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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 464생성일: 2026년 10월 25일

히푸르산

마뇨산 · 히푸르산 · 히푸릭애씨드 · BENZOYLGLYCINE · hippurate · hippuric · HIPURIC ACID · N-BENZOYLGLYCINE

https://huagongshe.com/ko/chemical/464

히푸르산 분자 구조식

식별자 및 물리적 특성

CAS No.495-69-2
분자식C9H9NO3
평균 분자량179.17 g/mol
단동위원소 질량179.05824315 g/mol
SMILESO=C(O)CNC(=O)c1ccccc1
InChIKeyQIAFMBKCNZACKA-UHFFFAOYSA-N
PubChem CID464
ChEMBLCHEMBL461
ChEBICHEBI:18089
EC No.207-806-3
DTXSIDDTXSID9046073
현지명히푸르산

화학 및 물리적 성질

XLogP0.3
극성 표면적66.4
수소 결합 공여자 수2
수소 결합 수용자 수3
회전 가능 결합 수3
무거운 원자 수13
형식 전하0
복잡도197
LogP(분배 계수)0.31
용해도3.75 mg/mL3.26g/L
녹는점187 - 191 °C187-191 °C (lit.)
증기압0.00000076 [mmHg]
Physical DescriptionSolid[Merck Index] White crystalline powder[Alfa Aesar MSDS]
Collision Cross Section139.72 Ų [M-H]- [CCS Type: DTMethod: single field calibrated with Agilent tune mix (Agilent)]142 Ų [M-H]- [CCS Type: DTMethod: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]149.6 Ų [M+Na]+ [CCS Type: DT146.82 Ų [M+H]+ [CCS Type: DTMethod: stepped-field]148.23 Ų [M-H]- [CCS Type: DT154.06 Ų [M+Na]+ [CCS Type: DT149.9 Ų [M+Na]+147.7 Ų [M-H]-153.1 Ų [M+Na]+145.9 Ų [M+H]+142.4 Ų [M-H]-
끓는 점311.69°C (rough estimate)
밀도1,371 g/cm3
굴절률1.5600 (estimate)
저장 조건Store below +30°C.
물리적 상태결정성 분말
pKa(산도 계수)3.62(at 25℃)
색상흰색에서 거의 흰색
pH2.5-3.5 (10g/l, H2O, 20℃)(slurry)
용해도물에 용해됩니다.
Merck14,4716
BRN1073987
안정성안정적인. 산화제와 호환되지 않습니다.
주요 응용임상 시험
화장품 원료 기능헤어 컨디셔닝
InChI1S/C9H9NO3/c11-8(12)6-10-9(13)7-4-2-1-3-5-7/h1-5H,6H2,(H,10,13)(H,11,12)
InChIKeyQIAFMBKCNZACKA-UHFFFAOYSA-N
SMILESOC(=O)CNC(=O)c1ccccc1
LogP(분배 계수)0.771
EPAGlycine, N-benzoyl- (495-69-2)

화학적 성질

White crystalline powder

안전 및 규제

GHS 분류This chemical does not meet GHS hazard criteria for 5.2% (3 of 58) of reports.DangerH302 (93.1%): Harmful if swallowed [Warning Acute toxicity, oral]H315 (94.8%): Causes skin irritation [Warning Skin corrosion/irritation]H318 (93.1%): Causes serious eye damage [Danger Serious eye damage/eye irritation]H335 (93.1%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposureRespiratory tract irritation]P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P354+P338, P317, P319, P321, P330, P332+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 58 reports by companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.Reported as not meeting GHS hazard criteria per 3 of 58 reports by companies.There are 7 notifications provided by 55 of 58 reports by companies with hazard statement code(s).Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
규제 정보Chemical: Glycine, N-benzoyl-Status: Active Update: 03-09-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/19668Glycine, N-benzoyl-: Does not have an individual approval but may be used under an appropriate group standard
기타 안전 정보Evaluation - Chemicals that are unlikely to require further regulation to manage risks to environment
유해성 요약The glycine conjugate of benzoic acid and a human metabolite of tolueneHas been measured in urine as an indicator of occupational exposure to toluene (in the absence of xylene and styrene exposure)[NIOSH Manual of Analytical Methods] May cause irritation[Alfa Aesar MSDS]
Hazard Classes and CategoriesAcute Tox. 4 (93.1%)Skin Irrit. 2 (94.8%)Eye Dam. 1 (93.1%)STOT SE 3 (93.1%)
TreatmentKidney dialysis is usually needed to relieve the symptoms of uremic syndrome until normal kidney function can be restored.
건강 영향Chronic exposure to uremic toxins can lead to a number of conditions including renal damage, chronic kidney disease and cardiovascular disease.
노출 경로Endogenous, Ingestion, Dermal (contact)
독성 요약Uremic toxins such as hippuric acid are actively transported into the kidneys via organic ion transporters (especially OAT3). Increased levels of uremic toxins can stimulate the production of reactive oxygen species. This seems to be mediated by the direct binding or inhibition by uremic toxins of the enzyme NADPH oxidase (especially NOX4 which is abundant in the kidneys and heart) (A7868). Reactive oxygen species can induce several different DNA methyltransferases (DNMTs) which are involved in the silencing of a protein known as KLOTHO. KLOTHO has been identified as having important roles in anti-aging, mineral metabolism, and vitamin D metabolism. A number of studies have indicated that KLOTHO mRNA and protein levels are reduced during acute or chronic kidney diseases in response to high local levels of reactive oxygen species (A7869).
Signs and SymptomsAs a uremic toxin, this compound can cause uremic syndrome. Uremic syndrome may affect any part of the body and can cause nausea, vomiting, loss of appetite, and weight loss. It can also cause changes in mental status, such as confusion, reduced awareness, agitation, psychosis, seizures, and coma. Abnormal bleeding, such as bleeding spontaneously or profusely from a very minor injury can also occur. Heart problems, such as an irregular heartbeat, inflammation in the sac that surrounds the heart (pericarditis), and increased pressure on the heart can be seen in patients with uremic syndrome. Shortness of breath from fluid buildup in the space between the lungs and the chest wall (pleural effusion) can also be present.
Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).
수질 위해 등급(WGK)3
TSCA 등재 상태TSCA listed
RTECS 번호MR8150000
관세 코드29242990
위험 문구(R)22-37/38-41-36/37/38
위험 표시Xn,Xi
안전 문구(S)26-39-36/37-22
위험 등급IRRITANT
기존화학 물질KE-02753
F 고인화성물질3-10
저장 분류11 - Combustible Solids

용도

용도

N-Benzoylglycine also known as Hippuric Acid is the glycine conjugate of benzoic acid commonly found in ruminant urine. It is synthesized in the liver and its production is greatly increased following consuption of benzoic acid. In itself it does not have a direct biological function, however p-hydroxy-hippurica acid can be used as an inhibitor of Ca2+ ATPase.

제조 및 합성 방법

제조 방법

Preparation of Hippuric acid from Glycine. Principle: The hydroxy and amino functions can be easily benzoylated using Benzoyl chloride in aqueous alkaline conditions. This reaction is known as Schotten-Baumann reaction. Reaction: Procedure: Dissolve 0.5 g of glycine in 5 ml of 10% NaOH solution in a 25 ml conical flask. Add 0.9 ml of benzoyl chloride in five portions to the solution. Stopper the flask and shake vigorously after each addition until all the benzoyl chloride is reacted. Transfer the solution to a beaker and add few grams of ice and add conc. HCl slowly with stirring until the solution is acidic to litmus paper. Filter the crystalline precipitate of the product on a Buchner funnel, wash with cold water and drain well. Place the solid in a conical flask with 10 ml CCl4 and boil gently for 10 min. Allow the mixture to cool slightly, filter under gentle suction and wash with 10-20 ml CCl4. Record the practical yield and re-crystallize it. Re-crystallization: Dissolve the crude product from boiling water (5 ml), with addition of decolorizing charcoal if necessary, filter the hot solution and cool the filtrate. The crystals of the product separate out. Filter, dry and record the melting point and TLC [using Butanal : acetic acid: water (4 : 1 : 1) as solvent or CHCl3:methanol (9 : 1) or toluene].

Hippuric Acid|Huagongshe