Skip to Content
MilliporeSigma

901594

Diisopropylcarbodiimide solution

1 M in THF

Synonym(s):

Diisopropylmethanediimine

Slide 1 of 1
Sign In to View Organizational & Contract Pricing.

Select a Size

25 ML

$106.50

100 ML

$274.00

$106.50

List Price$142.00Save 25%
Web-Only Promotion

Available to ship TODAYDetails

Request a Bulk Order
Ships Every 4 weeks

About This Item

Linear Formula:
C7H14N2
CAS Number:
693-13-0
UNSPSC Code:
12352111
NACRES:
NA.22
MDL number:
MFCD00065689

Key Documents

View All Documentation

Skip To

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

SMILES string

N(=C=NC(C)C)C(C)C

InChI

1S/C7H14N2/c1-6(2)8-5-9-7(3)4/h6-7H,1-4H3

InChI key

BDNKZNFMNDZQMI-UHFFFAOYSA-N

form

liquid

reaction suitability

reaction type: Coupling Reactions

concentration

1 M in THF

density

0.870 g/mL

application(s)

peptide synthesis

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
G152247608680303
Diisopropylcarbodiimide solution 1 M in THF

Sigma-Aldrich

901594

Diisopropylcarbodiimide solution

Gentamicin solution Hybri-Max™, 50 mg/mL gentamicin, 0.1 μm filtered, BioReagent, suitable for hybridoma

Sigma-Aldrich

G1522

Gentamicin solution

Formaldehyde solution Molecular Biology, BioReagent, ≥36.0% in H2O (T)

Sigma-Aldrich

47608

Formaldehyde solution

Tetrahydrofuran solution contains 20 % (v/v) 1,2-Propanediol

Sigma-Aldrich

680303

Tetrahydrofuran solution

form

liquid

form

liquid

form

liquid

form

liquid

reaction suitability

reaction type: Coupling Reactions

reaction suitability

-

reaction suitability

-

reaction suitability

-

concentration

1 M in THF

concentration

50 mg/mL gentamicin

concentration

≥36.0% in H2O (T), 36.0-38.0% (aldehyde method)

concentration

-

density

0.870 g/mL

density

1.000 g/cm3

density

1.09 g/mL at 20 °C, 1.09 g/mL at 25 °C (lit.)

density

0.914 g/mL at 25 °C

application(s)

peptide synthesis

application(s)

-

application(s)

-

application(s)

-

Application

Coupling reagent for peptide syntheses.[1][2][3]
DIC (N,N′-Diisopropylcarbodiimide) has been used in combination with 1-hydroxy-7-azabenzotriazole (HOAt) for the coupling of amino acid with N-allylglycine to form N-allylpeptide.[4]
Valuable reagent offered as a solution in tetrahydrofuran for more convenient handling.

comparable product

Product No.
Description
Pricing

38370

DIC, purum, ≥98.0% (GC)

D125407

DIC, 99%

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

supp_hazards

EUH019

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

2.0 °F

flash_point_c

-16.66 °C

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCX5315
MKCG2872
MKCW1383
MKCR3315

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

Stéphane Chantepie et al.
PloS one, 10(7), e0133140-e0133140 (2015-07-29)
Do all traits within an organism age for the same reason? Evolutionary theories of aging share a common assumption: the strength of natural selection declines with age. A corollary is that additive genetic variance should increase with age. However, not
Tetrahedron Letters, 35, 5981-5981 (1994)
Collection of Czechoslovak Chemical Communications, 59, 691-691 (1994)
Cody L Gilleland et al.
Genetics, 201(1), 39-46 (2015-07-15)
A major goal in the study of human diseases is to assign functions to genes or genetic variants. The model organism Caenorhabditis elegans provides a powerful tool because homologs of many human genes are identifiable, and large collections of genetic
P J Weber et al.
Bioorganic & medicinal chemistry letters, 8(6), 597-600 (1999-01-01)
A new method has been developed to synthesize fluorescein labeled peptides, compounds of increasing importance in bioorganic chemistry, cell biology, pharmacology, drug targeting and medicinal chemistry. We show, that 4(5)-carboxyfluorescein is much more efficient than the hitherto predominantly utilized reagents
View All Related Papers

Questions

Reviews

No rating value

Active Filters

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