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MEPHENESIN

CAS No.
59-47-2
Chemical Name:
MEPHENESIN
Synonyms
Rhex;Sinan;Tolax;Xeral;a1141;Ortol;A 1141;Daserd;Glytol;Mephin
CBNumber:
CB5210066
Molecular Formula:
C10H14O3
Molecular Weight:
182.22
MDL Number:
MFCD00004718
MOL File:
59-47-2.mol
MSDS File:
SDS
Last updated:2024-04-25 17:59:01

MEPHENESIN Properties

Melting point 69-71 °C(lit.)
Boiling point 153-154 °C4 mm Hg(lit.)
Density 1.0966 (rough estimate)
refractive index 1.5320 (estimate)
Flash point 153-154°C/4mm
storage temp. Sealed in dry,Room Temperature
solubility Soluble in alcohol
pka 13.52±0.20(Predicted)
form Solid
color White
Merck 14,5850
EWG's Food Scores 1
FDA UNII 7B8PIR2954
ATC code M03BX06

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Warning
Hazard statements  H301
Precautionary statements  P264-P270-P301+P310a-P321-P405-P501a
Hazard Codes  Xn
Risk Statements  22-36
Safety Statements  26
WGK Germany  2
RTECS  TZ1225000
HS Code  2909498090
Toxicity LD50 in mice, rats, hamsters (mg/kg): 471, 283, 322 i.p.; 990, 945, 821 orally (Roszkowski); LD50 in mice (mM/kg): 2.83 i.p.; 10.53 orally (Dresel, Slater)
NFPA 704
1
2 0

MEPHENESIN price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich S423300 3-(ORTHO-TOLYLOXY)-1,2-PROPANEDIOL Aldrich 59-47-2 1g $179 2024-03-01 Buy
TCI Chemical M3076 Mephenesin >98.0%(GC) 59-47-2 25g $31 2024-03-01 Buy
TRC M225013 Mephenesin 59-47-2 250mg $50 2021-12-16 Buy
Chem-Impex 38082 Mephenesin,≥98%(GC) ≥98%(GC) 59-47-2 25G $43.1 2021-12-16 Buy
ChemScene CS-5340 Mephenesin 99.20% 59-47-2 500mg $50 2021-12-16 Buy
Product number Packaging Price Buy
S423300 1g $179 Buy
M3076 25g $31 Buy
M225013 250mg $50 Buy
38082 25G $43.1 Buy
CS-5340 500mg $50 Buy

MEPHENESIN Chemical Properties,Uses,Production

Originator

Tolserol,Squibb,US,1948

Uses

muscle relaxant (skeletal)

Uses

Mephenesin was used in the study of ligand-based virtual screening and design of antimalarial compounds.

Definition

ChEBI: 1-(2-methylphenyl)glycerol is a glycerol ether in which a single 2-methylphenyl group is attached at position 1 of glycerol via an ether linkage. It is an aromatic ether and a glycerol ether. It is functionally related to an o-cresol.

Manufacturing Process

Into an iron or copper reaction vessel having an efficient stirring device and furnished with a refluxing column and condenser, were charged 330 lb of high quality meta-cresol and 150 lb of glycerol, together with 25 lb of sodium acetate to serve as the catalyst in the reaction. The reaction mixture, of this composition, was then heated to 250°C. The water of the reaction distilled off during the heating as the ether formation proceeded, this removal of water from the reaction chamber being promoted by the presence of the excess of phenol, some of which also continued to distill over. Towards the end of the reaction, after about 12 hours, when about 60% of the glycerol had been converted, at which point the reaction slowed down and the distillate was mainly cresol, the batch was cooled and 50 gallons of water were added to it along with 150 lb of xylene. As the result of these additions and the cooling down of the material the batch stratified into an aqueous layer containing unreacted glycerol, polyglycerols and sodium acetate, and a nonaqueous layer containing the ethers that had been formed in the reaction, together with unreacted cresol which remained in the reaction chamber, dissolved in the xylene that had been added to the batch. The aqueous layer was then separated and the water content removed therefrom by evaporation to a degree suitable for the recovery of the glycerol and sodium acetate contents of the layer, for their reuse in the process in a succeeding batch therein. The separated nonaqueous layer containing the ethers was distilled to recover the xylene and cresol contents respectively as the early fractions of the layer thus subjected to distillation. The cresol thus recovered, together with the cresol recovered from the distillate obtained during the heating of the reaction mixture, was returned to the process for reuse in a succeeding batch. Redistillation of the ether mixture recovered is usually necessary and desirable, particularly from the point of view of removing last traces of cresol therefrom. The yield of mixed ethers in this example was about 200 lb, in the relative proportions stated of about 70 parts of monoether to 30 of diether.

brand name

Tolserol (Bristol-Myers Squibb);Bioglan m/q;Decontracyl-baum;Geno-sal;Glykresinum;Glyptol;Kencaps;Mefentil;Mepha-gesic;Mephesol;Midisalb-m;Myocalm;Myolisysin;Neo-xoline-m;Nochyrol;Relaxil-g;Rhex "hobein";Salimed compound;Walconesin.

Therapeutic Function

Muscle relaxant

World Health Organization (WHO)

Mephenesin, a centrally acting muscle relaxant and sedative, was introduced in 1948 and its use has subsequently been associated with some of the undesirable features of barbiturate use. It is of limited efficacy since it is shortacting and does not relieve the spasticity associated with chronic neurological disorders. It has therefore been largely superseded by benzodiazepines but it remains available in some countries.

MEPHENESIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 108)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Mojin Biotechnology Co., Ltd
+8613288715578 sales@hbmojin.com China 12468 58
Ouhuang Engineering Materials (Hubei) Co., Ltd
+8617702722807 admin@hbouhuang.com China 3001 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21689 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9341 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282 alice@crovellbio.com China 8829 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Zhengzhou Alfa Chemical Co.,Ltd
+8618530059196 sale04@alfachem.cn China 12770 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
AFINE CHEMICALS LIMITED
0571-85134551 18958018566; info@afinechem.com China 15377 58

View Lastest Price from MEPHENESIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Mephenesin pictures 2024-04-25 Mephenesin
59-47-2
US $5.00 / kg 1kg 99.92% 50000tons Ouhuang Engineering Materials (Hubei) Co., Ltd
MEPHENESIN pictures 2023-08-14 MEPHENESIN
59-47-2
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
MEPHENESIN pictures 2023-03-06 MEPHENESIN
59-47-2
US $1.00 / KG 1KG 99% 100000kg Hebei Guanlang Biotechnology Co,.LTD
  • Mephenesin pictures
  • Mephenesin
    59-47-2
  • US $5.00 / kg
  • 99.92%
  • Ouhuang Engineering Materials (Hubei) Co., Ltd
  • MEPHENESIN pictures
  • MEPHENESIN
    59-47-2
  • US $0.00 / KG
  • 99%
  • Hebei Mojin Biotechnology Co., Ltd
  • MEPHENESIN pictures
  • MEPHENESIN
    59-47-2
  • US $1.00 / KG
  • 99%
  • Hebei Guanlang Biotechnology Co,.LTD
1,2-Propanediol, 3-(2-methylphenoxy)- 1,2-Propanediol, 3-(o-tolyloxy)- 1-Ortho-tolylglycerol ether 1-ortho-tolylglycerolether 1-o-Tolylglycerol ether 3-(2-Tolyloxy)-1,2-propanediol 3-(o-Methylphenoxy)-1,2-propanediol 3-(o-tolyloxy)-2-propanediol 3-(o-Tolyloxy)propane-1,2-diol A 1141 Cresossipropandiolo Cresoxydiol Curaril Curarythan Curythan Daserd Daserol Decontractil Decontractyl Diloxol Dioloxal Dioloxol Findolar Findolor Glukresin Glyceryl o-Tolyl ether glycerylo-tolylether Glykresin Glyotol Glytol Halabar Kinavosyl Kresoxypropandiol Lissenphan Lissephen Mc 2303 Mefenesina Mefensina Memphenesin Mephate Mephedan Mephelor Mephenesine Mephensin Mepherol Mephesin Mephin Mephosal Mephson Mervaldin Mianesina Miolisina Moctynol Myanesin Myanil Myanol Myasin Myastenin