V800191
甲酸
AR, ≥90%
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线性分子式:
HCOOH
化学文摘社编号:
分子量:
46.03
UNSPSC Code:
12352106
EC Number:
200-579-1
PubChem Substance ID:
Beilstein/REAXYS Number:
1209246
MDL number:
Assay:
≥90%
Grade:
AR
InChI key
BDAGIHXWWSANSR-UHFFFAOYSA-N
InChI
1S/CH2O2/c2-1-3/h1H,(H,2,3)
SMILES string
OC=O
grade
AR
vapor density
1.6 (vs air)
vapor pressure
44.8 mmHg ( 20 °C)
product line
Vetec™
assay
≥90%
autoignition temp.
1004 °F
expl. lim.
57 %
refractive index
n20/D 1.370 (lit.)
bp
100-101 °C (lit.)
mp
8.2-8.4 °C (lit.)
density
1.22 g/mL at 25 °C (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
121.1 °F - closed cup
flash_point_c
49.5 °C - closed cup
法规信息
新产品
此项目有
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Protein S-nitrosylation, a post-translational modification (PTM) consisting of the covalent binding of nitric oxide (NO) to a cysteine thiol moiety, plays a major role in cell signaling and is recognized to be involved in numerous physiological processes and diseases in
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Oncotarget, 6(34), 35173-35182 (2015-10-16)
Inner centromere protein (INCENP) is a part of a protein complex known as the chromosomal passenger complex (CPC) that is essential for correcting non-bipolar chromosome attachments and for cytokinesis. We here demonstrate that a protein arginine methyltransferase PRMT1, which are
Stephan Kolodziej et al.
Nature communications, 5, 3995-3995 (2014-05-31)
The transcription factor Tal1 is a critical activator or repressor of gene expression in hematopoiesis and leukaemia. The mechanism by which Tal1 differentially influences transcription of distinct genes is not fully understood. Here we show that Tal1 interacts with the
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PLoS genetics, 11(10), e1005554-e1005554 (2015-10-07)
Studying the complex relationship between transcription, translation and protein degradation is essential to our understanding of biological processes in health and disease. The limited correlations observed between mRNA and protein abundance suggest pervasive regulation of post-transcriptional steps and support the
Matthew J Crisp et al.
The Journal of clinical investigation, 125(7), 2772-2780 (2015-06-16)
Therapeutic strategies that target disease-associated transcripts are being developed for a variety of neurodegenerative syndromes. Protein levels change as a function of their half-life, a property that critically influences the timing and application of therapeutics. In addition, both protein kinetics
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