JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Chemistry & Biochemicals
Building Blocks
Organic Building Blocks
1,12-Dibromododecane - 95%, high purity , CAS No.3344-70-5

Skip to the end of the images gallery

Skip to the beginning of the images gallery

1,12-Dibromododecane - 95%, high purity , CAS No.3344-70-5

15 Citations

COA

Grade & Purity:

≥95%

Cas Number: 3344-70-5
Molecular Weight: 328.13
Beilstein Registry Number: 1742763
EC Number: 222-096-5
MDL number: MFCD00000226
PubChem CID: 18766

In stock

Item Number

D670404

Grouped product items
SKU	Size	Availability	Price
D670404-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$12.90
D670404-25g	25g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$45.90
D670404-100g	100g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$149.90

View related series

Halogenated alkene (35) Non heterocyclic block (8163)

Basic Description

Synonyms	Dodecamethylene dibromide
Specifications & Purity	≥95%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	1,12-Dibromododecane was used for the preparation of tboc-protected ionenes.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organohalogen compounds
  - Class Organobromides

Kingdom	Organic compounds
Superclass	Organohalogen compounds
Class	Organobromides
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Organobromides
Alternative Parents	Hydrocarbon derivatives Alkyl bromides
Molecular Framework	Aliphatic acyclic compounds
Substituents	Hydrocarbon derivative - Organobromide - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as organobromides. These are compounds containing a chemical bond between a carbon atom and a bromine atom.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	1,12-dibromododecane
INCHI	InChI=1S/C12H24Br2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-12H2
InChIKey	ZJJATABWMGVVRZ-UHFFFAOYSA-N
Smiles	C(CCCCCCBr)CCCCCBr
Isomeric SMILES	C(CCCCCCBr)CCCCCBr
WGK Germany	3
RTECS	JR2295000
Molecular Weight	328.13
Beilstein	1742763
Reaxy-Rn	1742763
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1742763&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.

4 results found

Lot Number	Certificate Type	Date	Item
H2406409	Certificate of Analysis	Aug 14, 2024	D670404
H2406410	Certificate of Analysis	Aug 14, 2024	D670404
H2406407	Certificate of Analysis	Aug 14, 2024	D670404
H2406408	Certificate of Analysis	Aug 14, 2024	D670404

Chemical and Physical Properties

Flash Point(°F)	235.4 °F
Flash Point(°C)	113 °C
Boil Point(°C)	215 °C/15 mmHg
Melt Point(°C)	38-42°C
Molecular Weight	328.130 g/mol
XLogP3	6.900
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	11
Exact Mass	328.022 Da
Monoisotopic Mass	326.024 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	14
Formal Charge	0
Complexity	82.300
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Haihua Wang, Guangyu Hu, Xuan Liu, Liyuan Guo, Xiaorui Li, Ruiyuan Guo, Yanyu Li. (2022) Concurrent alkylation and crosslinking of polyaniline for enhanced anticorrosive performance of waterborne alkyd coating. PROGRESS IN ORGANIC COATINGS, 168 (106865).
2. Jiefeng Pan, Yanyao Tao, Lei Zhao, Xiaohong Yu, Xueting Zhao, Tao Wu, Lifen Liu. (2021) Green preparation of quaternized vinylimidazole-based anion exchange membrane by photopolymerization. SEPARATION AND PURIFICATION TECHNOLOGY, 276 (119220).
3. Guangliang Hou, Shenxi Min, Yuhan Zhao, Bin Dong, Lina Zhang, Dahua Li, Weichun Wu, Huifang Zhu, Bo Song. (2020) Emission shift of an amphiphilic α-cyanostilbene derivative through concentration-driven two-step assembly with cucurbit[7]uril. DYES AND PIGMENTS, 180 (108460).
4. Junjun Wang, Xiaojiao Zhu, Jie Zhang, Haiyan Wang, Gang Liu, Yingcui Bu, Jianhua Yu, Yupeng Tian, Hongping Zhou. (2020) AIE-Based Theranostic Agent: In Situ Tracking Mitophagy Prior to Late Apoptosis To Guide the Photodynamic Therapy. ACS Applied Materials & Interfaces, 12 (2): (1988–1996).
5. Lunqiang Jin, Zhenqiang Shi, Xiang Zhang, Xiaoling Liu, Huiling Li, Jingxia Wang, Feng Liang, Weifeng Zhao, Changsheng Zhao. (2019) Intelligent antibacterial surface based on ionic liquid molecular brushes for bacterial killing and release. Journal of Materials Chemistry B, 7 (36): (5520-5527).
6. Jie Li, Yong Kang, Bohao Li, Xin Wang, Dan Li. (2018) PEG-Linked Functionalized Dicationic Ionic Liquids for Highly Efficient SO2 Capture through Physical Absorption. ENERGY & FUELS, 32 (12): (12703–12710).
7. Fangxia Yang, Junhua Zhang, Yingjie Guo, Lele Feng, Shijun Wei, Shuai Chen. (2018) Producing Fatty Acid Methyl Esters from Free Fatty Acids with Ionic Liquids as Catalyst. CHEMICAL ENGINEERING & TECHNOLOGY, 42 (1): (174-181).
8. Chen Fan, Hongqiang Dong, You Liang, Jiale Yang, Gang Tang, Wenbing Zhang, Yongsong Cao. (2019) Sustainable synthesis of HKUST-1 and its composite by biocompatible ionic liquid for enhancing visible-light photocatalytic performance. Journal of Cleaner Production, 208 (353).
9. Cuihong Jin, Xiuling Zhu, Shuai Zhang, Shuai Li. (2018) Highly conductive flexible alkylsulfonated side chains poly(phthalazinone ether ketone)s for proton exchange membranes. POLYMER, 148 (269).
10. Jing Zhang, Jingjiang Liu, Yong Zuo, Rongmin Wang, Yubing Xiong. (2015) Preparation of Thermo-Responsive Poly(ionic liquid)s-Based Nanogels via One-Step Cross-Linking Copolymerization. MOLECULES, 20 (9): (17378-17392).
11. Yuanji Gao, Bing Xia, Jie Liu, Lisheng Ding, Bangjing Li, Yan Zhou. (2015) Reversible tuning of the wettability on a silver mesodendritic surface by the formation and disruption of lipid-like bilayers. APPLIED SURFACE SCIENCE, 329 (150).
12. Yanhui Hu, Hua Yue, Shiqi Huang, Bingxi Song, Yuyuan Xing, Minmin Liu, Gongying Wang, Yanyan Diao, Suojiang Zhang. (2024) Biocompatible diimidazolium based ionic liquid systems for enhancing the solubility of paclitaxel. GREEN CHEMISTRY,
13. Dong Chenshan, Yao Yiting, Li Sanchuan, Ma Dongdong, Zhang Ruquan, Liu Xin, Shang Bin, Huang Jingjing, Gu Shaojin, Du Jiehao. (2024) Designing multifunctional cotton fabrics based on dipentaerythritol pentaacrylate-branched poly(ethyleneimine) (5Acl-BPEI) reactive coating. CELLULOSE, 31 (6): (3947-3960).
14. Jin Dangqin, Zhou Hui, Xiao Jiali, Gao Qin, Gong Aiqin. (2025) Sensitive determination of organophosphorus pesticide residues in fruits and vegetables by solid phase extraction and enzyme inhibition UV-spectrophotometry. SPECTROSCOPY LETTERS,
15. Xinxin Fu, Dongling Cai, Yingying Zhang, Fangdong Ning, Xianmei Ma, Ying Luo, Wei Li, Lei Zou, Yongjun Zhang. (2024) Versatile Regioselective Friedel–Crafts Hydroxyalkylation Polycondensation toward Linear Polymers Containing Triphenylmethane Backbone Structures. ACS Applied Polymer Materials, 6 (23): (14619-14628).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.