A1799
Acrylamide
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About This Item
EC Number:
UNSPSC Code:
12352200
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Carc. 1B - Eye Irrit. 2 - Muta. 1B - Repr. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 1 Oral
Target Organs
Peripheral nervous system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
280.4 °F - closed cup
Flash Point(C)
138 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Effect of dose volume on the toxicokinetics of acrylamide and its metabolites and 2-deoxy-D-glucose.
Burhan I Ghanayem et al.
Drug metabolism and disposition: the biological fate of chemicals, 37(2), 259-263 (2008-11-22)
Acrylamide (AA) is a known mutagen and animal carcinogen. Comparison of recent studies revealed significant quantitative differences in AA-induced germ cell mutagenicity. It was hypothesized that despite the administration of AA at similar doses, the discrepancy in the observed effects
Thien Nguyen et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 29(3), 630-637 (2009-01-23)
Progressive axonal degeneration follows demyelination in many neurological diseases, including multiple sclerosis and inherited demyelinating neuropathies, such as Charcot-Marie-Tooth disease. One glial molecule, the myelin-associated glycoprotein (MAG), located in the adaxonal plasmalemma of myelin-producing cells, is known to signal to
Brent Sullenbarger et al.
Experimental hematology, 37(1), 101-110 (2008-11-18)
Methods producing human platelets using growth on plastic, on feeder layers, or in suspension have been described. We hypothesized that growth of hematopoietic progenitors in a three-dimensional (3D) scaffold would enhance platelet production sans feeder layer. We grew CD34 positively
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