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Thiocyanatomethyl thiocyanate

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Identification
Molecular formula
C3N2S2
CAS number
2031-99-4
IUPAC name
thiocyanatomethyl thiocyanate
State
State

At room temperature, thiocyanatomethyl thiocyanate is in a solid state.

Melting point (Celsius)
41.00
Melting point (Kelvin)
314.15
Boiling point (Celsius)
213.00
Boiling point (Kelvin)
486.15
General information
Molecular weight
129.21g/mol
Molar mass
129.2070g/mol
Density
1.4200g/cm3
Appearence

Thiocyanatomethyl thiocyanate is a solid compound with a crystalline structure. It typically appears as colorless to slightly pale yellow crystals.

Comment on solubility

Solubility of Thiocyanatomethyl Thiocyanate

Thiocyanatomethyl thiocyanate, with the chemical formula C2H2N2S2, presents intriguing solubility characteristics that merit discussion. Its solubility properties are influenced by several factors, including:

  • Polarity: The presence of both thiocyanate groups (–SCN) contributes to the compound's polar nature, which can enhance solubility in polar solvents.
  • Hydrogen Bonding: Its ability to form hydrogen bonds can favor its solubility in solvents containing active hydrogen, such as water.
  • Solvent Interactions: The solubility is often greater in solvents that can stabilize the thiocyanate ions, such as dimethyl sulfoxide (DMSO) or other aprotic solvents.

In general, thiocyanatomethyl thiocyanate is more soluble in polar solvents than in non-polar ones. To illustrate:

  1. Water: Moderate solubility is expected due to polar interactions.
  2. Organic Solvents: Better solubility can be seen in polar organic solvents.

In conclusion, the solubility of thiocyanatomethyl thiocyanate can be considered significant in appropriate solvents, allowing for various applications in chemical processes and research.

Interesting facts

Interesting Facts About Thiocyanatomethyl Thiocyanate

Thiocyanatomethyl thiocyanate, often abbreviated as TMT, is a fascinating compound that plays a role in various chemical contexts. Here are some notable points about this compound:

  • Structure and Composition: This compound contains both thiocyanate groups, which are key in many biochemical and industrial processes. The presence of two thiocyanate functionalities contributes to its unique chemical reactivity and properties.
  • Biological Significance: Thiocyanatomethyl thiocyanate is of interest in biological systems, particularly in research related to cyanide toxicity. The thiocyanate ion can act as a detoxifying agent for cyanide, and compounds like TMT can be studied for their potential protective roles.
  • Industrial Applications: This compound is not only of academic interest but also holds potential in the industrial sector, particularly in the production of pharmaceuticals and agrochemicals. Its reactivity may be harnessed in synthesizing other complex organic molecules.
  • Research Implications: Ongoing research investigates the applications of thiocyanatomethyl thiocyanate in fields like materials science, where its properties can be exploited in developing interesting polymers and other materials.
  • Environmental Considerations: Understanding the behavior and fate of TMT in various environments is crucial, especially given the increasing concern about the impact of industrial chemicals on ecosystems.

In summary, thiocyanatomethyl thiocyanate is a multifaceted compound that bridges the gap between chemistry, biology, and industry. As researchers continue to explore its properties and applications, we can anticipate new and exciting developments stemming from this compound.

Synonyms
Methylene dithiocyanate
6317-18-6
Methylene bis(thiocyanate)
Proxel MB
Methylenedirhodanide
Thiocyanic acid, methylene ester
Methylenedirhodanid
Nalfloc N 206
Dithiocyanatomethane
Methane, dithiocyanato-
METHYLENE THIOCYANATE
Methylendirhodanid
methylenebisthiocyanate
Methylendithiokyanat
Nalco D-1994
Caswell No. 565
Methylene Bisthiocyanate
Slimicide MC
Methylenebis(thiocyanate)
NSC 40464
Methylendirhodanid [Czech]
Methylendithiokyanat [Czech]
Methylenedirhodanid [German]
Antiblu 3737
CCRIS 636
N-948 Biocide
V 709
Busan 110
HSDB 4497
K1QS9QOS1J
Tolcide MBT
EINECS 228-652-3
EPA Pesticide Chemical Code 068102
Thiocyanic acid, C,C'-methylene ester
BRN 1743370
CP 17879
DTXSID8025599
NSC-40464
CH2(SCN)2
DTXCID805599
CHEBI:134614
Methylene ester of Thiocyanic acid
3-03-00-00288 (Beilstein Handbook Reference)
METHYLENE THIOCYANATE [HSDB]
{[(cyanosulfanyl)methyl]sulfanyl}carbonitrile
METHYLENDIRHODANID (CZECH)
Kilstain
METHYLENEDIRHODANID (GERMAN)
Dithiocyanomethane
Basiment 540
Metasol T 10
(((cyanosulfanyl)methyl)sulfanyl)carbonitrile
Antiblu 3738
Bis(thiocyanato)methane
Nalco 5793
Nalco D 2303
Cytox
Amerstat 282
Methane, dithiocyanato
Nalco D1994
Methylene thiocyanic acid
Organiclear, Methylene bisthiocyanate
228-652-3
inchi=1/c3h2n2s2/c4-1-6-3-7-2-5/h3h
Methylenedithiocyanate
thiocyanatomethyl thiocyanate
CAS-6317-18-6
UNII-K1QS9QOS1J
MFCD00001833
methylene bis thiocyanate
WLN: NCS1SCN
Amerstat 282 (Salt/Mix)
SCHEMBL20931
MLS002454417
CHEMBL1524617
NSC40464
Tox21_202325
Tox21_301058
AKOS015915319
thiocyanic acid thiocyanatomethyl ester
FM07826
NCGC00091525-01
NCGC00091525-02
NCGC00091525-03
NCGC00091525-04
NCGC00091525-05
NCGC00091525-06
NCGC00091525-07
NCGC00254960-01
NCGC00259874-01
AS-11804
SMR000778018
DB-054418
M1020
NS00004687
D91426
A834251
Q1963090