Skip to Content
Merck
CN

308226

Ethyl isocyanatoformate

90%, technical grade

Synonym(s):

Ethoxycarbonyl isocyanate

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
OCNCO2C2H5
CAS Number:
19617-43-7
Molecular Weight:
115.09
NACRES:
NA.22
PubChem Substance ID:
24858658
UNSPSC Code:
12352100
MDL number:
MFCD00011719
Assay:
90%
Form:
liquid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI

1S/C4H5NO3/c1-2-8-4(7)5-3-6/h2H2,1H3

SMILES string

CCOC(=O)N=C=O

InChI key

VMVZGGPZNHFGKS-UHFFFAOYSA-N

grade

technical grade

assay

90%

form

liquid

refractive index

n20/D 1.408 (lit.)

bp

25 °C/10 mmHg (lit.)

density

1.115 g/mL at 25 °C (lit.)

functional group

amine, isocyanate

storage temp.

2-8°C

Quality Level

100

Related Categories

Application

Ethyl isocyanatoformate was used in the synthesis of ethyl[(phenylamino)carbonyl]carbamate by reacting with aniline.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - 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

3 - Flammable liquids

wgk

WGK 3

flash_point_f

96.8 °F - closed cup

flash_point_c

36 °C - closed cup

ppe

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

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000412768
0000412768
0000361203
0000301059
0000301059

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Lin Zhou et al.
Chemical research in toxicology, 17(3), 416-423 (2004-03-18)
Whereas nitrosation of secondary amines produces nitrosamines, amino acids with primary amino groups and glycine ethyl ester were reported to react with nitrite to give unidentified agents that alkylated 4-(p-nitrobenzyl)pyridine to produce purple dyes and be direct mutagens in the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service