All Photos(1)
Synonym(s):
Chlormequat chloride, Chlorocholine chloride, Choline dichloride
Linear Formula:
(CH3)3N(Cl)CH2CH2Cl
CAS Number:
Molecular Weight:
158.07
Beilstein:
3563994
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
98%
form
solid
mp
239-243 °C (dec.) (lit.)
SMILES string
[Cl-].C[N+](C)(C)CCCl
InChI
1S/C5H13ClN.ClH/c1-7(2,3)5-4-6;/h4-5H2,1-3H3;1H/q+1;/p-1
InChI key
UHZZMRAGKVHANO-UHFFFAOYSA-M
Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
农药列管产品
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M E Poulsen et al.
Analytical and bioanalytical chemistry, 389(6), 1799-1804 (2007-09-13)
Chlormequat is a plant growth regulator widely used on cereals, and there is general concern that it may impair human fertility. A LC-MS/MS method for the analysis of chlormequat in milk and serum was developed and validated in connection with
René K Juhler et al.
Environmental science and pollution research international, 17(6), 1245-1256 (2010-02-24)
Chlormequat (Cq) is a plant growth regulator used throughout the world. Despite indications of possible effects of Cq on mammalian health and fertility, little is known about its fate and transport in subsurface environments. The aim of this study was
Hua Cheng et al.
Plant cell reports, 30(1), 49-62 (2010-11-04)
Chalcone isomerase (CHI, EC 5.5.1.6) is one of the key enzymes in the flavonoid biosynthesis pathway catalyzing the stereospecific isomerization of chalcones into their corresponding (2S)-flavanones. In this investigation, both the cDNA sequence and the genomic sequence encoding the chalcone
Oscar Núñez et al.
Journal of mass spectrometry : JMS, 39(8), 873-883 (2004-08-27)
Fragmentation studies using both an ion-trap mass analyzer and a hybrid quadrupole time-of-flight (Q-TOF) mass spectrometer were performed in order to establish the fragmentation pathways of organic molecules. A general strategy combining MSn data (n = 1-4) in an ion-trap
Xing-li Guo et al.
Ecotoxicology and environmental safety, 73(4), 642-646 (2010-01-12)
A simple and reliable analytical method for chlormequat residues in cotton and soil was established in this study. The residual levels and dissipation rates of chlormequat in cotton crops and soil were determined by High Performance Liquid Chromatography-Mass Spectroscopy (HPLC-MS).
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