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Merck
CN

216836

Tolylene-2,4-diisocyanate

technical grade, 80%

Synonym(s):

2,4-Diisocyanatotoluene, 4-Methyl-1,3-phenylene diisocyanate, 4-Methyl-m-phenylene diisocyanate, BASF LUPRANATE T80, TDI

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About This Item

Linear Formula:
CH3C6H3(NCO)2
CAS Number:
584-84-9
Molecular Weight:
174.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24852980
EC Number:
209-544-5
Beilstein/REAXYS Number:
744602
MDL number:
MFCD00002011

Key Documents

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Product Name

Tolylene-2,4-diisocyanate, technical grade, 80%

InChI key

DVKJHBMWWAPEIU-UHFFFAOYSA-N

InChI

1S/C9H6N2O2/c1-7-2-3-8(10-5-12)4-9(7)11-6-13/h2-4H,1H3

SMILES string

Cc1ccc(cc1N=C=O)N=C=O

grade

technical grade

vapor density

6 (vs air)

vapor pressure

0.03 mmHg ( 25 °C)

assay

80%

autoignition temp.

>1148 °F

expl. lim.

9.5 %

refractive index

n20/D 1.568 (lit.)

bp

115-120 °C/10 mmHg (lit.)

mp

20-22 °C (lit.)

solubility

acetone and ethanol: soluble(lit.)
alcohol: miscible(lit.)
benzene: soluble(lit.)
carbon tetrachloride: miscible(lit.)
chlorobenzene: miscible(lit.)
diethyl ether: miscible(lit.)
kerosene: miscible(lit.)
olive oil: miscible(lit.)

density

1.225 g/mL at 25 °C

functional group

isocyanate

storage temp.

2-8°C

Quality Level

100

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Legal Information

Product of BASF AG (Aktiengesellschaft)

Other Notes

Remainder tolylene 2,6-diisocyanate

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 2

flash_point_f

269.6 °F - closed cup

flash_point_c

132 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
非剧毒-急性毒性1
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Certificates of Analysis (COA)

Lot/Batch Number
SHBK2647
SHBJ6903
SHBH7054
SHBF7507V
SHBD1256V

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Effects of solvent polarity on the reaction of phenol with tolylene-2, 4-diisocyanate.
Yang PF, et al.
Journal of Applied Polymer Science, 123(1), 580-584 (2012)
Zhenbin Zhang et al.
Methods in molecular biology (Clifton, N.J.), 970, 457-467 (2013-01-04)
Capillary electrochromatography (CEC) has been shown to be a promising technique for miniaturized enantioseparations. Here we present the preparation and application of positively charged cellulose derivative-based chiral stationary phases (CSPs) for the CEC separation of enantiomers. The cellulose derivatives were
Gabriel Kiss et al.
Polymers, 12(7) (2020-07-16)
Ester polyurethane (PU) foam waste was reacted at atmospheric pressure in an autoclave and using microwaves with diethylene glycol (DEG) at different PU/DEG ratios in the presence of diethanolamine as a catalyst to find the glycolysis conditions that allow for
Zhifang Yang et al.
Langmuir : the ACS journal of surfaces and colloids, 26(12), 9386-9392 (2010-04-29)
A novel ABA triblock copolymer containing electroactive tetraaniline [(ANI)(4)] and poly(ethylene oxide) (PEO600, M(n) = 600), (ANI)(4)-b-PEO600-b-(ANI)(4), was synthesized by coupling tetraaniline and PEO600 with tolylene 2,4-diisocyanate. FTIR, NMR, and UV-vis spectroscopy were combined to characterize the chemical structure of
Tatiana Kuznetsova et al.
American journal of hypertension, 28(4), 535-545 (2014-09-23)
The cardio-renal interaction occurs via hemodynamic and humoral factors. Noninvasive assessment of renal hemodynamics is currently possible by assessment of renal resistive index (RRI) derived from intrarenal Doppler arterial waveforms as ((peak systolic velocity - end-diastolic velocity)/peak systolic velocity). Limited
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