Cacodylic acid

This time we are going to enter the fascinating world of Cacodylic acid. For a long time, Cacodylic acid has been a topic of great interest to multiple sectors of society. Its relevance has transcended over the years, generating debates, research and diverse opinions. In this article, we aim to thoroughly explore the different aspects related to Cacodylic acid, from its origins to its impact today. Likewise, we will analyze the role that Cacodylic acid plays in our lives and its influence on the world around us. Get ready to immerse yourself in an exciting journey through Cacodylic acid, discovering its importance and its multiple implications.

Cacodylic acid
Structural formula
Ball-and-stick model
Names
Preferred IUPAC name
Dimethylarsinic acid
Other names
Dimethylarsenic acid, Cacodylic acid, Hydroxydimethylarsine oxide, Arsecodile, Ansar, Silvisar, Phytar 560, DMAA, UN 1572
Identifiers
3D model (JSmol)
1736965
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.000.804 Edit this at Wikidata
EC Number
  • 200-883-4
130562
KEGG
RTECS number
  • CH7525000
UNII
UN number 1572
  • InChI=1S/C2H7AsO2/c1-3(2,4)5/h1-2H3,(H,4,5) checkY
    Key: OGGXGZAMXPVRFZ-UHFFFAOYSA-N checkY
  • InChI=1/C2H7AsO2/c1-3(2,4)5/h1-2H3,(H,4,5)
    Key: OGGXGZAMXPVRFZ-UHFFFAOYAP
  • O=(O)(C)C
Properties
C2H7AsO2
Molar mass 137.9977 g/mol
Appearance White crystals or powder
Odor odorless
Density > 1.1 g/cm3
Melting point 192 to 198 °C (378 to 388 °F; 465 to 471 K)
Boiling point > 200 °C (392 °F; 473 K)
66.7 g/100 ml
Solubility soluble in ethanol, acetic acid
insoluble in diethyl ether
Acidity (pKa) 6
−79.9·10−6 cm3/mol
Structure
triclinic,[3] monoclinic[2]
Hazards
GHS labelling:
GHS06: ToxicGHS09: Environmental hazard
Danger
H301, H331, H410
P261, P264, P270, P271, P273, P301+P310, P304+P340, P311, P321, P330, P391, P403+P233, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
4
0
0
Lethal dose or concentration (LD, LC):
23-100 mg/kg (rat and mouse, oral)
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
☒N verify (what is checkY☒N ?)

Cacodylic acid is an organoarsenic compound with the formula (CH3)2AsO2H. With the formula R2As(O)OH, it is the simplest of the arsinic acids. It is a colorless solid that is soluble in water.

Neutralization of cacodylic acid with base gives cacodylate salts, e.g. sodium cacodylate. They are potent herbicides. Cacodylic acid/sodium cacodylate is a buffering agent in the preparation and fixation of biological samples for electron microscopy and in protein crystallography.

History

In the 18th century it was found that combining arsenic trioxide (As2O3) and four equivalents of potassium acetate (CH3CO2K) gives a product called "Cadet's fuming liquid" which contains cacodyl oxide, ((CH3)2As)2O and cacodyl, ((CH3)2As)2.

Early research into "cacodyls" was reported by Robert Bunsen at the University of Marburg. Bunsen said of the compounds,

"The smell of this body produces instantaneous tingling of the hands and feet, and even giddiness and insensibility... It is remarkable that when one is exposed to the smell of these compounds the tongue becomes covered with a black coating, even when no further evil effects are noticeable".

His work in this field led to an increased understanding of the methyl group.

Cacodyl oxide, ((CH3)2As)2O, is often considered the first organometallic compound to be prepared synthetically.

Cacodylic acid and its salts were incorporated into herbicides by a large variety of manufacturers under numerous brand names. APC Holdings Corp. sold cacodylic acid and its salts under the Phytar brand name.[4] The variety Phytar 560G, a mixture of cacodylic acid and sodium cacodylate, was used during the Vietnam War as a defoliant under the name "Agent Blue".[5]

Reactions

Cacodylic acid is a weak acid with a pKa of around 6.25.[6]

Cacodylic acid can be reduced to dimethylarsine , which is a versatile intermediate for the synthesis of other organoarsenic compounds:[7][8]

(CH3)2AsO2H + 2 Zn + 4 HCl → (CH3)2AsH + 2 ZnCl2 + 2 H2O
(CH3)2AsO2H + SO2 + HI → (CH3)2AsI + SO3 + H2O

When treated with hydrogen sulfide, dithiocacodylic acid results:[9]

(CH3)2AsO2H + 2 H2S → (CH3)2AsS2H + 2 H2O

Health effects

Cacodylic acid is highly toxic by ingestion, inhalation, or skin contact. The U.S. EPA states that all forms of arsenic are a serious risk to human health and the United States Agency for Toxic Substances and Disease Registry ranked arsenic as number 1 in its 2001 Priority List of Hazardous Substances at Superfund sites.[10] Arsenic is classified as a Group-A carcinogen.[10]

See also

References

  1. ^ Betz, R.; McCleland, C.; Marchand, H. (2011). "CSD Entry: CADYLA01 : Dimethylarsinic acid". Cambridge Structural Database: Access Structures. Cambridge Crystallographic Data Centre. doi:10.5517/ccx73mv. Retrieved 2021-12-21.
  2. ^ a b Betz, R.; McCleland, C.; Marchand, H. (2011). "The monoclinic polymorph of dimethylarsinic acid". Acta Crystallogr. E. 67 (8): m1013. doi:10.1107/S1600536811025505. PMC 3212109. PMID 22090811.
  3. ^ Trotter, J.; Zobel, T. (1965). "826. Stereochemistry of arsenic. Part XVI. Cacodylic acid". J. Chem. Soc.: 4466–4471. doi:10.1039/JR9650004466.
  4. ^ Stanley A. Greene (2005). Sittig's Handbook of Pesticides and Agricultural Chemicals. William Andrew. p. 132. ISBN 978-0-8155-1903-4.
  5. ^ Committee to Review the Health Effects in Vietnam Veterans of Exposure to Herbicides; Institute of Medicine (1994). Veterans and Agent Orange: Health Effects of Herbicides Used in Vietnam. National Academies Press. pp. 89–90. ISBN 978-0-309-55619-4.
  6. ^ Shin, T.-W., Kim, K., Lee, I.-J. (April 1997). "Spectrophotometric determination of the acid dissociation constants for cacodylic acid and p-Nitrophenol at elevated temperatures". Journal of Solution Chemistry. 26 (4): 379–390. doi:10.1007/BF02767677. ISSN 0095-9782.
  7. ^ Feltham, R. D.; Kasenally, A.; Nyholm, R. S. (1967). "A New Synthesis of Di- and Tri-Tertiary Arsines". Journal of Organometallic Chemistry. 7 (2): 285–288. doi:10.1016/S0022-328X(00)91079-9.
  8. ^ Burrows, G. J. and Turner, E. E., "A New Type of Compound containing Arsenic", Journal of the Chemical Society Transactions, 1920, 1374-1383
  9. ^ Casey, AT; Ham, NS; MacKey, DJ; Martin, RL (1970). "Synthesis and infrared spectra of some dithiocacodylate complexes". Australian Journal of Chemistry. 23 (6): 1117. doi:10.1071/ch9701117.
  10. ^ a b Dibyendu, Sarkar; Datta, Rupali (2007). "Biogeochemistry of Arsenic in Contaminated Soils of Superfund Sites". EPA. United States Environmental Protection Agency. Archived from the original on 17 March 2020. Retrieved 25 February 2018.

Further reading