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1004-23-5

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1004-23-5 Usage

General Description

4-Aminomethyl-phenol hydrochloride is a chemical compound commonly used in the manufacturing of hair dyes and colorants. It is a derivative of phenol and has the chemical formula C7H10ClNO. 4-Aminomethyl-phenol hydrochloride is used as a color precursor in oxidative hair dye formulations, where it reacts with hydrogen peroxide to produce the desired hair color. It also acts as a stabilizer and antioxidant in these formulations. Additionally, 4-Aminomethyl-phenol hydrochloride may have applications in other industries, such as in the synthesis of pharmaceuticals and other organic compounds. However, it is important to handle this chemical with care, as it can be harmful if swallowed, inhaled, or in contact with skin, and proper safety measures should be taken when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 1004-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1004-23:
(6*1)+(5*0)+(4*0)+(3*4)+(2*2)+(1*3)=25
25 % 10 = 5
So 1004-23-5 is a valid CAS Registry Number.

1004-23-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(aminomethyl)phenol,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-Hydroxybenzylamine hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1004-23-5 SDS

1004-23-5Relevant articles and documents

Neuroprotective principles from Gastrodia elata

Huang, Nai-Kuei,Chern, Yijuang,Fang, Jim-Min,Lin, Chia-I.,Chen, Wan-Ping,Lin, Yun-Lian

, p. 571 - 574 (2007)

Serum deprivation-induced neuronal-like PC12 cell apoptosis was used as an ischemic/hypoxic model to screen neuroprotective compounds from the rhizomes of Gastrodia elata, a traditional Chinese medicine. Two active compounds, bis(4-hydroxybenzyl)sulfide (

Fabrication of ω-Transaminase@Metal-Organic Framework Biocomposites for Efficiently Synthesizing Benzylamines and Pyridylmethylamines

Yu, Jinhai,Zong, Weilu,Ding, Yingying,Liu, Junzhong,Chen, Lina,Zhang, Hongjuan,Jiao, Qingcai

, p. 380 - 390 (2021/11/05)

In this study, ten ω-transaminases (ω-TAs) have been investigated to efficiently catalyze the synthesis of twenty-four functionalized benzylamines and pyridylmethylamines. We optimized the reactions, screened suitable amino donors and compared ω-transaminases activities for all aromatic aldehyde substrates. Under the optimized conditions, eighteen aromatic amines have been obtained with 60.4%–96.6% conversions and isolated only via simple extraction and recrystallization with 18.5%–81% yields on a preparative scale. Furthermore, we first immobilized the Bm-STA onto the MOFs via the physical adsorption to overcome the limitation of free enzyme and improve their industrial applications. The obtained Bm-STA/UiO-66-NH2 composites exhibited not only high enzymes loading (80.4 mg g?1) and enzyme activity recovery (95.8%), but also the better reusability, storage stability, pH stability and the tolerance to acetone and DMF.

1,2,3-Trimethoxypropane, a glycerol-based solvent with low toxicity: New utilization for the reduction of nitrile, nitro, ester, and acid functional groups with TMDS and a metal catalyst

Sutter, Marc,Pehlivan, Leyla,Lafon, Romain,Dayoub, Wissam,Raoul, Yann,Metay, Estelle,Lemaire, Marc

supporting information, p. 3020 - 3026 (2013/11/06)

1,2,3-Trimethoxypropane (1,2,3-TMP) was prepared from glycerol in one step in good yield and selectivity by phase transfer catalysis. According to OECD guidelines, a toxicity study was realized for this compound. It revealed that 1,2,3-TMP has a low acute toxicity, no skin sensitization, no mutagenicity and no ecotoxicity in an aquatic environment. This compound was also used as a solvent for the reduction of organic functions using either aluminium hydride or 1,1,3,3-tetramethyldisiloxane (TMDS) as a benign hydride source. In particular, a new process for the reduction of nitriles to amines in 2-MeTHF and in 1,2,3-TMP was developed, using TMDS in combination with copper triflate (Cu(OTf)2).

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