trans-1,3-Dichloropropene (CAS 10061-02-6) — formula C3H4Cl2, molecular weight 110.97; category organic chemicals.
Documented applications: Uses: 1, 3-Dichloropropene is a mixture of cis and trans isomers used as a nematocide to fumigate soil before planting, [Reference #1], Farming (Pesticides) [Category: Industry], Used primarily in soil fumigants for nematodes or as component of soil fumigant mixtures, for nematodes, ., Breathing in contaminated air, drinking contaminated water, eating contaminated food, dermal and eye exposure (L893)., Formulations, Preparations: Mixture of equal quantities of (E)- and (Z)-isomers, 1, 3-Dichloropropene, 3-DICHLOROPROPENE TRANS-ISOMER, 45.9%, CIS-ISOMER, 41.6%, 2-DICHLOROPROPANE, 2.5%, TRICHLOROPROPENE ISOMER, 1.5%, EPICHLOROHYDRIN, 1.0%, OTHER IMPURITIES 7.5%, TELONE II, General Manufacturing Information: 1-Propene, 3-dichloro-, (1E)-: ACTIVE.
trans-1,3-Dichloropropene is a carbon-based organic compound with CAS registry number 10061-02-6 and molecular formula C3H4Cl2 (molecular weight 110.97), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 10061-02-6
Its molecular formula C3H4Cl2 comprises 3 C, 4 H, 2 Cl atoms.
Also known as: trans-1,3-Dichloropropene · E-1,3-Dichloropropene
Category: organic chemicals
The CAS registry number of trans-1,3-Dichloropropene is 10061-02-6.
Molecular formula C3H4Cl2, molecular weight 110.97.
It is also registered under: trans-1,3-Dichloropropene, E-1,3-Dichloropropene.
Recorded applications: Uses: 1, 3-Dichloropropene is a mixture of cis and trans isomers used as a nematocide to fumigate soil before planting, [Reference #1], Farming (Pesticides) [Category: Industry], Used primarily in soil fumigants for nematodes or as component of soil fumigant mixtures, for nematodes, ., Breathing in contaminated air, drinking contaminated water, eating contaminated food, dermal and eye exposure (L893)., Formulations, Preparations: Mixture of equal quantities of (E)- and (Z)-isomers, 1, 3-Dichloropropene, 3-DICHLOROPROPENE TRANS-ISOMER, 45.9%, CIS-ISOMER, 41.6%, 2-DICHLOROPROPANE, 2.5%, TRICHLOROPROPENE ISOMER, 1.5%, EPICHLOROHYDRIN, 1.0%, OTHER IMPURITIES 7.5%, TELONE II, General Manufacturing Information: 1-Propene, 3-dichloro-, (1E)-: ACTIVE.
Category: Organic Chemicals.
Public-database records for trans-1,3-Dichloropropene (CAS 10061-02-6), reproduced here for independent cross-checking.
| GHS notification summary | 4.8% (1 / 21) |
|---|---|
| Reported hazard statements | H226 (28.6%), H301 (14.3%), H302 (81%), H311 (14.3%), H315 (14.3%), H317 (14.3%), H319 (19%), H351 (81%) |
This chemical does not meet GHS hazard criteria for 4.8% (1 of 21) of reports.
H226 (28.6%): Flammable liquid and vapor [Warning Flammable liquids]
| GHS notification summary | 4.8% (1 / 21) |
|---|
| 沸点 | 234 °F at 760 mmHg (NTP, 1992) |
|---|---|
| 沸点 | 112 °C |
| 沸点 | 112.00 °C. @ 760.00 mm Hg |
| 熔点 | -50 °C |
| 溶解度 | In water, 2,800 mg/l @ 25 °C. |
| 溶解度 | 2800 mg/L @ 20 °C (exp) |
| 密度 | 1.224 @ 20 °C/4 °C |
| Vapor 密度 | 1.4 AT 37.8 °C (AIR= 1) |
| 蒸气压 | 34 mmHg at 77 °F (NTP, 1992) |
| 蒸气压 | 34.0 [mmHg] |
| CAS Registry Number | 10061-02-6 |
|---|---|
| PubChem CID | 24726 |
| 分子式 | C3H4Cl2 |
| IUPAC 名称 | (E)-1,3-dichloroprop-1-ene |
| UNII(FDA) | 21UG87ODPI |
trans-1,3-Dichloropropene; 10061-02-6; 1-Propene, 1,3-dichloro-, (1E)-; trans-1,3-Dichloropropylene; (1E)-1,3-dichloroprop-1-ene; (E)-1,3-Dichloropropene; (E)-1,3-Dichloro-1-propene; trans-Telone; trans-1,3-Dichloro-1-propene; trans-3-Chloroallyl chloride; 1,3-Dichloropropene, trans-; E-1,3-Dichloropropene; 1-Propene, 1,3-dichloro-, (E)-; (1E)-1,3-dichloro-1-propene; Propene, 1,3-dichloro-, (E)-; 21UG87ODPI
| 分子量 | 110.97 |
|---|---|
| XLogP3 | 1.7 |
| 氢键供体数 | 0 |
| 氢键受体数 | 0 |
| 可旋转键数 | 1 |
| 精确质量 | 109.9690055 |
| 单同位素质量 | 109.9690055 |
| 拓扑极性表面积 | 0 |
| 重原子数 | 5 |
| 形式电荷 | 0 |
trans-1,3-Dichloropropene · CAS 10061-02-6 · C3H4Cl2. UNII 21UG87ODPI. 沸点: 234 °F at 760 mmHg (NTP, 1992); 沸点: 112 °C; 沸点: 112.00 °C. @ 760.00 mm Hg.
Source: PubChem / Wikidata; the batch COA governs where values differ.
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