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Merck
CN

03002

Iodine

puriss., meets analytical specification of Ph. Eur., BP, USP, 99.8-100.5%

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About This Item

Empirical Formula (Hill Notation):
I2
CAS Number:
Molecular Weight:
253.81
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
51472901
EC Number:
231-442-4
MDL number:
Beilstein/REAXYS Number:
3587194
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vapor density

9 (vs air)

Quality Level

vapor pressure

0.31 mmHg ( 25 °C), 1 mmHg ( 38.7 °C)

grade

puriss.

assay

99.8-100.5%

quality

meets analytical specification of Ph. Eur., BP, USP

resistivity

1.3E15 μΩ-cm

impurities

residual solvents, in accordance, ≤0.03% non-volatile matter

bp

184 °C (lit.)

mp

113 °C (lit.)

anion traces

bromide, chloride (as Cl-): ≤250 mg/kg, sulfate (SO42-): ≤50 mg/kg

SMILES string

II

InChI

1S/I2/c1-2

InChI key

PNDPGZBMCMUPRI-UHFFFAOYSA-N

General description

Iodine is a halogen compound. It is mainly present in sodium iodate (NaIO3) and sodium periodate (NaIO4) deposits. Iodine is a part of thyroxin hormone produced by the thyroid gland. It controls the body′s rate of physical and mental development.

Application

Iodine (I2) was used in the following studies:
  • Synthesis of oligonucleotides using a standard Applied Biosystems 392 DNA/RNA Synthesizer.
  • Fabrication of electrochemical solar cells by using the single-walled carbon nanotubes (SWNTs)-modified fluorine-doped tin oxide coated glass (FTO) glass as the working electrode.
  • To compose iodide-based solution, used as the liquid electrolyte in the dye-sensitized solar cells.

It may be used for the trace-labelling of proteins. It may be used for the iodination methods, in which the cationic portion of the iodine molecule bounds to the ring structure of tyrosine. Theoretical efficiency of labelling achieved is 50%.


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Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT RE 1 Oral - STOT SE 3

target_organs

Respiratory system, Thyroid

flash_point_f

Not applicable

flash_point_c

Not applicable

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Regulatory Information

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Matthew J Moorcroft et al.
Nucleic acids research, 33(8), e75-e75 (2005-05-05)
In this paper, we demonstrate in situ synthesis of oligonucleotide probes on poly(dimethylsiloxane) (PDMS) microchannels through use of conventional phosphoramidite chemistry. PDMS polymer was moulded into a series of microchannels using standard soft lithography (micro-moulding), with dimensions <100 microm. The
Photocurrent response from vertically aligned single-walled carbon nanotube arrays.
Bissett MA and Shapter JG.
The Journal of Physical Chemistry C, 114(14), 6778-6783 (2010)
Efficient trace-labelling of proteins with iodine.
A S McFARLANE
Nature, 182(4627), 53-53 (1958-07-05)



Global Trade Item Number

SKUGTIN
148482-25G04061838737953
148482-5G04061838737960
03002-100G04061838617996
03002-1KG04061838618009
03002-25G04061833489666
03002-500G04061838618016
03002-6X100G04061833635858