ChemicalBook >> CAS DataBase List >>DL-Threonine

DL-Threonine

CAS No.
80-68-2
Chemical Name:
DL-Threonine
Synonyms
THREONINE;H-DL-THR-OH;DL-Thr;DT 5621;DL-Thr-OH;DL-Threonin;Radish Seed;DL-Threoine;Bucladesina;DL-Theronine
CBNumber:
CB4475055
Molecular Formula:
C4H9NO3
Molecular Weight:
119.12
MDL Number:
MFCD00063722
MOL File:
80-68-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:23:11
Product description Number Pack Size Price
DL-Threonine ≥95% (titration) T8375 100g $397
DL-Threonine BioReagent, suitable for cell culture, suitable for insect cell culture T1520 100 g $327
DL-Threonine (contains DL-Allothreonine) >97.0%(T) T3105 100g $106
DL-Threonine (contains DL-Allothreonine) >97.0%(T) T3105 25g $39
DL-Threonine Asreported 289761 100g $337
More product size

DL-Threonine Properties

Melting point 244 °C (dec.)(lit.)
Boiling point 222.38°C (rough estimate)
alpha [α]D20 0±1.0゜ (c=6, H2O)
Density 1.3126 (rough estimate)
refractive index 1.4183 (estimate)
FLAVIS Number 17.021 | D,L-Threonine
storage temp. Store at RT.
solubility Soluble in water, Insoluble in absolute alcohol and oils
pka 2.09(at 25℃)
form Powder
color White
Water Solubility 200 g/L (25 ºC)
Merck 14,9380
BRN 1721647
Cosmetics Ingredients Functions HAIR CONDITIONING
HAIR WAVING OR STRAIGHTENING
ANTISTATIC
InChI 1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3+/m0/s1
InChIKey AYFVYJQAPQTCCC-STHAYSLISA-N
SMILES C[C@H](O)[C@@H](N)C(O)=O
LogP -1.136 (est)
CAS DataBase Reference 80-68-2(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII TFM6DU5S6A
NIST Chemistry Reference DL-Threonine(80-68-2)
EPA Substance Registry System Threonine (80-68-2)
UNSPSC Code 12352209
NACRES NA.75

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  24/25-37/39-26
WGK Germany  3
TSCA  TSCA listed
HS Code  29225000
NFPA 704
1
1 0

DL-Threonine price More Price(94)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich T8375 DL-Threonine ≥95% (titration) 80-68-2 100g $397 2026-04-30 Buy
Sigma-Aldrich T1520 DL-Threonine BioReagent, suitable for cell culture, suitable for insect cell culture 80-68-2 100 g $327 2026-04-30 Buy
TCI Chemical T3105 DL-Threonine (contains DL-Allothreonine) >97.0%(T) 80-68-2 100g $106 2026-04-30 Buy
TCI Chemical T3105 DL-Threonine (contains DL-Allothreonine) >97.0%(T) 80-68-2 25g $39 2026-04-30 Buy
Usbiological 289761 DL-Threonine Asreported 80-68-2 100g $337 2026-06-03 Buy
Product number Packaging Price Buy
T8375 100g $397 Buy
T1520 100 g $327 Buy
T3105 100g $106 Buy
T3105 25g $39 Buy
289761 100g $337 Buy

DL-Threonine Chemical Properties,Uses,Production

Chemical properties

Because of the 2 asymmetric carbon atoms contained in the threonine molecule there are D-threonine, L-threonine, D-doxylthreonine and L-doxylthreonine, four kinds of optical isomers, of which the amino acids constituting the protein is L-threonine while the other three optical isomers can not be used.
DL-threonine appears as white crystalline or crystalline powder, being odorless with slightly sweet taste. The melting point is about 245 ° C (decomposition). It can be dissolved in water (20.1g/100mL, 25 ° C), being insoluble in organic solvents such as ethanol. It has stable chemical property. Rats-intraperitoneally injection-LD50: 5.355 g/kg (type D).
L-threonine [72-19-5] has a melting point of about 256 ℃ (decomposition) with the physiological effect of the DL-type being 2 times of that of the DL-type. Rats subjecting to intraperitoneal injection has a LD50 of 3.094g/kg. The rest is the same as the DL type.

Uses

DL-Threonine is as an additive to animal feed. They are also used to chelate metal cations in order to improve the absorption of minerals from supplements, which may be required to improve the health or production of animals. This chelating ability is also used in fertilizers for agriculture.
DL-Threonine is an essential, non-protein amino acid naturally occurring in the human body and it is involved in many biological processes. DL-threonine takes part in the conversion of glycogen into the glucose pathway, supports muscle tissue maintenance and growth, and plays a key role in regulating levels of other amino acids.
L-threonine  is essential amino acids with the physiological effect of DL-threonine being half of that of the L-threonine. Upon its lack, people is easily susceptible to loss of appetite and fatty liver embolism. Threonine can not be de novo synthesized inside the higher animals body and must be supplied externally. The cereal protein, in addition to should being provided of L-lysine, should also be supplied with L-threonine. This is due to that although there is a high content of L-threonine, but the combination of threonine and peptide in the protein is difficult to be hydrolyzed and is not easily digested and absorbed. As a nutritional supplement, in order to play the best use of fruit, it can be co-used with glycine in the rice, co-used with glycine and valine in wheat flour, and co-used with glycine and methionine in the barley, oats as well as co-used with glycine and tryptophan in corn. Co-heating with hot grapes can easily produce empyreumatique and chocolate flavor with aromatherapy role. It can also be used for separation to obtain L-threonine and further for the preparation of amino acid infusion and integrated amino acid preparations.

Content analysis

It is the same as the content analysis method of "DL-alanine". Every mL of 0.1mol/L perchloric acid solution is equivalent to 11.91 mg of DL-threonine (C4H9NO3).

Toxicity

L-type: LD50: 26mmol/kg (rat, intraperitoneal injection); D-type: LD50 45mmol/kg (rat, intraperitoneal injection). It can be safely applied to food products (FDA, §172.320, 2000).

Description

Threonine (abbreviated as Thr or T) is an α-amino acid with the chemical formula HO2CCH(NH2)CH(OH)CH3. Its codons are ACU, ACA, ACC, and ACG. This essential amino acid is classified as polar. Together with serine, threonine is one of two proteinogenic amino acids bearing an alcohol group (tyrosine is not an alcohol but a phenol, since its hydroxyl group is bonded directly to an aromatic ring, giving it different acid/base and oxidative properties). It is also one of two common amino acids that bear a chiral side chain, along with isoleucine.
The threonine residue is susceptible to numerous posttr anslational modifications. The hydroxy side-chain can undergo Olinked glycosylation. In addition, threonine residues undergo phospho rylation through the action of a threonine kinase. In its phosphorylated form, it can be referred to as phospho threonine.

Chemical Properties

White crystalline powder

Occurrence

Foods high in threonine include cottage cheese, poultry, fish, meat, lentils, Black turtle bean and Sesame seeds.
Racemic threonine can be prepared from crotonic acid by alphafunctionalization using mercury (II) acetate.

History

Threonine was discovered as the last of the 20 common proteinogenic amino acids in the 1930s by William Cumming Rose.

Uses

DL-Threonine is used as a polar essential amino acid. It serves as a precursor of glycine as well as used in the biosynthesis of proteins. Further, it is used for biochemical research. In addition to this, it is used as a nutrition enhancer.

Definition

ChEBI: 2-amino-3-hydroxybutanoic acid is an alpha-amino acid that is butanoic acid substituted by an amino group at position 2 and a hydroxy group at position 3. It has a role as a plant metabolite.

brand name

L -Threonine is JAN.

Biosynthesis

As an essential amino acid, threonine is not synthesized in humans, hence we must ingest threonine in the form of threoninecontaining proteins. In plants and microorganisms, threonine is synthesized from aspartic acid via α-aspartyl-semialdehyde and homoserine. Homoserine undergoes O-phosphorylation; this phosphate ester undergoes hydrolysis concomitant with relocation of the OH group. Enzymes involved in a typical biosynthesis of threonine include :
aspartokinase
β-aspartate semialdehyde dehydrogenase
homoserine dehydrogenase
homoserine kinase
threonine synthase.

Synthesis Reference(s)

Tetrahedron Letters, 32, p. 1031, 1991 DOI: 10.1016/S0040-4039(00)74479-0
The Journal of Organic Chemistry, 63, p. 3499, 1998 DOI: 10.1021/jo9722717

Metabolism

Threonine is metabolized in two ways:
It is converted to pyruvate via threonine dehydrogenase. An intermediate in this pathway can undergo thiolysis with CoA to produce acetyl-CoA and glycine.
In humans, it is converted to α-ketobutyrate in a less common pathway via the enzyme serine dehydratase, and thereby enters the pathway leading to succinyl-CoA.
.

Stereoisomerism

Threonine is one of two proteinogenic amino acids with two chiral centers. Threonine can exist in four possible stereo isomers with the following configurations: (2S,3R), (2R,3S), (2S,3S) and (2R,3R). However, the name L-threonine is used for one single diastereomer, (2S,3R)-2-amino-3-hydroxybutanoic acid. The second stereoisomer (2S,3S), which is rarely present in nature, is called L-allo-threonine. The two stereo isomers (2R,3S)- and (2R,3R)-2-amino-3-hydroxy butanoic acid are only of minor importance.

References

[1] Patent: CN104892521, 2018, B. Location in patent: Paragraph 0069; 0070

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View Lastest Price from DL-Threonine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
DL-Threonine pictures 2026-06-05 DL-Threonine
80-68-2
1KG 98%min 500kgs WUHAN FORTUNA CHEMICAL CO., LTD
DL-Threonine pictures 2026-05-21 DL-Threonine
80-68-2
1KG 99% 200mt/year Jinan Finer Chemical Co., Ltd
DL-Threonine pictures 2025-05-23 DL-Threonine
80-68-2
$45.00 1kg 99% 20 tons Hebei Zhuanglai Chemical Trading Co Ltd
  • DL-Threonine pictures
  • DL-Threonine
    80-68-2
  • $0.00
  • 98%min
  • WUHAN FORTUNA CHEMICAL CO., LTD
  • DL-Threonine pictures
  • DL-Threonine
    80-68-2
  • $45.00
  • 99%
  • Hebei Zhuanglai Chemical Trading Co Ltd
H-DL-THR-OH DL-AMINO-HYDROXYBUTYRIC ACID DL-ALPHA-AMINO-BETA-HYDROXYBUTYRIC ACID ALLOTHREONINE, DL-(RG) THREONINE(allo-free), DL-(RG) DL-Threonin dl-tthreonine H-DL-Thr-OH (DL-Threonine) DL-THREONINE extrapure CHR DL-threonine, 99.5% rac-(R*)-2-[(S*)-1-Hydroxyethyl]glycine rac-Threonine A-AMINO-B-HYDROXYBUTYRIC ACID Radish Seed DL-Theronine DL-Threoine DL-Threonine (contains DL-Allothreonine) DL-Thr-OH DL-Threonine DL-Threonine (contains DL-Allothreonine) DL-2-AMINO-3-HYDROXYBUTANOIC ACID DL-2-AMINO-3-HYDROXYBUTYRIC ACID ALPHA-AMINO-BETA-HYDROXYBUTYRIC ACID DL-THREONINE (+/-)-2-AMINO-3-HYDROXYBUTYRIC ACID 2-AMINO-3-HYDROXYBUTYRIC ACID DL-Threonicne DL-Thr DL-Threonine≥ 99% (Titration) THREONINE, DL- (R*,S*)-2-AMINO-3-HYDROXYBUTYRIC ACID DL-THREONINE, FREE OF ALLOTHREONINE DL-THREONINE ALLO-FREE DL-THREONINE ALLO-FREE CELL CULTURE*TEST ED Dl-ThreonineForBiochemistry99+% DL-Threonine,99% DL-Threonine, 99.50% (n)-2-amino-3-hydroxybutyric acid DL-Threonine USP/EP/BP dextro,laevo-threonine (2S,3R)-rel-2-Amino-3-hydroxybutanoic acid DL-Threonine 80-68-2 DL-Threonine, for biochemistry Bucladesina DT 5621 Melatonin Impurity 15(Melatonin EP impurity A) DL-Threonine DL-Threonine, 98% DL-Threonine (Standard) THREONINE 80-68-2 72-19-5;80-68-2 CH3CHOHCHNH2COOH BioChemical Amino Acid Derivatives Amino Acids and Peptides Biochemicals and Reagents Amino Acids