CAS Number101-21-3
SynonymsChlorpropham; chlor-IPC; 1-methylethyl (3-chlorophenyl)carbamate; MFCD00037108; isopropyl 3-chlorocarbanilate; Carbamic acid, N-(3-chlorophenyl)-, 1-methylethyl ester; propan-2-yl (3-chlorophenyl)carbamate; propan-2-yl N-(3-chlorophenyl)carbamate; EINECS 202-925-7; Isopropyl m-chlorocarbanilate; Bud Nip; Taterpex; Isopropyl (3-chlorophenyl)carbamate; 1-methylethyl N-(3-chlorophenyl)carbamate
Molecular FormulaC10H12NO2Cl
Molecular Weight213.66
Purity98.00%
Density1.2±0.1 g/cm3
Boiling Point251.1±23.0 °C at 760 mmHg
Melting Point41°C
AppearanceBeige to brown solid
EINECS202-925-7
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 101-21-3 |
| Catalog No. | 2A-9018246 |
| Chinese Name | 氯苯胺灵 |
| Synonyms | Chlorpropham; chlor-IPC; 1-methylethyl (3-chlorophenyl)carbamate; MFCD00037108; isopropyl 3-chlorocarbanilate; Carbamic acid, N-(3-chlorophenyl)-, 1-methylethyl ester; propan-2-yl (3-chlorophenyl)carbamate; propan-2-yl N-(3-chlorophenyl)carbamate; EINECS 202-925-7; Isopropyl m-chlorocarbanilate; Bud Nip; Taterpex; Isopropyl (3-chlorophenyl)carbamate; 1-methylethyl N-(3-chlorophenyl)carbamate |
| Molecular Formula | C10H12NO2Cl |
| Molecular Weight | 213.66 |
| Purity | 98.00 |
| Density | 1.2±0.1 g/cm3 |
| Boiling Point | 251.1±23.0 °C at 760 mmHg |
| Melting Point | 41°C |
| Appearance | Beige to brown solid |
| Water Solubility | 0.009 g/100 ml very poor |
| Storage Condition | Store in a cool, ventilated warehouse. Keep away f |
| Packaging | I; II; III |
| Application | Chloropropylamine is a carbamate herbicide and plant growth regulator. Chloropropylamine inhibits mitosis and cell division by interfering with the organization of spindle microtubules [1][2]. |
| EINECS | 202-925-7 |
| HTC | 2924299035 |
| UN(IATA) | UN 无资料 |
| PubChem ID | 329756697 |
| MDL Number | MFCD00037108 |
| SMILES | CC(C)OC(=O)Nc1cccc(Cl)c1 |
| InChI | 1S/C10H12ClNO2/c1-7(2)14-10(13)12-9-5-3-4-8(11)6-9/h3-7H,1-2H3,(H,12,13) |
| InChI Key | CWJSHJJYOPWUGX-UHFFFAOYSA-N |
| Beilstein/REAXYS | 2211397 |
| NACRES Code | NA.24 |
| UNSPSC | 41116107 |
| Hazard Symbols | 6.1 |
| MSDS | msds/18246_1_101_21_3.pdf |
| Bioactivity | Chlorpropham is a carbamate herbicide and plant growth regulator. Chlorpropham inhibits mitosis and cell division by interfering with the organisation of the spindle microtubules[1][2]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Chlorpropham (1-20 μM; 6 d) inhibits cell division of D. salina cultures[2]. Chlorpropham (10 or 20 μM; 6 d) shows increasement of phytoene in D. salina cultures under red LED light[2]. Chemical & Physical Properties Density 1.2±0.1 g/cm3 Boiling Point 251.1±23.0 °C at 760 mmHg Melting Point 41°C Molecular Formula C10H12ClNO2 Molecular Weight 213.661 Flash Point 105.7±22.6 °C Exact Mass 213.055649 PSA 38.33000 LogP 3.49 Vapour Pressure 0.0±0.5 mmHg at 25°C Index of Refraction 1.561 InChIKey CWJSHJJYOPWUGX-UHFFFAOYSA-N SMILES CC(C)OC(=O)Nc1cccc(Cl)c1 Water Solubility 0.009 g/100 ml very poor |
| Use of | Chlorpropham is a carbamate herbicide and plant growth regulator. Chlorpropham inhibits mitosis and cell division by interfering with the organisation of the spindle microtubules[1][2]. Properties Articles27 Name chlorpropham Synonym More Synonyms Chlorpropham Biological Activity Description Chlorpropham is a carbamate herbicide and plant growth regulator. Chlorpropham inhibits mitosis and cell division by interfering with the organisation of the spindle microtubules[1][2]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Chlorpropham (1-20 μM; 6 d) inhibits cell division of D. salina cultures[2]. Chlorpropham (10 or 20 μM; 6 d) shows increasement of phytoene in D. salina cultures under red LED light[2]. Chemical & Physical Properties Exact Mass 213.055649 PSA 38.33000 Index of Refraction 1.561 InChIKey CWJSHJJYOPWUGX-UHFFFAOYSA-N |
| Tax Rebate | 9.0% |
| Supervision | S. Import and export pesticide registration certificate |
| Transport Info | Product name: Chemical name |
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