4-Methylumbelliferyl-N-acetyl-ß-D-glucosaminide
Suppliers
Names
[ CAS No. ]:
37067-30-4
[ Name ]:
4-Methylumbelliferyl-N-acetyl-ß-D-glucosaminide
[Synonym ]:
4-Methyl-2-oxo-2H-chromen-7-yl 2-acetamido-2-deoxy-β-D-glucopyranoside
4-Methylumbelliferyl 2-Acetamido-2-deoxy-β-D-glucopyranoside
GLCNAC1-B-4MU
MFCD00065481
4-Methylumbelliferyl-N-acetyl-ß-D-glucosaminide
4-Methylumbelliferyl-N-acetyl-β-D-glucosaminide
7-((2-Acetamido-2-deoxy-β-D-glucopyranosyl)oxy)-4-methyl-2H-1-benzopyran-2-one
EINECS 253-333-0
Methylumbelliferyl-N-acetyl-b-D-glucosaminide
2H-1-Benzopyran-2-one, 7-[[2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]oxy]-4-methyl-
T66 BOVJ E1 IO- BT6OTJ CMV1 DQ EQ F1Q &&β-D-Gluco Form
Chemical & Physical Properties
[ Density]:
1.5±0.1 g/cm3
[ Boiling Point ]:
732.2±60.0 °C at 760 mmHg
[ Melting Point ]:
208-210 °C
[ Molecular Formula ]:
C18H21NO8
[ Molecular Weight ]:
379.361
[ Flash Point ]:
396.6±32.9 °C
[ Exact Mass ]:
379.126709
[ PSA ]:
138.46000
[ LogP ]:
0.34
[ Vapour Pressure ]:
0.0±2.5 mmHg at 25°C
[ Index of Refraction ]:
1.632
[ Storage condition ]:
−20°C
[ Stability ]:
Light Sensitive - Protect from Light
[ Water Solubility ]:
DMF: 20 mg/mL, clear, colorless
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xn
[ Safety Phrases ]:
S22-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Articles
J. Med. Genet. 28(2) , 101-9, (1991)
An assay for measuring hexosaminidase A in serum and leucocytes is described in which a centrifugal analyser is used for automation of the enzyme assays after manual heat inactivation. The assay was u...
Apoptosis 14(3) , 320-32, (2009)
Macrophages are the principal source of TNFalpha, yet they are highly resistant to TNFalpha-mediated cell death. Previously, employing in vitro differentiated human macrophages, we showed that followi...
Electrophoresis 15(5) , 662-5, (1994)
A method for the detection of N-acetylglucosaminidase (GlcNAcase) activity has been developed by using 4-methyl-umbelliferyl-N-acetyl-D-glucosaminide (4-MU-GlcNAc) as substrate in crossed immunoelectr...