35249-89-9

Basic information

• Product Name: AMMONIUMGLYCOLATE
• Synonyms: 2-Hydroxyacetic acid ammonium salt;Acetic acid, hydroxy-, MonoaMMoniuM salt;Ammonium hydroxyacetate
• CAS NO: 35249-89-9
• Molecular Formula: C₂H₄O₃*H₃N
• Molecular Weight: 93.08
• Mol File: 35249-89-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 265.6°C at 760 mmHg
• Flash Point: 128.7°C
• Appearance: /
• Density: 0.99 at 20℃
• Vapor Pressure: 0.00125mmHg at 25°C
• CAS DataBase Reference: AMMONIUMGLYCOLATE(CAS DataBase Reference)
• NIST Chemistry Reference: AMMONIUMGLYCOLATE(35249-89-9)
• EPA Substance Registry System: AMMONIUMGLYCOLATE(35249-89-9)

Safety Data

• Hazardous Substances Data: 35249-89-9(Hazardous Substances Data)

Usage

General Description

AMMONIUMGLYCOLATE, also known as glycolic acid ammonium salt, is a chemical compound commonly used in hair care products as a hair straightening agent. It acts by breaking down the disulfide bonds in the hair, allowing it to be reshaped and straightened. It is also used as an ingredient in skin care products, where it works as an exfoliant to help remove dead skin cells and improve the overall texture and tone of the skin. AMMONIUMGLYCOLATE is a powerful ingredient and should be used with caution, as it can cause skin irritation and sensitivity in some individuals. It is important to follow the instructions and recommendations of the product when using this chemical.

InChI:InChI=1/C2H4O3.H3N/c3-1-2(4)5;/h3H,1H2,(H,4,5);1H3

Synthetic route

glycolic Acid (79-14-1) + ferric nitrate (Fe(NO3)3.9H2 O) + manganese nitrate Mn(NO3)2.6H2 O → ammonium glycolate (35249-89-9)

Conditions	Yield
In water

glycolic Acid (79-14-1) + ferric nitrate (7782-61-8) → ammonium glycolate (35249-89-9)

Conditions	Yield
With ammonium hydroxide In water

glycolic Acid (79-14-1) + ferric nitrate (Fe(NO3)3.9H2O) + manganese nitrate Mn(NO3)2.6H2O → ammonium glycolate (35249-89-9)

Conditions	Yield
In water

ammonia (7664-41-7) + sodium (7440-23-5) → ammonium glycolate (35249-89-9) + diammonium rhodizonate + glycolamide (598-42-5) + sodium glycolate (25289-18-3, 105938-46-3, 2836-32-0) + sodium rhodizonate dibasic (523-21-7)

Conditions	Yield
With carbon monoxide; ammonium chloride In ammonia adding NH4Cl before evapn. of NH3;

ammonium glycolate (35249-89-9) + uranyl ion (16637-16-4) → uranyl diglycolate

Conditions	Yield
In water loading of cation exchange resin (H(1+) form) with uranyl nitrate soln., elution with glycolate soln. (pH 5.0, 25°C); not isolated; IR spectroscopy;

ammonium glycolate (35249-89-9) + gadolinium(III) chloride (10138-52-0) → Gd(III) tris-glycolate

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate, 60°C;

ammonium glycolate (35249-89-9) + yttrium(III) chloride (10361-92-9) → glycolic acid ; yttrium(III)-compound

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate;

ammonium glycolate (35249-89-9) + thulium(III) chloride (13537-18-3) → Tm(3+)*3C2H3O3(1-)*2H2O=Tm(C2H3O3)3*2H2O

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate;

ammonium glycolate (35249-89-9) + erbium(III) chloride (10138-41-7) → erbium glycolate dihydrate

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate;

ammonium glycolate (35249-89-9) + ytterbium(III) chloride (10361-91-8) → Yb(3+)*3C2H3O3(1-)*2H2O=Yb(C2H3O3)3*2H2O

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate;

ammonium glycolate (35249-89-9) + lutetium(III) chloride (10099-66-8) → Lu(3+)*3C2H3O3(1-)*2H2O=Lu(C2H3O3)3*2H2O

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate;

ammonium glycolate (35249-89-9) + holmium(III) chloride (853560-92-6, 10138-62-2) → Ho(3+)*3C2H3O3(1-)*2H2O=Ho(C2H3O3)3*2H2O

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate;

ammonium glycolate (35249-89-9) + dysprosium(III) trichloride (10025-74-8) → Dy(3+)*3C2H3O3(1-)*2H2O=Dy(C2H3O3)3*2H2O

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate;

ammonium glycolate (35249-89-9) + gadolinium(III) chloride (10138-52-0) → glycolic acid ; gadolinium(III)-compound

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate, 25°C;

ammonium glycolate (35249-89-9) + terbium(III) chloride (10042-88-3) → Tb(3+)*3C2H3O3(1-)*2H2O=Tb(C2H3O3)3*2H2O

Conditions	Yield
In not given neutral soln., slight excess of ammonium glycolate;

Upstream product

• 107-16-4 glycolonitrile 
• 79-14-1 glycolic Acid 
• 7664-41-7 ammonia 
• 7440-23-5 sodium 
• 7782-61-8 ferric nitrate 
• 87-81-0 D-tagatose 
• 57-48-7 D-Fructose 
• 62147-49-3 1,3-dihydroxyacetone dimer 

Downstream Products

• 79-14-1 glycolic Acid 
• 96-35-5 glycolic acid methyl ester 
• 598-42-5 glycolamide 
• 33581-77-0 trimethylsilyl [(trimethylsilyl)oxy]acetate 

Relevant articles and documents

Oxidative degradation of reducing carbohydrates to ammonium formate with H2O2 and NH4OH

Oxidation of various carbohydrates into ammonium formate was investigated in the presence of hydrogen peroxide and ammonium hydroxide. Most of the examined carbohydrates except nonreducing sugars were efficiently converted into ammonium formate under envi

METHOD TO PRODUCE A CARBOXYLIC ACID ESTER FROM A CARBOXYLIC ACID AMMONIUM SALT BY ALCOHOLYSIS

The present invention relates to a method for obtaining a carboxylic acid ester from an aqueous solution of the corresponding carboxylic acid ammonium salt using alcoholysis. The recovered carboxylic acid ester may be subsequently hydrolyzed to produce the corresponding carboxylic acid.

Production of alcohols and olefins

A process for producing alcohols and olefins from a feedstream containing H2 and CO2 comprises using an iron carbide-based catalyst. A co-catalyst, for example copper, and/or a promoter, for example potassium, may also be present.