Skip to Content
Merck
CN

U7129

Urea solution

40 % (w/v) in H2O

Synonym(s):

Carbamide, Carbonyldiamide

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
NH2CONH2
CAS Number:
Molecular Weight:
60.06
UNSPSC Code:
12352111
NACRES:
NA.75
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
635724
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


sterility

non-sterile; sterile-filtered

Quality Level

contains

0.1% benzoic acid as preservative

packaging

vial of 5 mL

concentration

40 % (w/v) in H2O

storage temp.

2-8°C

SMILES string

NC(N)=O

InChI

1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)

InChI key

XSQUKJJJFZCRTK-UHFFFAOYSA-N

Gene Information

human ... CA1(759), CA2(760), EPHX2(2053)
mouse ... Ephx2(13850)
rat ... Ppm1a(24666)

Application

Recommended for the detection of urease activity.

Biochem/physiol Actions

Urea solution is primarily used for protein denaturation. It also increases solubility of hydrocarbons and reduce micelle formation. Urea solution at high concentration leads to the destabilization of amyloid β16−22 oligomers.

Preparation Note

Warm the refrigerated 40% urea solution to room temperature. Aseptically add 5 mL to 95 mL of sterile molten Urea Agar Base (Christensen). Mix well and dispense in sterile tubes.


Still not finding the right product?

Explore all of our products under Urea solution


Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Regulatory Information

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library


Related Content


Aqueous urea solutions: structure, energetics, and urea aggregation
Stumpe MC, et al.
The Journal of Physical Chemistry B, 111(22), 6220-6228 (2007)
G L French et al.
Lancet (London, England), 2(8551), 117-119 (1987-07-18)
Tuberculostearic acid, a structural component of Mycobacterium tuberculosis, was identified by gas chromatography/mass spectrometry with selected ion monitoring in cerebrospinal fluid (CSF) from 13 patients with proven and 8 out of 9 patients with suspected tuberculous meningitis; the negative result
Annette Bahlinger et al.
Angewandte Chemie (International ed. in English), 53(33), 8779-8783 (2014-03-20)
β-Amino thioesters are important natural building blocks for the synthesis of numerous bioactive molecules. An organocatalyzed Mannich reaction was developed which provides direct and highly stereoselective access to acyclic β(2)- and β(2,3,3)-amino thioesters with adjacent tertiary and quaternary stereocenters. Mechanistic



Global Trade Item Number

SKUGTIN
U7129-1VL04061837410093