3130-75-4

3130-75-4 structure

Name: 4-(1,3-dioxo-1,3-dihydro-2h-isoindol-2-yl)butanoic acid
Chemical Name: 4-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl) butanoic acid
CAS Number: 3130-75-4
Molecular Formula: C₁₂H₁₁NO₄
Molecular Weight: 233.220
Catalog: Research Areas Inflammation/Immunology
Create Date: 2019-01-07 11:48:10
Modify Date: 2026-07-01 14:10:01
4-(N-Phthalimidoyl)butanoic acid (compound FB) is a hapten with a carboxyl group at the end of its spacer arm, suitable for reacting with free amine groups of proteins. 4-(N-Phthalimidoyl)butanoic acid can be combined with carrier proteins and used in antigen design[1].

Name	4-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl) butanoic acid
Synonyms	1,3-Dioxo-2-isoindolinebutyric acid 2H-Isoindole-2-butanoicacid, 1,3-dihydro-1,3-dioxo N-Phthaloyl γ-aminobutyric acid 4-(1,3-Dioxoisoindol-2-yl)butanoic acid O-Phthalimide-C3-acid 4-phthalimidobutyricacid 4-(1,3-DIOXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)BUTANOIC ACID 1,3-dioxo-2-isoindolinebutyricaci CBI-BB ZERO RECHEM AL CC 1,3-dihydro-1,3-dioxo-2h-isoindole-2-butanoicaci CHEMBRDG-BB 4-Phthalimidobutyric Acid OTAVA-BB BB0125160016 1,3-dihydro-1,3-dioxo-2h-isoindole-2-butanoicacid MFCD00196079 4-(Phthalimid-1-yl)butanoic acid 4-(1,3-dioxoisoindol-2-yl)butanoic acid 4-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)butanoic acid IFLAB-BB F1189-0010 1,3-Dioxo-1,3-dihydro-2H-isoindole-2-butyric acid 4-(1,3-Dihydro-1,3-dioxo-2H-isoindole-2-yl)butyric acid gamma-Phthalimido butyric acid N-PHTHALIMIDOBUTYRIC ACID 4-PhthalimidobutyricAcid> 4-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)butanoic acid 4-(1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-BUTYRIC ACID TIMTEC-BB SBB009239 4-phthalimidobuttersaure 4-(1,3-Dioxoisoindolin-2-yl)butanoic acid 4-Phthalimidobutanoic acid 1,3-Dioxoisoindoline-2-butanoic acid T-CHEM-BB B006361

Description	4-(N-Phthalimidoyl)butanoic acid (compound FB) is a hapten with a carboxyl group at the end of its spacer arm, suitable for reacting with free amine groups of proteins. 4-(N-Phthalimidoyl)butanoic acid can be combined with carrier proteins and used in antigen design[1].
Related Catalog	Research Areas >> Inflammation/Immunology
References	[1]. Mercader JV, et al. Development of monoclonal ELISAs for azinphos-methyl. 1. Hapten synthesis and antibody production. J Agric Food Chem. 1999 Mar;47(3):1276-84.

REFERENCE :: IJEBA6 Indian Journal of Experimental Biology. (Publications & Information Directorate, CSIR, Hillside Rd., New Delhi 110 012, India) V.1- 1963- Volume(issue)/page/year: 27,805,1989 ** REPRODUCTIVE DATA **

TOXIC EFFECTS :: Reproductive - Fertility - post-implantation mortality (e.g. dead and/or resorbed implants per total number of implants) Reproductive - Specific Developmental Abnormalities - other developmental abnormalities

REFERENCE :: PHARAT Pharmazie. (VEB Verlag Volk und Gesundheit, Neue Gruenstr. 18, Berlin DDR-1020, Ger. Dem. Rep.) V.1- 1946- Volume(issue)/page/year: 28,680,1973

Hazard Codes	Xi: Irritant;
HS Code	2925190090

HS Code	2925190090
Summary	2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%