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2-Iodoethanol - ≥ 96.0% (GC), copper as stabilizer, high purity , CAS No.624-76-0

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2-Iodoethanol - ≥ 96.0% (GC), copper as stabilizer, high purity , CAS No.624-76-0

5 Citations

COA

Grade & Purity:

≥96%(GC)
copper as stabilizer

Cas Number: 624-76-0
Molecular Weight: 171.97
Beilstein Registry Number: 1339
PubChem CID: 12225
PubChem SID: 504752286

In stock

Item Number

I575056

Grouped product items
SKU	Size	Availability	Price
I575056-5g	5g	5	$23.90
I575056-25g	25g	5	$81.90
I575056-100g	100g	4	$230.90

Basic Description

Synonyms	2-IODOETHANOL \| 624-76-0 \| Ethanol, 2-iodo- \| Ethylene iodohydrin \| Iodoethanol \| 2-iodoethan-1-ol \| 2-iodo-ethanol \| MFCD00002830 \| EINECS 210-861-6 \| NSC 85227 \| BRN 1098258 \| AI3-61630 \| iodoethyl alcohol \| 2-Indoethanol \| 2-iodo-1-ethanol \| 2-iodoethyl alcohol \| 2 -iodoethyl alcohol
Specifications & Purity	≥96%(GC), copper as stabilizer
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice 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 Halohydrins
    - Subclass Iodohydrins

Kingdom	Organic compounds
Superclass	Organohalogen compounds
Class	Halohydrins
Subclass	Iodohydrins
Intermediate Tree Nodes	Not available
Direct Parent	Iodohydrins
Alternative Parents	Primary alcohols Organoiodides Hydrocarbon derivatives Alkyl iodides
Molecular Framework	Aliphatic acyclic compounds
Substituents	Iodohydrin - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organoiodide - Alkyl iodide - Alkyl halide - Alcohol - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as iodohydrins. These are alcohols substituted by a iodine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.
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

Pubchem Sid	504752286
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504752286
IUPAC Name	2-iodoethanol
INCHI	InChI=1S/C2H5IO/c3-1-2-4/h4H,1-2H2
InChIKey	QSECPQCFCWVBKM-UHFFFAOYSA-N
Smiles	C(CI)O
Isomeric SMILES	C(CI)O
WGK Germany	3
RTECS	KL3820000
Molecular Weight	171.97
Beilstein	1339
Reaxy-Rn	1098258
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098258&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.

7 results found

Lot Number	Certificate Type	Date	Item
C2328886	Certificate of Analysis	Apr 07, 2023	I575056
C2512034	Certificate of Analysis	Apr 07, 2023	I575056
C2328884	Certificate of Analysis	Apr 07, 2023	I575056
C2328883	Certificate of Analysis	Apr 07, 2023	I575056
C2328924	Certificate of Analysis	Apr 07, 2023	I575056
C2328875	Certificate of Analysis	Apr 07, 2023	I575056
C2328912	Certificate of Analysis	Apr 07, 2023	I575056

Chemical and Physical Properties

Solubility	Soluble in water.
Sensitivity	Sensitive to light; Sensitive to heat; Sensitive to air
Refractive Index	1.572
Flash Point(°F)	149 °F
Flash Point(°C)	65°C(lit.)
Boil Point(°C)	85 °C/25 mmHg
Molecular Weight	171.960 g/mol
XLogP3	0.600
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	171.939 Da
Monoisotopic Mass	171.939 Da
Topological Polar Surface Area	20.200 Å²
Heavy Atom Count	4
Formal Charge	0
Complexity	10.000
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. Jianxiong Xu, Yuecong Luo, Yin Chen, Ziyu Guo, Yutong Zhang, Shaowen Xie, Na Li, Lijian Xu. (2022) Tough, Self-Recoverable, Spiropyran (SP3) Bearing Polymer Beads Incorporated PAM Hydrogels with Sole Mechanochromic Behavior. Gels, 8 (4): (208).
2. Fan Chuyao, Deng Qiang, Zhu Ting F.. (2021) Bioorthogonal information storage in l-DNA with a high-fidelity mirror-image Pfu DNA polymerase. NATURE BIOTECHNOLOGY, 39 (12): (1548-1555).
3. Jia Tian, Chao Xiao, Baoxuan Huang, Chao Wang, Weian Zhang. (2020) Janus macromolecular brushes for synergistic cascade-amplified photodynamic therapy and enhanced chemotherapy. Acta Biomaterialia, 101 (495).
4. Jia Tian, Chao Xiao, Baoxuan Huang, Xiaoze Jiang, Hongliang Cao, Feng Liu, Weian Zhang. (2019) Combating Multidrug Resistance through an NIR-Triggered Cyanine-Containing Amphiphilic Block Copolymer. ACS Applied Bio Materials, 2 (5): (1862–1874).
5. Jinhao Yan, Haoqi Wang, Xueqin Zhao, Longxiang Tao, Xuefu Wang, Jun Yin. (2024) Polymorphic Supramolecular Therapeutic Platforms with Precise Dye/Drug Ratio to Perform Synergistic Chemo-Photo Anti-Tumor Therapy and Long-Term Immune Protection. Advanced Healthcare Materials, (2402907).

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