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HCID 91508생성일: 2026년 10월 27일

알파-파이넨 옥사이드

알파-파이넨 옥사이드 · 3-Oxatricyclo[4.1.1.0(2,4)]octane, 2,7,7-trimethyl- · 2,7,7-trimethyl-3-oxatricyclo[4.1.1.02,4]octane · Nsc5609 · 2-pineneoxide · α-Epoxypinane · a-PineneOxide · AURORA KA-478

https://huagongshe.com/ko/chemical/91508

알파-파이넨 옥사이드 분자 구조식

식별자 및 물리적 특성

CAS No.1686-14-2
분자식C10H16O
평균 분자량152.23 g/mol
단동위원소 질량152.12011513 g/mol
SMILESCC1(C)C2CC3OC3(C)C1C2
InChIKeyNQFUSWIGRKFAHK-UHFFFAOYSA-N
PubChem CID91508
ChEMBLCHEMBL274511
ChEBICHEBI:29060
EC No.216-869-6
DTXSIDDTXSID5051781
현지명알파-파이넨 옥사이드

화학 및 물리적 성질

XLogP2.1
극성 표면적12.5
수소 결합 공여자 수0
수소 결합 수용자 수1
회전 가능 결합 수0
무거운 원자 수11
형식 전하0
복잡도221
SpringerMaterials PropertiesSchoenflies notation
LogP(분배 계수)2.01
Physical DescriptionSolid
끓는 점102-103 °C/50 mmHg (lit.)
밀도0.964 g/mL at 25 °C (lit.)
굴절률n20/D 1.469(lit.)
인화점150 °F
저장 조건Keep in dark place,Inert atmosphere,Room temperature
용해도클로로포름(적당), 디클로로메탄(적당), 에탄올(약간 용해됨)
물리적 상태기름
색상무색
비중0.97
헨리 상수2.3×10-2 mol/(m3Pa) at 25℃, Fichan et al. (1999)
안정성수분에 민감한
InChI1S/C10H16O/c1-9(2)6-4-7(9)10(3)8(5-6)11-10/h6-8H,4-5H2,1-3H3/t6-,7-,8,10/m1/s1
InChIKeyNQFUSWIGRKFAHK-BGPATTHWSA-N
SMILESCC1(C)[C@H]2CC3OC3(C)[C@@H]1C2
LogP(분배 계수)2.339 (est)
EPA3-Oxatricyclo[4.1.1.02,4]octane, 2,7,7-trimethyl- (1686-14-2)

안전 및 규제

GHS 분류This chemical does not meet GHS hazard criteria for 2.8% (1 of 36) of reports.WarningH302 (91.7%): Harmful if swallowed [Warning Acute toxicity, oral]P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 36 reports by companies from 5 notifications to the ECHA C&L Inventory.
규제 정보Chemical: 3-Oxatricyclo[4.1.1.02,4]octane, 2,7,7-trimethyl-REACH registered substance: 2,7,7-trimethyl-3-oxatricyclo[4.1.1.02,4]octane (EC: 216-869-6)3-Oxatricyclo4.1.1.02,4octane, 2,7,7-trimethyl-: Does not have an individual approval but may be used under an appropriate group standard
Hazard Classes and CategoriesAcute Tox. 4 (91.7%)
수질 위해 등급(WGK)3
TSCA 등재 상태TSCA listed
RTECS 번호TK4565000
운송 번호(UN)2810
관세 코드2910.90.9100
포장분류III
위험 등급6.1
기존화학 물질2000-3-1415
저장 분류10 - Combustible liquids

용도

용도

An industrially important reaction of optically active a-pinene oxide is rearrangement to campholene aldehyde (e.g., in the presence of zinc bromide). Subsequent aldol condensation with lower aliphatic aldehydes or ketones (e.g., propionaldehyde, butyraldehyde, or acetone) provides unsaturated aldehydes or ketones that can be reduced to the corresponding saturated alcohols. These are used in the fragrance industry as a sandalwood scent.

제조 및 합성 방법

제조 방법

a-Pinene oxide is prepared industrially by using percarboxylic acid. Processes based on air oxidation are also known.