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722197

Sigma-Aldrich

Methyl thiocyanate

97%

Sinónimos:

Thiocyanic acid methyl ester

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About This Item

Fórmula lineal:
CH3SCN
Número de CAS:
556-64-9
Peso molecular:
73.12
EC Number:
209-134-6
MDL number:
MFCD00001830
UNSPSC Code:
12352100
PubChem Substance ID:
329763904
NACRES:
NA.22
form:
liquid
assay:
97%

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.469 (lit.)

density

1.052 g/mL at 25 °C (lit.)

functional group

thiocyanate
thioether

SMILES string

CSC#N

InChI

1S/C2H3NS/c1-4-2-3/h1H3

InChI key

VYHVQEYOFIYNJP-UHFFFAOYSA-N

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pictograms

FlameSkull and crossbones
GHS02,GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

109.9 °F - closed cup

flash_point_c

43.3 °C - closed cup

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Certificados de análisis (COA)

Lot/Batch Number
MKCG2809
MKBZ7189V
MKBX8641V
MKBV0122V
MKBS1012V

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T Ohga et al.
FEMS microbiology letters, 113(1), 63-66 (1993-10-01)
Negative chemotaxis, the movement of organisms away from chemicals, was investigated in Pseudomonas aeruginosa using a rapid videotape method. Digital image processing was used to detect changes in bacterial numbers near the mouth of a capillary containing a test chemical.
Yukari Nagatoshi et al.
The Journal of biological chemistry, 284(29), 19301-19309 (2009-05-08)
Almost all of the chlorine-containing gas emitted from natural sources is methyl chloride (CH(3)Cl), which contributes to the destruction of the stratospheric ozone layer. Tropical and subtropical plants emit substantial amounts of CH(3)Cl. A gene involved in CH(3)Cl emission from
Violetta Shestivska et al.
Rapid communications in mass spectrometry : RCM, 25(17), 2459-2467 (2011-08-06)
Infection by Pseudomonas aeruginosa (PA) is a major cause of morbidity and mortality in patients with cystic fibrosis (CF). Breath analysis could potentially be a useful diagnostic of such infection, and analyses of volatile organic compounds (VOCs) emitted from PA
G Amiconi et al.
Journal of biochemical and biophysical methods, 11(4-5), 241-249 (1985-10-01)
Two methods for the determination of methionine in proteins have been used to estimate the extent of methionine sulfoxide obtained upon exposure of proteins to oxidizing agents. Both methods are based on prior treatment with cyanogen bromide, which attacks methionines
Elisabeth A Wade et al.
The journal of physical chemistry. A, 115(21), 5319-5323 (2011-05-11)
Methylisothiocyanate (CH(3)NCS) was photolyzed at 193 and 248 nm, and the resulting time-resolved infrared emission was observed. Similar experiments were performed on methylthiocyanate (CH(3)SCN) photolyzed at 193 nm. Previous work suggested that these isomers undergo excited-state isomerization prior to dissociation
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