Sodium 2-biphenylate

Base Information

• Chemical Name: Sodium 2-biphenylate
• CAS No.: 132-27-4
• Molecular Formula: C12H9NaO
• Molecular Weight: 192.193
• Hs Code.: 29071990
• Mol file: 132-27-4.mol

Synonyms:2-Biphenylol,sodium salt (8CI);Phenol, o-phenyl-, sodium deriv. (6CI);[1,1'-Biphenyl]-2-ol, sodium salt (9CI);2-Hydroxydiphenyl sodium;2-Phenylphenol sodium salt;Deccosol;Dowicide;Dowicide A;Microban P 2;Mystox WFA;Natriphene;Preventol ON extra;SOPP;2-Biphenylol sodium salt;Sodium 2-hydroxydiphenyl;Sodium 2-phenylphenate;Sodium 2-phenylphenoate;Sodium 2-phenylphenol;Sodium o-phenylphenate;Sodium o-phenylphenol;Sodiumo-phenylphenoxide;Stopmold B;o-Phenylphenol sodium salt;[1,1'-Biphenyl]-2-ol,sodium salt (1:1);

Chemical Property of Sodium 2-biphenylate

Chemical Property:

• Appearance/Colour: light brown or beige solid
• Vapor Pressure: 1.2Pa at 20℃
• Melting Point: 59 °C
• Boiling Point: 282 °C at 760 mmHg
• PKA: 9.9 (acid)
• Flash Point: 140.3 °C
• PSA: 23.06000
• Density: 1.213 g/cm³
• LogP: 3.49740
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility.: 1220 g kg-1 (35 °C)

Purity/Quality:

99% ^*data from raw suppliers

Sodium 2-biphenylate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn, N
• Hazard Codes: Xn,N
• Statements: 22-37/38-41-50
• Safety Statements: 22-26-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Uses: Antimicrobial additive in the manufacture of adhesives, leather, metalworking fluids, and textiles; preservative in automotive polishes, ceramic glazes, laundry starch, inks, floor wax emulsions; agricultural fungicide.

Technology Process of Sodium 2-biphenylate

There total 2 articles about Sodium 2-biphenylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

2-Phenylphenol (90-43-7,287950-96-3) → sodium 2-biphenylate (132-27-4)

Guidance literature:

With sodium; benzene;

DOI:10.1021/ja01306a042

Reference yield:

→ sodium 2-biphenylate (132-27-4)

Guidance literature:

Reference yield: 62.0%

sodium 2-biphenylate (132-27-4) + cyclohexane-1,2-epoxide (286-20-4) → (+/-)-trans-2-(2-phenylphenoxy)cyclohexan-1-ol

Guidance literature:

In water; for 4h; Heating;

DOI:10.1016/0957-4166(95)00029-O

upstream raw materials:

2-Phenylphenol

Downstream raw materials:

1-(Biphenyl-2-yloxy)-3,3,5,5-tetrachloro-1λ⁴,3λ⁵,5λ⁵-[1,2,4,6,3,5]thiatriazadiphosphinine

2-hydroxy-5-(phenylazo)biphenyl

1-(o-Phenyl-phenoxy)-4-phenoxy-benzol

3-phenylsalicylic acid

Refernces

• 1、 -. "Palatable solid pesticidal compositions of ethylene and vinyl acetate copolymer". . . Retrieved 2008/06/13.