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Chemical structure of CAS 632-22-4

Tetramethylurea

In Stock•Starting at $8 for 10 g•Purity ≥ 98%
CAS No.632-22-4
MDL No.MFCD00008319
MFC5H12N2O
MW116.16
InChI KeyAVQQQNCBBIEMEU-UHFFFAOYSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
10 g98%$8In Stock
25 g98%$8In Stock
4*25 g98%$26In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

1,1,3,3-tetramethylurea is a urea derivative substituted with methyl groups at the 1, 1, 3, and 3 positions. It is a metabolite observed in cancer metabolism and functions as a human metabolite.

CAS No.632-22-4
Product NameTetramethylurea
IrritantIrritant
Health HazardHealth Hazard
Signal Word:Danger
HCode:H302-H360-H361-H227
PCode:P203-P264-P270-P280-P301+P317-P318-P330-P405-P501-P210-P370+P378-P403

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Studies related to this compound and its mechanism of action

Volatile metabolites of higher plant crops as a photosynthesizing life support system component under temperature stress at different light intensities.

Advances in space research : the official journal of the Committee on Space Research (COSPAR) • Vol. 31, Issue 7 • 2003
PMID: 14503518DOI: 10.1016/s0273-1177(03)00121-2

Rheological study on lysozyme/tetramethylurea viscoelastic matrices.

Biophysical chemistry • Vol. 99, Issue 2 • 2002
PMID: 12377364DOI: 10.1016/s0301-4622(02)00142-4

Lysozyme viscoelastic matrices in tetramethylurea/water media: a small angle X-ray scattering study.

Biophysical chemistry • Vol. 99, Issue 2 • 2002
PMID: 12377367DOI: 10.1016/s0301-4622(02)00144-8

Characterization of the in vitro adhesion of Actinobacillus pleuropneumoniae to swine alveolar epithelial cells.

Veterinary microbiology • Vol. 88, Issue 1 • 2002
PMID: 12119138DOI: 10.1016/s0378-1135(02)00080-9

Documentation