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Terephthalaldehyde

CAS No.
623-27-8
Chemical Name:
Terephthalaldehyde
Synonyms
1,4-PHTHALALDEHYDE;Terephthaldehyde;1,4-BENZENEDICARBOXALDEHYDE;TEREPHTHALDICARBOXALDEHYDE;P-PHTHALALDEHYDE;TPAL;Benzene-1,4-dialdehyde;P-benzaldehyde;Terephtaldehyde;Terephthaladehyde
CBNumber:
CB1425781
Molecular Formula:
C8H6O2
Molecular Weight:
134.13
MDL Number:
MFCD00006949
MOL File:
623-27-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 23:37:07
Product description Number Pack Size Price
Terephthalaldehyde ReagentPlus , 99% T2207 5g $44.6
Terephthalaldehyde ReagentPlus , 99% T2207 100g $81.7
Terephthaldialdehyde for synthesis 8.08617 100g $86.1
Terephthalaldehyde >98.0%(GC) T0010 25g $34
Terephthalaldehyde >98.0%(GC) T0010 100g $102
More product size

Terephthalaldehyde Properties

Melting point 114-116 °C (lit.)
Boiling point 245-248 °C (lit.)
Density 1,06 g/cm3
vapor pressure 0.25-0.46Pa at 20-25℃
refractive index 1.4800 (estimate)
Flash point 76 °C
storage temp. Store below +30°C.
solubility 3g/l
form Crystalline Powder
color White to light yellow
Water Solubility 3 g/L (50 ºC)
Sensitive Air Sensitive
BRN 385863
Henry's Law Constant 1.6×101 mol/(m3Pa) at 25℃, Abraham and Jr. (2019)
Cosmetics Ingredients Functions PRESERVATIVE
InChI 1S/C8H6O2/c9-5-7-1-2-8(6-10)4-3-7/h1-6H
InChIKey KUCOHFSKRZZVRO-UHFFFAOYSA-N
SMILES [H]C(=O)c1ccc(cc1)C([H])=O
LogP 1 at 20.1℃ and pH6.6-6.8
CAS DataBase Reference 623-27-8(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII M2Y6E4N2TS
NIST Chemistry Reference 1,4-Benzenedicarboxaldehyde(623-27-8)
EPA Substance Registry System 1,4-Benzenedicarboxaldehyde (623-27-8)
UNSPSC Code 12352114
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xi
Risk Statements  36/37/38-36/37
Safety Statements  22-24/25-36-26-37/39
WGK Germany  1
RTECS  WZ0430000
Hazard Note  Irritant
TSCA  TSCA listed
HS Code  29122900
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Hazardous Substances Data 623-27-8(Hazardous Substances Data)
REACH Registrations Active
NFPA 704
1
2 0

Terephthalaldehyde price More Price(69)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich T2207 Terephthalaldehyde ReagentPlus , 99% 623-27-8 5g $44.6 2026-04-30 Buy
Sigma-Aldrich T2207 Terephthalaldehyde ReagentPlus , 99% 623-27-8 100g $81.7 2026-04-30 Buy
Sigma-Aldrich 8.08617 Terephthaldialdehyde for synthesis 623-27-8 100g $86.1 2026-04-30 Buy
TCI Chemical T0010 Terephthalaldehyde >98.0%(GC) 623-27-8 25g $34 2026-04-30 Buy
TCI Chemical T0010 Terephthalaldehyde >98.0%(GC) 623-27-8 100g $102 2026-04-30 Buy
Product number Packaging Price Buy
T2207 5g $44.6 Buy
T2207 100g $81.7 Buy
8.08617 100g $86.1 Buy
T0010 25g $34 Buy
T0010 100g $102 Buy

Terephthalaldehyde Chemical Properties,Uses,Production

Description

Terephthalaldehyde is an aromatic dialdehyde. Theoretically, the two aldehydes of terephthalaldehyde (TPA) are equivalent, so the single or double Schiff base from TPA and d-glucosamine (Glc) may be formed at the same time. It is used as an intermediate for the preparation of dyes and fluorescent whitening agents and in the synthesis of polyimines by reacting with aliphatic diamines. It is also used as a precursor for the preparation of paramagnetic microporous polymeric organic frameworks (POFs) through copolymerization with pyrrole, indole, and carbazole. As a good crosslinking agent, it could used in crosslinked chitosan hydrogel for the selective removal of anionic dyes[1].

Chemical Properties

WHITE TO LIGHT YELLOW CRYSTALLINE POWDER

Uses

Terephthalaldehyde (cas# 623-27-8) is a compound useful in organic synthesis.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 3, p. 788, 1955
Tetrahedron Letters, 36, p. 2285, 1995 DOI: 10.1016/0040-4039(95)00191-E

Synthesis

Using p-xylene, carbon tetrachloride, azodiisobutyronitrile and chlorine as raw materials and solvents, chlorination to obtain benzyl chloride, and then oxidized under the catalytic effect of nitric acid and zinc nitrate, the addition of zinc nitrate improves the yield of terephthalaldehyde to more than 89%, and the purity of the product is higher than 99.0%. Chlorination hydrolysis usually uses highly toxic chlorine gas directly, which is very unfriendly to the environment. In order to avoid the direct use of chlorine gas, N-fluorobenzenesulfonamide and sodium chloride were firstly used to react with p-xylene to synthesize p-dichlorobenzene in a highly selective way, and then the crude product of terephthalaldehyde was obtained through the catalytic action of 98% concentrated sulfuric acid and manganese dioxide, and finally the oxidized masterbatch was neutralized by sodium hydroxide and the finished product of terephthalaldehyde was obtained by recrystallization from the mixture of ethanol and water with the yield of terephthalaldehyde of 77% by weight.

Purification Methods

Terephthalaldehyde [623-27-8] M 134.1, m 116o, b 245 -248o/771mm. Crystallise terephthalaldehyde from water. [Beilstein 7 IV 2140.]

References

[1] Weng Q, et al. Controllable Synthesis and Biological Application of Schiff Bases from d-Glucosamine and Terephthalaldehyde. ACS Omega, 2020; 5: 24864–24870.

589-29-7
623-27-8
Synthesis of Terephthalaldehyde from 1,4-Benzenedimethanol
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View Lastest Price from Terephthalaldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Terephthalaldehyde pictures 2026-06-17 Terephthalaldehyde
623-27-8
1kg 98%min 10000kg WUHAN FORTUNA CHEMICAL CO., LTD
Terephthalaldehyde pictures 2026-06-16 Terephthalaldehyde
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0.99 RongNa Biotechnology Co.,Ltd
Terephthalaldehyde pictures 2026-05-28 Terephthalaldehyde
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$8.00 1KG 99% 10 ton Hebei Chuanghai Biotechnology Co,.LTD
TEREPHTHALALDEHYDE TEREPHTHALIC ALDEHYDE P-PHTHALICDICARBOXALDEHYDE 4-Formylbenzaldehyde p-Benzenedialdehyde p-Formylbenzaldehyde p-Phthaldialdehyde terephtaldehydes benzene-1,4dicarbaldehyde Terephthalaldehyde,98% p-Phenyldialdehyde P-PHTHALALDEHYDE=TEREPHTHALALDEHYDE Terephthalaldehyde 99% 4-PHTHALALDEHYDE p-phthalic aldehyde Terephthalaldehyde:Terephthaldicarbozaldehyde Terephthaldicarboxaldehyde, 98% 100GR Terephthaldicarboxaldehyde, 98% 5GR 1,4-Benzenedialdehyde 1,4-Diformylbenzene TEREPHTHALALDEHYDE/TEREPHTHALDICARBOXALDEHYDE/BENZENE-1,4-DICARBOXALDEHYDE GARLIC FLAKE Benzene-1,4-dicarboxaldehyde, Terephthaldicarboxaldehyde Terephthaldicarboxaldehyde,98% Benzene-1,4-Dicarboxaldehyde (1,4-Phthalaldehyde) Terephthalaldehyde,Benzene-1,4-dicarboxaldehyde, Terephthaldicarboxaldehyde 1,4-Dialdehydobenzene P-benzaldehyde 1,4-Terephthaldicarbaldehyde NSC 13395 p-DiforMylbenzene TEREPHTHALDIALDEHYDE FOR SYNTHESIS p-phthalaldehyd Two of benzene forMaldehyde Terephthalaldehyde ReagentPlus(R), 99% The benzene 2 forMaldehyde p-Phthaldehyde Terephthaldicarboxaldehyde white Terephthalaldehyde Vetec(TM) reagent grade, 98% 1,4-Phthalaldehydep-Phthaldehyde BENZENE-1,4-DICARBOXALDEHYDE 1,4-BENZENEDICARBALDEHYDE p-Phthalaldehdye Terephthalaldehyde,(Benzene-1,4-dicarboxaldehyde Terephthaldicarbo 4-Phthalaldehdye TEREPHTHALDICARBOXALDEHYDE 99% AKOS BBS-00004795 Terephthalaldehyde > Para-benzaldehyde 1,4-PHTHALALDEHYDE 623-27-8 Terephthalaldehyde ISO 9001:2015 REACH 1,4-Benzenedicarboxaldehyde (9CI, ACI) Terephthaldicarboxaldehyde、1,4-Phthalaldehyde、Benzene-1,4-dicarboxaldehyde Terephthaldicarbozaldehyde Benzene-1,4-dicarboxa Benzene-1,4-dialdehyde 1,4-PHTHALALDEHYDE