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C105198

Sigma-Aldrich

Cyclohexyl isocyanate

98%

Synonym(s):

Isocyanatocyclohexane

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About This Item

Linear Formula:
C6H11NCO
CAS Number:
3173-53-3
Molecular Weight:
125.17
Beilstein:
507983
EC Number:
221-639-3
MDL number:
MFCD00003840
UNSPSC Code:
12352100
PubChem Substance ID:
24891960
NACRES:
NA.22

vapor pressure

1.83 psi ( 20 °C)

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.455 (lit.)

bp

168-170 °C (lit.)

density

0.98 g/mL at 25 °C (lit.)

SMILES string

O=C=NC1CCCCC1

InChI

1S/C7H11NO/c9-6-8-7-4-2-1-3-5-7/h7H,1-5H2

InChI key

KQWGXHWJMSMDJJ-UHFFFAOYSA-N

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Caution

precipitation may occur during storage

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

120.2 °F - closed cup

Flash Point(C)

49 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF2975
BCBJ4058V
1447850
MKBJ7837V
1447850V

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S D Harrison et al.
Cancer chemotherapy and pharmacology, 14(2), 146-149 (1985-01-01)
The effects of BCNU, CCNU, methyl-CCNU, streptozotocin, and chlorozotocin on calmodulin activity were studied in vitro and in vivo. Preincubation of BCNU, CCNU, and methyl-CCNU with calmodulin produced a concentration-dependent inhibition of in vitro calmodulin activity expressed as stimulation of
R E Solís-Correa et al.
Journal of biomaterials science. Polymer edition, 18(5), 561-578 (2007-06-07)
For short-term cardiovascular application, segmented polyurethanes (SPUs) based on 4,4-methylenebis(cyclohexyl isocyanate) (HMDI), polytetramethylenglycol (PTMG) and 1,4-butanediol (BD) were synthesized and characterized by spectroscopy (FT-IR, (1)H-NMR) and thermal (TGA, DMA, DSC) and mechanical techniques. The segmented nature of the SPUs was
Sönke Rehder et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 80(1), 203-208 (2011-09-13)
A glibenclamide polymorph published by Panagopoulou-Kaplani and Malamataris (2000) [1], obtained by sublimation of amorphous glibenclamide, was analysed. A new interpretation of the data is presented and experimentally confirmed by X-ray powder diffractometry, Fourier transformation infrared spectroscopy, differential scanning calorimetry

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