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Merck

299367

Urea-12C

99.9 atom % 12C

Synonyme(s) :

Carbamide-12C

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About This Item

Formule linéaire :
H2N12CONH2
Numéro CAS:
57-13-6
Poids moléculaire :
60.04
UNSPSC Code:
12352111
PubChem Substance ID:
24858038
EC Number:
200-315-5
MDL number:
MFCD00198123

Nom du produit

Urea-12C, 99.9 atom % 12C

InChI key

XSQUKJJJFZCRTK-IGMARMGPSA-N

InChI

1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)/i1+0

SMILES string

N[12C](N)=O

description

13C-depleted

isotopic purity

99.9 atom % 12C

form

solid

mp

132-135 °C (lit.)

mass shift

depleted

Quality Level

200

Gene Information

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

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Catégories apparentées

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Classe de stockage

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (COA)

Lot/Batch Number
OI1397
04218HA
016F3752
02845DS

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Giora van Straten et al.
PloS one, 9(6), e100077-e100077 (2014-06-20)
The detoxification of ammonia occurs mainly through conversion of ammonia to urea in the liver via the urea cycle and glutamine synthesis. Congenital portosystemic shunts (CPSS) in dogs cause hyperammonemia eventually leading to hepatic encephalopathy. In this study, the gene
Julian Wampfler et al.
Journal of leukocyte biology, 98(3), 357-363 (2015-05-21)
Successful myeloid differentiation depends on the expression of a series of miRNAs. Thus, it is hardly surprising that miRNAs are globally repressed in AML, a disease mainly characterized by a block in cellular myeloid differentiation. Studies investigating the mechanisms for
Anne-Roos S Frenay et al.
PloS one, 10(6), e0129732-e0129732 (2015-06-11)
Some diseases associated with a temporary deterioration in kidney function and/or development of proteinuria show an apparently complete functional remission once the initiating trigger is removed. While it was earlier thought that a transient impairment of kidney function is harmless
Hannah M Kaneb et al.
Human molecular genetics, 24(5), 1363-1373 (2014-10-26)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the selective death of motor neurons. Causative mutations in the global RNA-processing proteins TDP-43 and FUS among others, as well as their aggregation in ALS patients, have identified defects
Jean-Ha Baek et al.
Human molecular genetics, 24(5), 1305-1321 (2014-10-26)
Hutchinson-Gilford progeria syndrome (HGPS) is a segmental progeroid syndrome with multiple features suggestive of premature accelerated aging. Accumulation of progerin is thought to underlie the pathophysiology of HGPS. However, despite ubiquitous expression of lamin A in all differentiated cells, the
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