Basic Description

Synonyms	Z335244790 \| 2-Methylbenzyl alcohol, 98% \| AKOS000249529 \| Benzenemethanol, 2-methyl- \| NSC 91 \| A843387 \| Benzyl alcohol, o-methyl- (8CI) \| bmse000515 \| o-Tolyl carbinol \| SY013626 \| Q27268494 \| AI3-21536 \| alpha-Hydroxy-o-xylene \| o-Tolyl alcohol \| XPNG
Specifications & Purity	≥97%(GC)
Shipped In	Normal
Product Description	Product Application: 2-Methylbenzyl alcohol is widely used strong mobile phase additive in HPLC. it can be used to produce 2-methyl-benzaldehyde at temperature of 20Â°C. It will need reagent pyridinium chlorochromate with reaction time of 10 min.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Benzyl alcohols

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Benzyl alcohols
Intermediate Tree Nodes	Not available
Direct Parent	Benzyl alcohols
Alternative Parents	Toluenes Primary alcohols Hydrocarbon derivatives Aromatic alcohols
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Benzyl alcohol - Toluene - Organic oxygen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as benzyl alcohols. These are organic compounds containing the phenylmethanol substructure.
External Descriptors	methylbenzyl alcohol
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	488180235
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488180235
IUPAC Name	(2-methylphenyl)methanol
INCHI	InChI=1S/C8H10O/c1-7-4-2-3-5-8(7)6-9/h2-5,9H,6H2,1H3
InChIKey	XPNGNIFUDRPBFJ-UHFFFAOYSA-N
Smiles	CC1=CC=CC=C1CO
Isomeric SMILES	CC1=CC=CC=C1CO
WGK Germany	3
Molecular Weight	122.17
Beilstein	1929780
Reaxy-Rn	1929783
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1929783&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.

9 results found

Lot Number	Certificate Type	Date	Item
I2008213	Certificate of Analysis	Jul 16, 2024	M157901
H2318501	Certificate of Analysis	Jul 29, 2023	M157901
H2318502	Certificate of Analysis	Jul 29, 2023	M157901
K2224721	Certificate of Analysis	Nov 14, 2022	M157901
K2224722	Certificate of Analysis	Nov 14, 2022	M157901
K2224718	Certificate of Analysis	Nov 14, 2022	M157901
K2224716	Certificate of Analysis	Nov 14, 2022	M157901
K2224717	Certificate of Analysis	Nov 14, 2022	M157901
K2224720	Certificate of Analysis	Nov 14, 2022	M157901

Chemical and Physical Properties

Solubility	Soluble in methanol 0.1 g/mL.
Refractive Index	1.5408
Flash Point(°F)	219.2 °F
Flash Point(°C)	104°C
Boil Point(°C)	109-110°C
Melt Point(°C)	35-38°C
Molecular Weight	122.160 g/mol
XLogP3	1.600
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	122.073 Da
Monoisotopic Mass	122.073 Da
Topological Polar Surface Area	20.200 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	80.600
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. Xiangju Ye, Yinghao Chen, Yahui Wu, Xuemei Zhang, Xuchun Wang, Shifu Chen. (2019) Constructing a system for effective utilization of photogenerated electrons and holes: Photocatalytic selective transformation of aromatic alcohols to aromatic aldehydes and hydrogen evolution over Zn3In2S6 photocatalysts. APPLIED CATALYSIS B-ENVIRONMENTAL, 242 (302).
2. Qiang Zhang, Xiangyue Wei, Chengfeng Shen, Pengbo Ye, Wenli An, Xuehui Liu, Shimei Xu, Yu-Zhong Wang. (2024) Solvent-Regulated Tandem Oxidative Degradation of Polyethylene to Multifunctional Chemicals. ACS Sustainable Chemistry & Engineering, 12 (15): (5788-5798).

Solution Calculators

Molarity Calculator

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

Mass

=

Concentration

x

Volume

x

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)

x

Volume 1 (V1)

=

Concentration 2 (C2)

x

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

SKU	Size	Availability	Price
M157901-5g	5g	4	$9.90
M157901-25g	25g	2	$34.90
M157901-100g	100g	1	$123.90

2-Methylbenzyl Alcohol - >97.0%(GC), high purity , CAS No.89-95-2