CAS 37764-25-3|Dichlormid
| Common Name | Dichlormid | ||
|---|---|---|---|
| CAS Number | 37764-25-3 | Molecular Weight | 208.085 |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 253.8±40.0 °C at 760 mmHg |
| Molecular Formula | C8H11Cl2NO | Melting Point | 5.0-6.5°C |
| MSDS | USA | Flash Point | 107.3±27.3 °C |
| Symbol | GHS07 | Signal Word | Warning |
Names
| Name | dichlormid |
|---|---|
| Synonym | More Synonyms |
Dichlormid BiologicalActivity
| Description | Dichlormid is a herbicide safener. Dichlormid up-regulates expression of ZmGST27 and ZmMRP1 and increases ZmGT1[1][2]. |
|---|---|
| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
| References | [1]. D P Dixon, et al. Purification, Regulation and Cloning of a Glutathione Transferase (GST) From Maize Resembling the Auxin-Inducible type-III GSTs. Plant Mol Biol. 1998 Jan;36(1):75-87. [2]. Sen Pang, et al. Co-induction of a glutathione-S-transferase, a Glutathione Transporter and an ABC Transporter in Maize by Xenobiotics. PLoS One. 2012;7(7):e40712. |
Chemical & Physical Properties
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 253.8±40.0 °C at 760 mmHg |
| Melting Point | 5.0-6.5°C |
| Molecular Formula | C8H11Cl2NO |
| Molecular Weight | 208.085 |
| Flash Point | 107.3±27.3 °C |
| Exact Mass | 207.021774 |
| PSA | 20.31000 |
| LogP | 1.98 |
| Vapour Pressure | 0.0±0.5 mmHg at 25°C |
| Index of Refraction | 1.495 |
| InChIKey | YRMLFORXOOIJDR-UHFFFAOYSA-N |
| SMILES | C=CCN(CC=C)C(=O)C(Cl)Cl |
| Storage condition | 0-6°C |
Toxicological Information
CHEMICAL IDENTIFICATION |
ACUTE TOXICITY DATA - TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Rodent - rat
- DOSE/DURATION :
- 2 gm/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- 85ARAE "Agricultural Chemicals," Thomson, W.T., 4 vols., Fresno, CA, Thomson Publications, 1976/77 revision Volume(issue)/page/year: 3,109,1976/1977
- TYPE OF TEST :
- LC50 - Lethal concentration, 50 percent kill
- ROUTE OF EXPOSURE :
- Inhalation
- SPECIES OBSERVED :
- Rodent - rat
- DOSE/DURATION :
- 5500 mg/m3/1H
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- PEMNDP Pesticide Manual. (The British Crop Protection Council, 20 Bridport Rd., Thornton Heath CR4 7QG, UK) V.1- 1968- Volume(issue)/page/year: 9,251,1991
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Administration onto the skin
- SPECIES OBSERVED :
- Rodent - rabbit
- DOSE/DURATION :
- >5 gm/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- PEMNDP Pesticide Manual. (The British Crop Protection Council, 20 Bridport Rd., Thornton Heath CR4 7QG, UK) V.1- 1968- Volume(issue)/page/year: 9,251,1991
Safety Information
| Symbol | GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302-H332 |
| Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
| Hazard Codes | Xi: Irritant;N: Dangerous for the environment; |
| Risk Phrases | R43;R50/53 |
| Safety Phrases | S45 |
| RIDADR | NONH for all modes of transport |
| RTECS | AB6080000 |
Articles8
More Articles| Fatty acid elongation is important in the activity of thiocarbamate herbicides and in safening by dichlormid. J. Exp. Bot. 54(385) , 1289-94, (2003) The thiocarbamates, such as pebulate (S-propyl butyl (ethyl) thiocarbamate) are a well-established class of herbicides. They inhibit fatty acid elongation, which is necessary for the biosynthesis of c... | |
| The inhibition of fatty acid elongation by pebulate can be effectively counteracted by the safener dichlormid. Biochem. Soc. Trans. 28(6) , 650-1, (2000) The thiocarbamate herbicide pebulate inhibits fatty acid elongation, which is necessary for surface lipid biosynthesis. As both barley and wild oats are susceptible to pebulate, the safener dichlormid... | |
| Induction of glutathione S-transferases in Arabidopsis by herbicide safeners. Plant Physiol. 130(3) , 1497-505, (2002) Herbicide safeners increase herbicide tolerance in cereals but not in dicotyledenous crops. The reason(s) for this difference in safening is unknown. However, safener-induced protection in cereals is ... |
Synonyms
| ACETAMIDE, 2,2-DICHLORO-N,N-DI-2-PROPENYL- |
| Acetamide, N,N-diallyl-2,2-dichloro- |
| 2,2-dichloro-N,N-di-2-propen-1-ylacetamide |
| N,N-Diallyldichloroacetamide |
| MFCD00072464 |
| N,N-diallyl-dichloroacetamide |
| N,N-Diallyldichloroacetamide,Dichloromid |
| Dichloromid |
| dichlorimid |
| Acetamide,2,2-dichloro-N,N-di-2-propenyl |
| Dichlormid |
| GYGVN2U1&2U1 |
| 2,2-dichloro-N,N-bis(prop-2-enyl)acetamide |
| Acetamide,N,N-diallyl-2,2-dichloro |
| 2,2-Dichloro-N,N-di(2-propèn-1-yl)acétamide |
| Acetamide, 2,2-dichloro-N,N-di-2-propen-1-yl- |
| Compound R-25788 |
| 2,2-dichloro-N,N-di(prop-2-en-1-yl)acetamide |
| 2,2-Dichloro-N,N-di-2-propenylacetamide |
| N,N-Diallyl-2,2-dichloroacetamide |
| N,N-Diallyl-2,3-dichloroacetamide |
| EINECS 253-658-8 |
| 2,2-Dichloro-N,N-diprop-2-en-1-ylacetamide |
| Stauffer R-25788 |
