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DL-3-Aminoisobutyric acid

CAS No.
10569-72-9
Chemical Name:
DL-3-Aminoisobutyric acid
Synonyms
AIB;H-AIB-OH;3-Aminoisobutanoic acid;3-Aminoisobutyric acid;ANIB1;H-(ME)ALA-OH;H-ALA(ME)-OH;H-DL-3-AIB-OH;H-DL-AIB(3)-OH;H-DL-BETA-AIB-OH
CBNumber:
CB6673952
Molecular Formula:
C4H9NO2
Molecular Weight:
103.12
MDL Number:
MFCD00008145
MOL File:
10569-72-9.mol
MSDS File:
SDS
Last updated:2023-05-04 17:34:31

DL-3-Aminoisobutyric acid Properties

Melting point 179-182 °C(lit.)
Density 1.2300 (estimate)
refractive index 1.4650 (estimate)
storage temp. -20°C
solubility Methanol (Slightly), Water (Slightly)
form Solid
color White to Off-White
CAS DataBase Reference 10569-72-9(CAS DataBase Reference)
FDA UNII T68ALE2O9F
NIST Chemistry Reference DL-Beta-aminoisobutyric acid(10569-72-9)

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3
RTECS  AY7000000
NFPA 704
0
1 0

DL-3-Aminoisobutyric acid price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation CHM0029368 DL-3-AMINOISOBUTYRIC ACID 95.00% 10569-72-9 1G $721.57 2021-12-16 Buy
American Custom Chemicals Corporation CHM0029368 DL-3-AMINOISOBUTYRIC ACID 95.00% 10569-72-9 2.5G $983.88 2021-12-16 Buy
American Custom Chemicals Corporation CHM0029368 DL-3-AMINOISOBUTYRIC ACID 95.00% 10569-72-9 5G $1168.42 2021-12-16 Buy
Product number Packaging Price Buy
CHM0029368 1G $721.57 Buy
CHM0029368 2.5G $983.88 Buy
CHM0029368 5G $1168.42 Buy

DL-3-Aminoisobutyric acid Chemical Properties,Uses,Production

Uses

DL-3-Aminoisobutyric Acid is a useful compound for suppressing atherosclerosis in apolipoprotein E-knockout mouse.

Definition

ChEBI: 3-aminoisobutyric acid is a beta-amino-acid that is isobutyric acid in which one of the methyl hydrogens is substituted by an amino group. It has a role as a metabolite. It is functionally related to an isobutyric acid. It is a conjugate acid of a 3-aminoisobutyrate. It is a tautomer of a 3-aminoisobutanoic acid zwitterion.

Purification Methods

RS-β-Aminoisobutyric acid forms colourless prisms by crystallisation from hot H2O which are powdered and dried in vacuo. The purity is checked by paper chromatography (Whatman 1) using ninhydrin spray to visualise the amino acid; RF values in 95% MeOH and n-PrOH/5N HCOOH (8:2) are 0.36 and 0.50 respectively. [Kupiecki & Coon Biochemical Preparations 7 20 1960, Pollack J Am Chem Soc 65 1335 1943.] The R-enantiomer, isolated from iris bulbs or human urine, crystallises from H2O and sublimes in vacuo [Asen et al. J Biol Chem 234 343 1959]. The RS-hydrochloride crystallises from EtOH/Et2O with m 128-129o (also 130o) [B.hme et al. Chem Ber 92 1258, 1260, 1261 1959]. [Beilstein 4 III 1330.]

696-04-8
10569-72-9
Synthesis of DL-3-Aminoisobutyric acid from DIHYDROTHYMINE
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View Lastest Price from DL-3-Aminoisobutyric acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
DL-3-Aminoisobutyric acid pictures 2019-09-02 DL-3-Aminoisobutyric acid
10569-72-9
US $7.00 / KG 1KG 99% 1000KG Career Henan Chemical Co
DL-2-AMINO-ISO-BUTYRIC ACID DL-3-AMINO-2-METHYLPROPIONIC ACID DL-B-AMINOISOBUTYRIC ACID H-ALA(ME)-OH H-ALPHA-METHYLALANINE H-2-AMINOISOBUTYRIC ACID H-(ME)ALA-OH H-DL-MEALA(BETA)-OH H-DL-ALA-(NOCH2)OH H-DL-BETA-AIB-OH H-DL-3-AIB-OH H-DL-AIB(3)-OH H-DL-AIB(BETA)-OH 2-Methyl-beta-alanine Propanoic acid, 3-amino-2-methyl-, (.+/-.)- ALPHA-METHYLALANINE ALPHA-METHYL-BETA-ALANINE A-AMINO ISO-BUTYRIC ACID RARECHEM EM WB 0051 RARECHEM AK HD C017 (r,s)-3-amino-2-methylpropanoate 3-AMINO-2-METHYL-PROPIONIC ACID 2-(aminomethyl)propionic acid 3-Amino-2-methylpropanoate DL-3-AMINOISOBUTYRIC ACID /DL-SS-AMINOISOBUTYRIC ACID DL-B-AMINOISOBUTYRIC ACID CRYSTALLINE ANIB1 2-Methyl-b-alanine 3-Methyl-3-aminopropionic acid DL-3-Amino-2-methylpropanoic acid rac-(R*)-2-Methyl-3-aminopropionic acid DL-3-Aminoisobutyric acid,99% 3-aminoisobutyricaci DL-3-Aminoisobutyric acid USP/EP/BP H-AIB-OH 3-Aminoisobutyric acid AIB 3-Aminoisobutanoic acid 10569-72-9 62-57-5 C4H9NO2xH2O NH2CH2CHCH3COOH Peptide Synthesis Specialty Synthesis Unnatural Amino Acid Derivatives Alanine Derivatives Beta-Amino Acids Amino Acids Amino Acids