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1068-84-4

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1068-84-4 Usage

Uses

2-Aminomalonic Acid can be used in biological study of novel amino acid and metabolomics signature in mice overexpressing muscle uncoupling protein 3.

Definition

ChEBI: An amino dicarboxylic acid that is malonic acid in which one of the methylene hydrogens has been replaced by an amino group.

Check Digit Verification of cas no

The CAS Registry Mumber 1068-84-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1068-84:
(6*1)+(5*0)+(4*6)+(3*8)+(2*8)+(1*4)=74
74 % 10 = 4
So 1068-84-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H5NO4/c4-1(2(5)6)3(7)8/h1H,4H2,(H,5,6)(H,7,8)

1068-84-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name aminomalonic acid

1.2 Other means of identification

Product number -
Other names Aminomalonic acid

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:1068-84-4 SDS

1068-84-4Synthetic route

lead(II) 2-aminomalonate

lead(II) 2-aminomalonate

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With hydrogen sulfide In water35%
lead(II) 2-aminomalonate

lead(II) 2-aminomalonate

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With hydrogen sulfide; lead(II) bromide In water byproducts: lead(II) sulphide; to a suspn. of Pb-compd. containing PbBr2 H2S is passed through for 3 h.; PbS is filtered off and washed with distd. water, the filtrate is concd. under reduced pressure at 30°C, ppt. is collected by filtn. and washed with distd. water, elem. anal.;35%
chloromalonic acid
600-33-9

chloromalonic acid

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With methanol; ammonia
2-bromomalonic acid
600-31-7

2-bromomalonic acid

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With methanol; ammonia
2-aminopropanediamide
62009-47-6

2-aminopropanediamide

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With sodium hydroxide
2-nitromalonamide
69645-51-8

2-nitromalonamide

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With sodium amalgam; water
uramil
118-78-5

uramil

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With potassium hydroxide durch Kochen;
2-(phenylhydrazono)malonic acid
40885-82-3

2-(phenylhydrazono)malonic acid

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In ethanol
Aminomalonato(2-)-nickel(II)

Aminomalonato(2-)-nickel(II)

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With 2,6-dimethylpyridine; sodium nitrate at 25℃; Equilibrium constant;
L-serin
56-45-1

L-serin

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
In water at 10 - 20℃; Product distribution; Mechanism; electrolysis;
Glutamic acid
617-65-2

Glutamic acid

A

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

B

glycine
56-40-6

glycine

C

aspartic Acid
617-45-8

aspartic Acid

Conditions
ConditionsYield
In water Product distribution; oxidation pathway examined by argon arc plasma (40A, 10V);
D,L-threo-3-hydroxyaspartic acid
81601-40-3

D,L-threo-3-hydroxyaspartic acid

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
In water at 10 - 20℃; Product distribution; Mechanism; electrolysis;
rac-Ala-OH
302-72-7

rac-Ala-OH

A

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

B

serin
302-84-1

serin

C

2-amino-2-formylacetic acid
5735-66-0

2-amino-2-formylacetic acid

D

acetic acid
64-19-7

acetic acid

E

2-oxo-propionic acid
127-17-3

2-oxo-propionic acid

F

glycine
56-40-6

glycine

Conditions
ConditionsYield
In water Product distribution; oxidation pathway examined by argon arc plasma (40A, 10V);
DL-methionine
59-51-8

DL-methionine

A

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

B

cysteic acid
13100-82-8

cysteic acid

C

methionine sulfone
88547-35-7

methionine sulfone

E

glycine
56-40-6

glycine

F

aspartic Acid
617-45-8

aspartic Acid

Conditions
ConditionsYield
In water Product distribution; oxidation pathway examined by argon arc plasma (40A, 10V);
rac-Ala-OH
302-72-7

rac-Ala-OH

A

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

B

serin
302-84-1

serin

C

2-amino-2-formylacetic acid
5735-66-0

2-amino-2-formylacetic acid

Conditions
ConditionsYield
With town gas-O2 flame In water for 0.5h; Product distribution; various amino acids and aliphatic amines under different reaction conditions;
uramil
118-78-5

uramil

concentrated alkaline solution

concentrated alkaline solution

A

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

B

ureido-malonic acid

ureido-malonic acid

C

(2,4,6-trioxo-hexahydro-pyrimidin-5-yl)-urea
487-63-8

(2,4,6-trioxo-hexahydro-pyrimidin-5-yl)-urea

D

urea
57-13-6

urea

methanol
67-56-1

methanol

2-bromomalonic acid
600-31-7

2-bromomalonic acid

ammonia
7664-41-7

ammonia

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

isonitrosomalonate potassium

isonitrosomalonate potassium

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With sodium amalgam; water durch Reduktion;
chloromalonic acid
600-33-9

chloromalonic acid

methylalcoholic ammonia

methylalcoholic ammonia

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
at 45℃;
2-nitromalonamide
69645-51-8

2-nitromalonamide

water
7732-18-5

water

sodium amalgam

sodium amalgam

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

hydroxyimino-malonic acid ; dipotassium-salt

hydroxyimino-malonic acid ; dipotassium-salt

sodium amalgam

sodium amalgam

water

water

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

ISOPROPYL BENZYL ESTER.HCl

ISOPROPYL BENZYL ESTER.HCl

ISOPROPYL BENZYL ESTER

ISOPROPYL BENZYL ESTER

tert-butyl (1,3-dihydroxypropan-2-yl)carbamate
119881-02-6

tert-butyl (1,3-dihydroxypropan-2-yl)carbamate

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
With hydrogenchloride; hydrogen In palladium-carbon; dichloromethane
diethyl oximinomalonate
6829-41-0

diethyl oximinomalonate

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Conditions
ConditionsYield
Stage #1: diethyl oximinomalonate In methanol at 20℃;
Stage #2: With sodium tetrahydroborate; water; sodium hydroxide In methanol at 50 - 64℃;
2-aminomalonic acid
1068-84-4

2-aminomalonic acid

copper(II) nitrate

copper(II) nitrate

α-aminomalonato copper(II)

α-aminomalonato copper(II)

Conditions
ConditionsYield
under acidic conditions, narrow pH range;20%
2-aminomalonic acid
1068-84-4

2-aminomalonic acid

acetonedicarboxylic acid
473-90-5

acetonedicarboxylic acid

Conditions
ConditionsYield
With water; iodine
2-aminomalonic acid
1068-84-4

2-aminomalonic acid

A

methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

B

glycine
56-40-6

glycine

Conditions
ConditionsYield
beim Erhitzen auf den Schmelzpunkt;
2-aminomalonic acid
1068-84-4

2-aminomalonic acid

benzoyl chloride
98-88-4

benzoyl chloride

methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

2-aminomalonic acid
1068-84-4

2-aminomalonic acid

Aminomalonato(2-)-nickel(II)

Aminomalonato(2-)-nickel(II)

Conditions
ConditionsYield
With 2,6-dimethylpyridine; sodium nitrate; nickel(II) nitrate at 25℃; Equilibrium constant;
2-aminomalonic acid
1068-84-4

2-aminomalonic acid

acetic anhydride
108-24-7

acetic anhydride

A

2-acetylamino-3-methoxy-3-oxo-propyl acetate
55299-57-5

2-acetylamino-3-methoxy-3-oxo-propyl acetate

B

N-acetyl serine methyl ester
55299-56-4, 2311-26-4, 54322-41-7

N-acetyl serine methyl ester

C

4-carbomethoxy-2-hydroxy-2-methyl-1,3-oxazole

4-carbomethoxy-2-hydroxy-2-methyl-1,3-oxazole

Conditions
ConditionsYield
Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
2-aminomalonic acid
1068-84-4

2-aminomalonic acid

(1S)-(-)-camphanic chloride
39637-74-6

(1S)-(-)-camphanic chloride

(1'S,4'R)-(-)-N-camphanoyl<2-2H2>glycine

(1'S,4'R)-(-)-N-camphanoyl<2-2H2>glycine

Conditions
ConditionsYield
With pyridoxal 5'-phosphate; diothiothreitol Product distribution; multistep reaction: 1.) serine hydroxymethyltransferase, deuterated phosphate buffer (pD 6.0), 37 deg C, 1 h, 2.) toluene, 2 h; decarboxylation of 2-aminomalonic acid by serine hydroxymethyltransferase, stereospecificy, hydrogen exchange with solvent;
2-aminomalonic acid
1068-84-4

2-aminomalonic acid

glycine
56-40-6

glycine

Conditions
ConditionsYield
In water at 10 - 20℃; Product distribution; electrolysis;
In acetate buffer at 25℃; pH=5; Kinetics;

1068-84-4Related news

Detection and possible origins of Aminomalonic acid (cas 1068-84-4) in protein hydrolysates07/24/2019

Aminomalonic acid (Ama) was first detected in alkaline hydrolysates of proteins in 1984. In this work we describe our search for the origin of aminomalonic acid in alkaline hydrolysates of proteins. We have developed a technique for quantitation of aminomalonic acid based upon gas chromatography...detailed

1068-84-4Relevant articles and documents

Under-flame oxidation of amines and amino acids in an aqueous solution

Nomoto, Shinya,Shimoyama, Akira,Shiraishi, Susumu,Sahara, Denzo

, p. 1851 - 1855 (1996)

Flames from town gas-oxygen, hydrogen-oxygen, and ethylene-oxygen mixtures, when blown against the surface of an aqueous solution of amines and amino acids, induced an oxidation reaction in the aqueous phase, while an acetylene-oxygen flame failed to oxidize the compounds in solution. The hydrogen flame caused direct hydroxylation of the aromatic rings of phenylglycine homologs. The isomeric ratio of o-, m-, and p-hydroxyphenyl- amino acids produced was in accordance with that obtained by using the reaction systems of Fe2+-H2O2-EDTA and Fe2+-ascorbic acid-H2O2-EDTA, which are known to involve a hydroxyl radical as the agent for hydroxylating the aromatic rings. These results strongly suggest that the active species of flame-induced oxidation in an aqueous solution was the hydroxyl radical which was produced in the flames and extracted into the aqueous phase.

OXIDATIVE DEGRADATION OF HYDROXY AMINO ACIDS BY CONTACT GLOW DISCHARGE ELECTROLYSIS

Harada, Kaoru,Terasawa, Jun-ichi,Gunji, Hiromi

, p. 1545 - 1548 (1980)

Oxidative degradation of several hydroxy amino acids was carried out in order to confirm the reaction pathway of the oxidative degradation of β- and γ-amino acids by contact glow discharge electrolysis.The results indicate that the reaction products from hydroxy amino acids support the hypothesis that the oxidative degradation of β- and γ-amino acids pass through hydroxy amino acids.

-

Cassatt,J.C.,Wilkins,R.G.

, p. 6045 - 6050 (1968)

-

RENIN INHIBITORS IV

-

, (2008/06/13)

The invention concerns novel renin-inhibitory peptides which are useful for treating renin-assocated hypertension, hyperaldosteronism, and congestive heart failure. Processes for preparing the peptides, compositions containing them and methods of using them are included. Also included is a diagnostic method which uses the compounds to determine the presence of renin-associated hypertension or hyperaldosteronism.

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