(2H10)-p-Xylene

Base Information

• Chemical Name: (2H10)-p-Xylene
• CAS No.: 41051-88-1
• Molecular Formula: C8D10
• Molecular Weight: 116.088
• Hs Code.: 28459000
• European Community (EC) Number: 255-193-6
• DSSTox Substance ID: DTXSID70194021
• Nikkaji Number: J294.819B
• Wikidata: Q83066748
• Mol file: 41051-88-1.mol

Synonyms:41051-88-1;p-Xylene-d10;(2H10)-p-Xylene;1,2,4,5-tetradeuterio-3,6-bis(trideuteriomethyl)benzene;p-Xylene D10;1,4-Xylene-d10;EINECS 255-193-6;1,4-Di(methyl-d3)benzene-d4;Benzene-1,2,4,5-d4-, 3,6-di(methyl-d3)-;1,4-Dimethylbenzene-d10;1,4-Xylene-D10 99.5 atom % D;[2H10]-1,4-Dimethylbenzene;DTXSID70194021;p-Xylene-d10, 99 atom % D;CS-CE-00809;MFCD00037699;D99434;Benzene-1,2,4,5-d4, 3,6-di(methyl-d3)-;A935671

Chemical Property of (2H10)-p-Xylene

Chemical Property:

• Vapor Pressure: 7.94mmHg at 25°C
• Melting Point: 13 °C
• Refractive Index: n20/D 1.492(lit.)
• Boiling Point: 135 °C(lit.)
• Flash Point: 27.2°C
• PSA: 0.00000
• Density: 0.87g/cm³
• LogP: 2.30340
• Storage Temp.: Store below +30°C.
• Sensitive.: Moisture Sensitive
• Solubility.: 0.2g/l
• Water Solubility.: Insoluble in water.
• XLogP3: 3.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 116.141017778
• Heavy Atom Count: 8
• Complexity: 48.4

Purity/Quality:

98%,99%, ^*data from raw suppliers

P-Xylene-d10 ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn
• Statements: 10-20/21-38
• Safety Statements: 23-36/37

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)C
• Isomeric SMILES: [2H]C1=C(C(=C(C(=C1C([2H])([2H])[2H])[2H])[2H])C([2H])([2H])[2H])[2H]
• Uses: p-Xylene-d10 may be used as an internal standard (IS) for GC/MS analysis of volatile organic compounds in the emissions from a landfill.

Technology Process of (2H10)-p-Xylene

There total 5 articles about (2H10)-p-Xylene 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:

C18H6N4(1-)*C8(2)H10(1+) → p-xylene-d10 (41051-88-1) + 2,6,9,10-tetracyanoanthracene (80721-78-4)

Guidance literature:

In acetonitrile; at 25 ℃; Rate constant; isotope effects on the rate of electron transfer;

DOI:10.1021/ja00231a053

Reference yield:

para-xylene (106-42-3) → p-xylene-d10 (41051-88-1)

Guidance literature:

With sulfuric acid-d2;

DOI:10.1039/tf9585400959

Reference yield:

C8(2)H10*C4H4N2 → PYRIMIDINE (289-95-2,25247-63-6) + p-xylene-d10 (41051-88-1)

Guidance literature:

In tetrachloromethane; at 34.9 ℃; Equilibrium constant;

upstream raw materials:

para-xylene

Downstream raw materials:

2,5-Dimethylphenol

C₁₅H₇⁽²⁾H₉

C₁₂H₇⁽²⁾H₉O

Refernces

• 1、 Hurst, Derek T.,Thakrar, Usha B.,Wells, Clifford H. J.,Wyer, John. "An N.M.R. Study of Electron Donor-Electron Acceptor Interaction Between Aromatic Hydrocarbons and Diazines". . p. 1313 - 1319. Retrieved 2007/10/02.