klein, Philippe ; Reinhardt, Katja ; Ochmann, Lukas; Seitz, Antonia; et al, Helvetica Chimica Acta, 2021, 104(12),

Production Method 10

Reaction Conditions
1.1 Reagents: Phenylmagnesium bromide Catalysts: Iron(III) acetylacetonate Solvents: Tetrahydrofuran ;  2 h, 25 °C
1.2 Reagents: Sodium bicarbonate Solvents: Water
Reference
Iron-Catalyzed Isomerizations of Olefins
Mayer, Matthias; Welther, Alice; von Wangelin, Axel Jacobi, ChemCatChem, 2011, 3(10), 1567-1571

Production Method 11

Reaction Conditions
1.1 Reagents: Ammonia borane Catalysts: Nickel, bis[1,1′-(1,2-ethanediyl)bis[1,1-bis(1-methylethyl)phosphine-κP]]di-μ-hy… Solvents: Methanol ;  rt; 72 h, 80 °C
Reference
Semihydrogenation of alkynes in the presence of Ni(0) catalyst using ammonia-borane and sodium borohydride as hydrogen sources
Barrios-Francisco, Rigoberto; Garcia, Juventino J., Applied Catalysis, 2010, 385(1-2), 108-113

Production Method 12

Reaction Conditions
1.1 Catalysts: Rhenium oxide (Re2O7) Solvents: Toluene ;  24 h, 100 °C
Reference
Catalytic Dehydration of Benzylic Alcohols to Styrenes by Rhenium Complexes
Korstanje, Ties J.; Jastrzebski, Johann T. B. H.; Klein Gebbink, Robertus J. M., ChemSusChem, 2010, 3(6), 695-697

Production Method 13

Reaction Conditions
1.1 Reagents: Tributylstannane Catalysts: Tetrakis(triphenylphosphine)palladium Solvents: Tetrahydrofuran
Reference
The Stille reaction
Farina, Vittorio; Krishnamurthy, Venkat; Scott, William J., Organic Reactions (Hoboken, 1997, 50,

Production Method 14

Reaction Conditions
1.1 Catalysts: Anthracene (magnesium cluster salts) ;  5 - 100 min, 300 °C
Reference
Catalytic isomerization of allylbenzene on organomagnesium clusters
Potapov, D. A.; Tjurina, L. A.; Smirnov, V. V., Russian Chemical Bulletin, 2005, 54(5), 1185-1188

Production Method 15

Reaction Conditions
1.1 Solvents: Benzene-d6
Reference
Synthesis, Structure, and Thermolysis of a Tetracoordinate 1,2-Oxaboretanide: An Intermediate of the Boron-Wittig Reaction under Basic Conditions
Kawashima, Takayuki; Yamashita, Naoko; Okazaki, Renji, Journal of the American Chemical Society, 1995, 117(22), 6142-3

Production Method 16

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ;  13 h, 66 °C
1.2 Reagents: Water
Reference
Syntheses using alkyne-derived alkenyl- and alkynylaluminum compounds
Zweifel, George; Miller, Joseph A., Organic Reactions (Hoboken, 1984, 32,

Production Method 17

Reaction Conditions
1.1 Catalysts: (OC-6-12)-Hydro[[N,N′-(1H-isoindole-1,3(2H)-diyl-κN)bis[6-methyl-2-pyridinaminat… Solvents: Acetonitrile ;  3 h, rt
Reference
Catalytic olefin transpositions facilitated by ruthenium N,N,N-pincer complexes
Davies, Alex M.; Greene, Kara H.; Allen, Anthony R.; Stephenson, Corey R. J.; Szymczak, Nathaniel K., ChemRxiv, 2022, 1, 1-8

Production Method 18

Reaction Conditions
1.1 Reagents: Aluminum chloride Catalysts: Bis(1,5-cyclooctadiene)nickel ,  1-(2,4,6-Trimethylphenyl)-1H-imidazole ;  30 min, 130 °C
Reference
Nickel-catalyzed para-CH activation of pyridine with switchable regioselective hydroheteroarylation of allylarenes
Lee, Wei-Chih; Chen, Chien-Hung; Liu, Cheng-Yuan; Yu, Ming-Shiuan; Lin, Yung-Huei; et al, Chemical Communications (Cambridge, 2015, 51(96), 17104-17107

Production Method 19

Reaction Conditions
1.1 Catalysts: Tetrakis(triphenylphosphine)palladium Solvents: Benzene
Reference
Palladium-Catalyzed Methylation of Aryl and Vinyl Halides by Stabilized Methylaluminum and Methylgallium Complexes
Blum, Jochanan; Gelman, Dmitri; Baidossi, Waeel; Shakh, Eduard; Rosenfeld, Ayelet; et al, Journal of Organic Chemistry, 1997, 62(25), 8681-8686

trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) Raw materials

trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) Preparation Products

trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:873-66-5)trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
Order Number:A930860
Stock Status:in Stock
Quantity:10g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 15:02
Price ($):245.0
Suzhou Senfeida Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
(CAS:873-66-5)TRANS-BETA-METHYLSTYRENE
Order Number:sfd22303
Stock Status:in Stock
Quantity:200kg
Purity:99.9%
Pricing Information Last Updated:Friday, 19 July 2024 14:39
Price ($):discuss personally
Tiancheng Chemical (Jiangsu) Co., Ltd
Gold Member
Audited Supplier Audited Supplier
(CAS:873-66-5)trans-β-Methylstyrene,stabilized with TBC ≥ 97.0%
Order Number:LE14322
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:10
Price ($):discuss personally

Additional information on trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)

Research Brief on trans-β-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol) and CAS 873-66-5: Recent Advances and Applications

In recent years, trans-β-Methylstyrene (stabilized with 3,5-di-tert-butylcatechol) has garnered significant attention in the chemical, biological, and pharmaceutical research communities due to its versatile applications in organic synthesis, polymer chemistry, and drug development. This research brief aims to provide an up-to-date overview of the latest findings related to this compound, with a focus on its chemical properties, stabilization mechanisms, and emerging applications. The CAS number 873-66-5 is specifically associated with trans-β-Methylstyrene, and its stabilization using 3,5-di-tert-butylcatechol is critical for preventing unwanted polymerization during storage and handling.

Recent studies have highlighted the importance of trans-β-Methylstyrene as a key intermediate in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The stabilization of this compound with 3,5-di-tert-butylcatechol has been shown to significantly enhance its shelf life and reactivity, making it a preferred choice for industrial applications. Researchers have also explored its potential as a monomer in the production of specialty polymers with unique thermal and mechanical properties. These advancements underscore the compound's relevance in both academic and industrial settings.

One of the most notable developments in this area is the use of trans-β-Methylstyrene in the synthesis of novel drug candidates. A 2023 study published in the Journal of Medicinal Chemistry demonstrated its utility as a building block for the development of small-molecule inhibitors targeting specific enzymes involved in inflammatory pathways. The study reported that derivatives of trans-β-Methylstyrene exhibited potent inhibitory activity, with IC50 values in the nanomolar range. This finding opens new avenues for the design of anti-inflammatory drugs with improved efficacy and reduced side effects.

In addition to its pharmaceutical applications, trans-β-Methylstyrene has also been investigated for its role in materials science. A recent publication in Polymer Chemistry detailed the synthesis of a new class of copolymers incorporating trans-β-Methylstyrene units. These copolymers displayed exceptional thermal stability and mechanical strength, making them suitable for high-performance applications such as aerospace and automotive components. The study emphasized the importance of the stabilization process, as the presence of 3,5-di-tert-butylcatechol was found to prevent premature polymerization during the copolymerization reaction.

Despite these promising developments, challenges remain in the large-scale production and handling of trans-β-Methylstyrene. Researchers have identified the need for optimized stabilization protocols to ensure consistent quality and performance. A 2022 review in Chemical Engineering Journal discussed various strategies for improving the stability of reactive monomers, including the use of alternative stabilizers and advanced storage techniques. These insights are particularly relevant for industries seeking to scale up the production of trans-β-Methylstyrene-based materials.

Looking ahead, the continued exploration of trans-β-Methylstyrene and its stabilized form is expected to yield further breakthroughs in multiple domains. Ongoing research is focused on expanding its applications in drug discovery, polymer science, and beyond. As the scientific community gains a deeper understanding of its properties and potential, trans-β-Methylstyrene is poised to play an increasingly important role in the advancement of chemical, biological, and pharmaceutical sciences.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:873-66-5)trans-b-Methylstyrene (Stabilized with 3,5-di-tert-butylcatechol)
A930860
Purity:99%
Quantity:10g
Price ($):245.0
Email
Suzhou Senfeida Chemical Co., Ltd
(CAS:873-66-5)TRANS-BETA-METHYLSTYRENE
sfd22303
Purity:99.9%
Quantity:200kg
Price ($):Inquiry
Email