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Home > Encyclopedia > I,I′-[2,2′-Dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl] dihypoiodite

I,I′-[2,2′-Dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl] dihypoiodite

pharmaceutical raw materials
I,I′-[2,2′-Dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl] dihypoiodite structure

I,I′-[2,2′-Dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl] dihypoiodite 

structure
  • CAS No:

    552-22-7

  • Formula:

    C20H24I2O2

  • Chemical Name:

    I,I′-[2,2′-Dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl] dihypoiodite

  • Synonyms:

    Hypoiodous acid,I,I′-[2,2′-dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl] ester;Thymol iodide;Hypoiodous acid,2,2′-dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl ester;I,I′-[2,2′-Dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl] dihypoiodite;Annidalin;Aristol;Iodistol;Iodosol;Iodothymol;Iosol;Iothymol;Lothymol;Thymiode;Thymiodol;Thymodin;Thymotol;Iodohydromol;NSC 2222;Aristol (iodothymol dimer);8048-66-6

  • Categories:

    Inorganic Chemistry  >  Inorganic Salts

Description

Thymol iodide is a compound of Iodide and Thymol. Thymol iodide acts as a substitute for iodoform[1]. Thymol iodide is an iodine derivative of Thymol (a phenol derived from thyme oil), which is mostly used as mild antiseptic and fungicide[2].

I,I′-[2,2′-Dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl] dihypoiodite Basic Attributes

550.21

550.21

209-007-5

A51HJM3XSU

2222

DTXSID3046081

REDDISH-BROWN OR REDDISH-YELLOW BULKY POWDER|RED-BROWN CRYSTALS

2908199090

Characteristics

18.46000

7.67480

red to brown powder

1.617g/cm3

69ºC

STABILITY

1.616

READILY SOL IN CHLOROFORM, ETHER, COLLODION, FIXED & VOLATILE OILS; SLIGHTLY SOL IN ALCOHOL; INSOL IN ALKALINE SOLN, WATER, GLYCEROL

2-8°C

SLIGHT AROMATIC ODOR

LEAVES A SLIGHT RESIDUE IN CHLOROFORM, ETHER, COLLODION & IN FIXED & VOLATILE OILS; GIVES OFF PURPLE IODINE VAPORS WHEN HEATED ABOVE 100 °C

Safety Information

NONH for all modes of transport

3

34-22

36/37/39-26

C,Xn

Stable, but may be light sensitive. Incompatible with strong oxidizing agents.

P264, P270, P301+P312, P330, P501

H302

|Warning|H302 (95.35%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 43 companies from 2 notifications to the ECHA C&L Inventory.

Drug Information

3. 3= MODERATELY TOXIC: PROBABLE ORAL LETHAL DOSE (HUMAN), BETWEEN 1 OUNCE & 1 PINT (OR 1 LB) FOR 70 KG PERSON (150 LB). /IODIDE SALTS/

SEE THYMOL. PRODUCES GASTRIC PAIN, NAUSEA, VOMITING, CENTRAL HYPERACTIVITY...OCCASIONALLY CONVULSIONS, COMA, CARDIAC & RESP COLLAPSE. /THYMOL/

I,I′-[2,2′-Dimethyl-5,5′-bis(1-methylethyl)[1,1′-biphenyl]-4,4′-diyl] dihypoiodite Use and Manufacturing

Methods of Manufacturing

MADE BY TREATING SOLN OF THYMOL IN SODIUM HYDROXIDE SOLN WITH IODINE-POTASSIUM IODIDE SOLN: MESSINGER, VORTMANN, GERMAN PATENTS 49,739; 52,828; 52,833; BER 22, 2312 (1889).

Uses

Feed additive, antifungal agent.

/THYMOL IODIDE IS/ A MIXTURE OF IODINE DERIVATIVES OF THYMOL, PRINCIPALLY DITHYMOL DIIODIDE. THE OFFICIAL PREPARATION CONTAINS NOT LESS THAN 43% IODINE, WHEN DRIED OVER SULFURIC ACID FOR 18 HOURS.

Hypoiodous acid, I,I'-[2,2'-dimethyl-5,5'-bis(1-methylethyl)[1,1'-biphenyl]-4,4'-diyl] ester: ACTIVE

Computed Properties

Molecular Weight:550.2
XLogP3:8.2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:549.98658
Monoisotopic Mass:549.98658
Topological Polar Surface Area:18.5
Heavy Atom Count:24
Complexity:352
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Related Drugs

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    CAS No.: 552-22-7
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