| Identification | Back Directory | [Name]
[4-chloro-2-(hydroxymethyl)phenoxy]acetic acid | [CAS]
6386-63-6 | [Synonyms]
Trylone
Cloxyfoc
Clocxyfonac
4-Chloro-α-hydroxy-o-tolyloxyacetic acid
2-hydroxymethyl-4-chlorophenyloxyacetic acid
[2-(Hydroxymethyl)-4-chlorophenoxy]acetic acid
2-(4-Chloro-2-(hydroxyMethyl)phenoxy)acetic acid
Acetic acid, 2-[4-chloro-2-(hydroxymethyl)phenoxy]- | [EINECS(EC#)]
228-987-5 | [Molecular Formula]
C9H9ClO4 | [MDL Number]
MFCD01671830 | [MOL File]
6386-63-6.mol | [Molecular Weight]
216.62 |
| Chemical Properties | Back Directory | [Melting point ]
141 °C | [Boiling point ]
391.4±32.0 °C(Predicted) | [density ]
1.440±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
DMSO: 125 mg/mL (577.05 mM) | [form ]
neat | [pka]
3.07±0.10(Predicted) | [color ]
White to off-white | [BRN ]
2562257 | [Henry's Law Constant]
1.0×105 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) | [Major Application]
agriculture
environmental | [InChI]
1S/C9H9ClO4/c10-7-1-2-8(6(3-7)4-11)14-5-9(12)13/h1-3,11H,4-5H2,(H,12,13) | [InChIKey]
ZJRUTGDCLVIVRD-UHFFFAOYSA-N | [SMILES]
OCc1cc(Cl)ccc1OCC(O)=O |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,N | [Risk Statements ]
40-50 | [Safety Statements ]
36/37-61 | [RIDADR ]
UN 3077 9 / PGIII | [WGK Germany ]
3 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Aquatic Acute 1
Carc. 2 |
| Hazard Information | Back Directory | [Description]
Cloxyfonac is a herbicide usually formulated using the sodium salt. The acid is highly soluble in water and moderately volatile so there is some risk of drift. No information is available regarding its environmental persistence. It is moderately toxic to fish and aquatic invertebrates. Cloxyfonac has a low mammalian oral toxicity but may be a neurotoxicant. It is also a skin, eye and respiratory irritant. | [Uses]
Refer to the productμs Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support. | [Production Methods]
The commercial production of cloxyfonac involves the etherification of chloro-substituted phenols with glycolic acid derivatives, followed by chlorination and hydroxymethylation steps to yield the final phenoxyacetic acid structure. The synthesis is typically carried out under controlled temperature and pH conditions to ensure selectivity and yield. | [Mechanism of action]
Acts by modifying plant hormone activity | [Pesticide Type]
Herbicide; Plant Growth Regulator; Metabolite |
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| Company Name: |
SPIRO PHARMA
|
| Tel: |
|
| Website: |
www.spiropharma.com.cn |
| Company Name: |
BePharm Ltd
|
| Tel: |
400-685-9117 |
| Website: |
www.bepharm.com |
| Company Name: |
Musechem
|
| Tel: |
+1-800-259-7612 |
| Website: |
www.musechem.com |
|