| Company Name: |
TianJin Alta Scientific Co., Ltd.
|
| Tel: |
022-65378550-8551 |
| Email: |
contact@altascientific.com |
| Products Intro: |
Product Name:Alodane
CAS:2550-75-6
Purity:98% 10Mg 25Mg 100Mg
|
| Company Name: |
Alta Scientific Co., Ltd.
|
| Tel: |
022-6537-8550 15522853686 |
| Email: |
sales@altasci.com.cn |
| Products Intro: |
Product Name:Alodane
CAS:2550-75-6
Purity:99% Package:10mg,100mg
|
- Alodan
-
- $30.00
-
2026-05-11
- CAS:2550-75-6
- Purity: 99.75%
- Supply Ability: 10g
- Alodan
-
- $30.00
-
2026-05-11
- CAS:2550-75-6
- Purity: 99.75%
- Supply Ability: 10g
|
| Product Name: | ALODAN | | Synonyms: | 5,6-bis(chloromethyl)-1,2,3,4,7,7-hexachloro-2-norbornene;chlorbicyclen (bsi,iso);5,6-Bis(chloromethyl)-1,2,3,4,7,7-hexachloro-2-norbornene, Chlorbicyclene, Cyclodane;CHLORBICYCLEN;hercules12402;Nodon;1,2,3,4,7,7-hexachloro-5,6-bis(chloromethyl)-8,9,10-trinorborn-2-ene;ALODAN PESTANAL, 250 MG | | CAS: | 2550-75-6 | | MF: | C9H6Cl8 | | MW: | 397.77 | | EINECS: | | | Product Categories: | | | Mol File: | 2550-75-6.mol |  |
| | ALODAN Chemical Properties |
| Melting point | 104-106° | | Boiling point | bp2 172-176° | | density | 1.7593 (rough estimate) | | refractive index | 1.6000 (estimate) | | Fp | >100 °C | | storage temp. | -20°C Freezer | | solubility | DMSO (Sparingly), Methanol (Slightly) | | color | White to Off-White | | Merck | 13,2094 | | BRN | 2057350 | | EPA Substance Registry System | Chlorbicyclen (2550-75-6) |
| Hazard Codes | T+ | | Risk Statements | 21-25-26 | | Safety Statements | 28-36/37-45 | | RIDADR | 2761 | | WGK Germany | 3 | | RTECS | RB9470000 | | HazardClass | 6.1(b) | | PackingGroup | III | | Toxicity | LD50 orl-rat: 200 mg/kg JEENAI 61,743,68 |
| | ALODAN Usage And Synthesis |
| Description | Chlorbicyclen is an obsolete insecticide Little data is available regarding its environmental fate or ecotoxicology. It has a moderate oral mammalian toxicity. | | Uses | Chlorbicyclen (Alodan) is organic chloride insecticide[1]. | | Definition | ChEBI: Chlorbicyclen is an organochlorine compound. | | Production Methods | Chlorbicyclen, like other organochlorine insecticides of its era, would have been produced through stepwise chlorination and cyclisation reactions involving substituted bicyclic hydrocarbons, followed by controlled addition of chlorine across reactive double bonds to create the characteristic poly chlorinated bicyclic structure. Industrial production of organochlorines typically relied on chlorine gas or sulfuryl chloride, catalysts such as iron salts, and solvent systems that allowed heat controlled halogenation. After chlorination, the crude product would be purified by distillation or recrystallisation to yield technical grade chlorbicyclen for later formulation. | | Mechanism of action | Cyclodiene insecticides work by blocking gamma-aminobutyric acid (GABA)-gated chloride channels, leading to hyperexcitation of the nervous system in insects | | Safety Profile | A poison by ingestion.Moderately toxic by skin contact. When heated todecomposition it emits toxic vapors of Cl-. | | References | [1] Nthabiseng Motshabi, et al. Evaluation of organochlorine pesticide residues in Beta vulgaris, Brassica oleracea, and Solanum tuberosum in Bloemfontein markets, South Africa. Food Sci Nutr. 2021 Jul 29;9(9):4770-4779. DOI:10.1002/fsn3.2375 | | Pesticide Type | Insecticide; Acaricide |
| | ALODAN Preparation Products And Raw materials |
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