1006-02-6

Basic information

• Product Name: 1,3-DICHLOROPROPENE
• Synonyms: Cyclopentene, 1,3,3,4,5,5-hexafluoro-
• CAS NO: 1006-02-6
• Molecular Formula: C3H4Cl2
• Molecular Weight: 111
• Mol File: 1006-02-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-DICHLOROPROPENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-DICHLOROPROPENE(1006-02-6)
• EPA Substance Registry System: 1,3-DICHLOROPROPENE(1006-02-6)

Safety Data

• Hazardous Substances Data: 1006-02-6(Hazardous Substances Data)

Usage

General Description

1,3-Dichloropropene, also known as Telone or MCP, is a highly volatile and flammable chemical compound that is commonly used as a soil fumigant and pesticide. It is a colorless liquid with a sweet and pungent odor. 1,3-Dichloropropene is classified as a possible human carcinogen and poses significant risks to human health and the environment. Exposure to this chemical can cause irritation to the skin, eyes, and respiratory tract, as well as damage to the central nervous system. It is also toxic to aquatic organisms and has the potential to contaminate groundwater. Due to its hazardous nature, precautions must be taken when handling and using 1,3-Dichloropropene, and its use is heavily regulated in many countries.

Upstream product

• 3264-56-0 1H:3H-Hexafluorcyclopenten 
• 162148-90-5 4H,4H-hexafluorocyclopentene 
• 2344-15-2 1,2,3,3,4,5,5-heptafluorocyclopentene 
• 1007-85-8 1H,2H,4H/-Heptafluorcyclopentan 
• 1007-86-9 1H,2H/4H-Heptafluorcyclopentan 

Downstream Products

• 1005-74-9 2,3-dihydrohexafluorocyclopentene 
• 1005-73-8 (Z)-3,3,4,4,5,5-hexafluorocyclopent-1-ene 
• 3264-56-0 1H:3H-Hexafluorcyclopenten 
• 773-17-1 1H,3H-/Octafluorcyclopentan 

Related news

Replicated flux measurements of 1,3-DICHLOROPROPENE (cas 1006-02-6) emissions from a bare soil under field conditions07/25/2019

Field experiments offer the most acceptable approach to quantifying agricultural fumigant emissions but there is an absence of replicated field data in reported literature. Air concentration profiles of 1,3-dichloropropene (1,3-D) were determined on duplicate masts above the center of a treated ...detailed

Effect of fumigation with 1,3-DICHLOROPROPENE (cas 1006-02-6) on soil bacterial communities07/24/2019

1,3-Dichloropropene (1,3-D) is a potential candidate as a soil fumigant because of the restriction of methyl bromide (MB) in soil fumigation. So far, little is known about the bacteria diversity in 1,3-D fumigated soil. Therefore, the impact of 1,3-D on soil bacterial community was determined by...detailed

Modeling variation in 1,3-DICHLOROPROPENE (cas 1006-02-6) emissions due to soil conditions and applicator practices07/21/2019

The fumigant 1,3-dichloropropene (1,3-D) is widely used for control of soil-borne pests and pathogens, but post-application emissions may lead to off-site transport and possible human exposure. The fraction of applied material emitted into the atmosphere and the magnitude of peak emissions are t...detailed

Effects of fumigation with 1,3-DICHLOROPROPENE (cas 1006-02-6) on soil enzyme activities and microbial communities in continuous-cropping soil07/19/2019

The compound 1,3-D (1,3-dichloropropene) is a potential candidate soil fumigant due to the restrictions on methyl bromide (MB). To date, little is known about the soil microbial community changes induced by 1,3-D fumigation. Therefore, soil properties, related soil enzymes, genes encoding the ke...detailed

Simulating emissions of 1,3-DICHLOROPROPENE (cas 1006-02-6) after soil fumigation under field conditions07/18/2019

Soil fumigation is an important agricultural practice used to produce many vegetable and fruit crops. However, fumigating soil can lead to atmospheric emissions which can increase risks to human and environmental health. A complete understanding of the transport, fate, and emissions of fumigants...detailed

Sustainable alternatives to 1,3-DICHLOROPROPENE (cas 1006-02-6) for controlling root-knot nematodes and fungal pathogens in melon crops in Mediterranean soils: Efficacy and effects on soil quality07/17/2019

The control of agricultural pests is key to maintain economically viable crops. Increasing environmental awareness, however, is leading to more restrictive European policies regulating the use of certain pesticides due to their impact on human health and the soil system. Given this context, we e...detailed

Combined effect of a reduced dose of 1,3-DICHLOROPROPENE (cas 1006-02-6) and dimethyl disulfide on soilborne pests and tomato growth07/16/2019

The effects of 1,3-dichloropropene (1,3-D) plus dimethyl disulfide (DMDS) soil treatments on soilborne pests and tomato growth were evaluated in one laboratory study and two field trials. The laboratory study established that the combined effects were more efficient than the individual effects. ...detailed

Relevant articles and documents

Method for preparing halogenated pentacyclic olefin by gas-phase isomerization reaction

The invention relates to a method for preparing halogenated pentacyclic olefin by gas-phase isomerization reaction. The method comprises the following steps of: by adopting the halogenated pentacyclic olefin C5HxFyClz as a material, under the existence of an isomerization catalyst, generating the gas-phase isomerization reaction to obtain isomers of the halogenated pentacyclic olefin, wherein X is an integer from 0 to 2, Y is an integer from 4 to 7, Z is an integer from 0 to 4, the sum of X and Y and Z is 8, and the isomerization catalyst is prepared by adopting at least one of lithium fluoride, potassium fluoride, sodium fluoride, rubidium fluoride or cesium fluoride as an active component and loading the active component on at least one of carriers such as aluminium fluoride, magnesium fluoride, iron fluoride, chromium fluoride and zinc fluoride. The method has the advantages that the material is easy to obtain, the isomerization catalyst is low in price, the yield of the isomer is higher, and the method is applicable to large-scale preparation of the isomers of the halogenated pentacyclic olefin by gas-phase reaction.