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trans-1,3-Dichloropropene - 97%, high purity , CAS No.10061-02-6

3 Citations COA COA
    Grade & Purity:
  • ≥97%
In stock
Item Number
D115814
Grouped product items
SKU Size
Availability
 Price Qty
D115814-5ml
5ml
2
$125.90
D115814-25ml
25ml
3
$410.90
D115814-100ml
100ml
2
$1,477.90
D115814-500ml
500ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$6,648.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Halogenated alkene (35) Non heterocyclic block (8163)

Basic Description

Synonyms alpha,gamma-Dichloropropylene | Propene, 1,3-dichloro-, (E)- | Vorlex 201 | CAS-542-75-6 | Dedisol C | gamma-chloroallylchloride | 1,3-Dichloropropene, trans- | HSDB 1109 | 1-Propene, 1,3-dichloro- | 3-Chloropropenyl chloride | DTXCID501307 | Propene, 1,3
Specifications & Purity ≥97%
Storage Temp Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organohalogen compounds
Class Vinyl halides
Subclass Vinyl chlorides
Intermediate Tree Nodes Not available
Direct Parent Vinyl chlorides
Alternative Parents Chloroalkenes  Organochlorides  Hydrocarbon derivatives  Alkyl chlorides  
Molecular Framework Aliphatic acyclic compounds
Substituents Chloroalkene - Haloalkene - Vinyl chloride - Hydrocarbon derivative - Organochloride - Alkyl halide - Alkyl chloride - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as vinyl chlorides. These are vinyl halides in which a chlorine atom is bonded to an sp2-hybridised carbon atom.
External Descriptors Nematicides

Associated Targets(Human)

NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Aspergillus nidulans (364 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ralstonia solanacearum (520 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Salmonella typhimurium (15756 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Meloidogyne incognita (862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Botrytis cinerea (4183 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cucumis sativus (803 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Digitaria sanguinalis (1594 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Solanum lycopersicum (493 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Stellaria media (151 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Arenaria serpyllifolia (16 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Capsella bursa-pastoris (46 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Phytophthora melonis (2 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504753252
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504753252
IUPAC Name (E)-1,3-dichloroprop-1-ene
INCHI InChI=1S/C3H4Cl2/c4-2-1-3-5/h1-2H,3H2/b2-1+
InChIKey UOORRWUZONOOLO-OWOJBTEDSA-N
Smiles C(C=CCl)Cl
Isomeric SMILES C(/C=C/Cl)Cl
WGK Germany 3
RTECS UC8320000
UN Number 2047
Packing Group II
Molecular Weight 110.97
Beilstein 1(4)743
Reaxy-Rn 1719556
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1719556&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot Number Certificate Type Date Item
E2407061 Certificate of Analysis Aug 04, 2023 D115814
K2115049 Certificate of Analysis Aug 04, 2023 D115814
K2115047 Certificate of Analysis Aug 04, 2023 D115814
K2115048 Certificate of Analysis Aug 04, 2023 D115814
K2115050 Certificate of Analysis Aug 04, 2023 D115814

Chemical and Physical Properties

Solubility Solubility in water: Practically insoluble; Soluble in Chloroform,Ether,Benzene
Sensitivity Air & heat Sensitive
Refractive Index 1.47
Flash Point(°F) 11 °C
Flash Point(°C) 11°C
Boil Point(°C) 112°C
Molecular Weight 110.970 g/mol
XLogP3 1.700
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 1
Exact Mass 109.969 Da
Monoisotopic Mass 109.969 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 5
Formal Charge 0
Complexity 31.900
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 1
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 1
Covalently-Bonded Unit Count 1

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Qiaochu Zhang, Meiling Qi, Jinliang Wang.  (2017)  Star-shaped oligothiophene-functionalized truxene materials as stationary phases for capillary gas chromatography.  JOURNAL OF CHROMATOGRAPHY A,  1525  (152). 
2. Xiaohong Yang, Changxia Li, Meiling Qi, Liangti Qu.  (2016)  Graphene-ZIF8 composite material as stationary phase for high-resolution gas chromatographic separations of aliphatic and aromatic isomers.  JOURNAL OF CHROMATOGRAPHY A,  1460  (173). 
3. Chunyun Gu, Jiayi An, Shuyu Liu, Feng Xiong, Wei Zhou, Liting Tian, Yuruo Wan, Qian Wu, Jie Ma.  (2025)  Degradation of 15 halogenated hydrocarbons by 5 unactivated in-situ chemical oxidation oxidants.  ENVIRONMENTAL TECHNOLOGY,     

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